Lediga jobb Valley Recruitment AB i Stockholm

Se alla lediga jobb från Valley Recruitment AB i Stockholm. Genom att välja ett specifikt yrke kan du även välja att se alla lediga jobb i Stockholm som finns inom det yrket.

Scientific Software Engineer - Data Analysis & Algorithms at Gnothis AB

Gnothis AB is seeking for a skilled Software Engineer who enjoys building experimental systems in a laboratory environment. This is a permanent position based at our HQ, located at the campus of Stockholm University (Stockholm, Sweden). Gnothis, founded in 2015 and supported by highly innovative industrial professionals and technology developers, is on a mission to develop a new frontier for single molecule DNA sequencing; to break the mold on how sequenci... Visa mer
Gnothis AB is seeking for a skilled Software Engineer who enjoys building experimental systems in a laboratory environment. This is a permanent position based at our HQ, located at the campus of Stockholm University (Stockholm, Sweden).
Gnothis, founded in 2015 and supported by highly innovative industrial professionals and technology developers, is on a mission to develop a new frontier for single molecule DNA sequencing; to break the mold on how sequencing is used as a clinical tool for the diagnosis of complex diseases. Gnothis technology integrates a wide range of cutting-edge sciences ranging from nanotechnology, photophysics, optics, surface chemistry, biochemistry and computational science.
Our instrumentation, software and analysis team currently consists of four engineers and we are now expanding the team as we scale development of the system.
We are seeking for an engineer with strong data analysis and scientific programming experience to develop our DNA sequencing data analysis pipeline. The role combines algorithm development, image analysis, and scientific data exploration, working closely with our instrumentation and biochemistry teams.
The work involves analyzing experimental data from our microscopy-based sequencing platform and developing the automated analysis pipeline that converts raw microscopy data into DNA sequencing results.
The position is part of a multidisciplinary team developing a prototype DNA sequencing instrument combining microscopy, microfluidics, nanofabrication and advanced data analysis.
Initial Project
The initial assignment will be to continuously analyze the latest experimental data from the lab in close collaboration with the biochemistry and instrument teams. This means developing new analysis algorithms, critically reviewing results together with the team, and driving experiment design to better address the research questions.
The work includes analyzing fluorescence microscopy data, developing algorithms for tasks such as peak detection and classification, and translating manual analysis workflows into automated pipelines using Python and Airflow. We are seeking for the right candidate who can make confident decisions based on previous experiences connected to laboratory environments (eg. development of diagnostic software tools and/or processing of fluorescence microscopy raw data).
Responsibilities

Develop algorithms and analysis methods for microscopy-based sequencing data


Implement automated analysis pipelines in Python and Airflow


Perform exploratory analysis of experimental datasets and extract meaningful insights


Collaborate closely with instrumentation and biochemistry teams to interpret results and improve experiments


Develop tools for data visualization, evaluation and reporting


Contribute to building a robust and scalable DNA sequencing analysis workflow.


Candidate Profile
For you to enjoy performing expected activities, and being a valuable member in an ambitious and innovative team; we think you are an engineer or scientist with strong experience in scientific programming and data analysis.
This role suits someone who enjoys working deeply with experimental datasets and extracting insight through algorithm development, statistical analysis and careful data interpretation.
The candidate should be comfortable working independently with complex datasets and driving the development of analysis methods in collaboration with a small multidisciplinary team.
Relevant backgrounds and skills include:

Master of Science and/or Ph.D educational background – ideally combined with a relevant Life Science focus.


Python programming for scientific computing


Image analysis and signal processing


Microscopy or fluorescence imaging data


Statistics and experimental data analysis


Scientific visualization and reporting


DNA sequencing or genomics data


A PhD with strong experience in microscopy data, sequencing data, or similar experimental datasets is highly preferred.
Gnothis offer a creative environment focused on technology and product development, a competitive compensation package and plenty of room for self-development as the company expands. This is a permanent position (not consultant assignment).
If above sounds like an exciting opportunity and you would like to hear more, do not hesitate and submit your application and we will get back to you!
Gnothis AB on LinkedIn: https://www.linkedin.com/company/gnothis/posts/?feedView=all
For inquires please email us at: markus.dahl@valleyrecruitment.se Visa mindre

Product Specialist – Diagnostics & Protein Chemistry (Stockholm)

The company, based in Stockholm, focuses on diagnostic-products within specific therapeutic areas connected to protein chemistry. The team is seeking a highly motivated and commercially oriented profile with previous solid experiences from biomedical and/or molecular biology field (eg. educational background such as BMA, Master of Science in biomedicine, molecular biology, microbiology, analytical chemistry, biochemistry or similar). This is a unique oppor... Visa mer
The company, based in Stockholm, focuses on diagnostic-products within specific therapeutic areas connected to protein chemistry. The team is seeking a highly motivated and commercially oriented profile with previous solid experiences from biomedical and/or molecular biology field (eg. educational background such as BMA, Master of Science in biomedicine, molecular biology, microbiology, analytical chemistry, biochemistry or similar). This is a unique opportunity (permanent position) to join a small and engaged team to work in a collaborative and positive atmosphere.
The appropriate candidate will report to the General Manager and will be responsible for the following duties:
Establish new accounts by organizing and planning daily work schedule to build on existing or potential sales outlets.
Develop lasting and tight relationships with laboratory clients, new and existing customers.
Identify and nurture potential sales opportunities.
Support installations and perform application-assays at the selected accounts.
Investigate problems; prepare reports, develop solutions and make recommendations to management to meet customers’ expectations.
Develop technical presentations and showcase the company's products to customers in clinical labs and research segments.
Study potentiality per account and forecast sales targets accordingly.
Gather current marketplace information on newly introduced products.
Prepare and conduct educational activities for specific assay and product customer solutions.
Provide historical records by keeping records on customer inquiries and sales.
Contribute to team efforts in accomplishing organizational goals.

Requirements – Knowledge, Skills, and Abilities – for the Position
Medical / science / pharmaceutical educational background
Previous experience working hands-on in Laboratory settings / Medical field
Valid driving license is a must.
Customer service oriented, with the ability to meet sales goals - Possess self-confidence, positive mentality, with the ability to manage territories effectively.
Reliable, hardworking, enthusiastic, with the ability to perform multiple assignments at the same time.
Fluent in both Swedish and English language

For questions regarding the company, team and products – reach out to Markus Dahl (markus.dahl@valleyrecruitment.se)
If you have a hands-on laboratory background, enjoy working in commercial environments and are seeking the next step in your career, do not hesitate and apply via the advert-link! Visa mindre

GMP-engineer for biotech company, Cellcolabs!

At Cellcolabs, we’re on a mission to democratize access to advanced cell therapies. As a biotech impact scale-up grounded in over two decades of research at Karolinska Institutet, we specialize in the large-scale production of Mesenchymal Stem Cells (MSCs) - cells known for their regenerative, immunomodulatory, and anti-inflammatory properties. From our GMP facility in Stockholm, we support clinical research targeting areas like cardiovascular disease, mus... Visa mer
At Cellcolabs, we’re on a mission to democratize access to advanced cell therapies. As a biotech impact scale-up grounded in over two decades of research at Karolinska Institutet, we specialize in the large-scale production of Mesenchymal Stem Cells (MSCs) - cells known for their regenerative, immunomodulatory, and anti-inflammatory properties.
From our GMP facility in Stockholm, we support clinical research targeting areas like cardiovascular disease, musculoskeletal injuries, and age-related degeneration. Now, we are looking for a hands-on GMP Engineer to help scale our production and bring the potential of cell therapy closer to patients.
This is a full-time, permanent position based at our Stockholm headquarters, with a 6-month probationary period.
Areas of responsibility
You’ll be part of a dedicated production team working in a GMP-grade cleanroom environment. Your daily responsibilities will include:
Manufacture advanced stem cell therapy products in accordance with GMP (B-grade environment).
Plan and execute routine tasks in daily production - hands-on stem-cell culture including routine preparations and related documentation
Be involved in document management, handling deviations, CAPA and change control errands, designing/updating working-instructions and qualification/validation work according to GMP-framework
Be involved in e.g. environmental monitoring sampling of the production premises
Be involved in storage and material management
Evaluate results and raw data
Be responsible for laboratory equipment and instruments, and assist service technicians when necessary

Qualifications
We value long-term collaboration and strive to create an environment where you can grow and thrive. To be successful in this position, you need the following qualifications:
Master/Bachelor degree within e.g. biotechnology,chemical engineering,molecular/cell biology or a related field
Experience in hands-on aseptic work connected to cell culture
Previous working experiences according to strict quality requirements and GMP
Proficiency in English

Experience working in a Grade B cleanroom environment is highly meritorious.
Who are you?
We’re looking for someone who is passionate about working hands-on with stem cells and motivated by the opportunity to make a meaningful impact on people's lives.
You bring a high level of quality awareness to your work, thrive in aseptic environments, and are structured, reliable, and detail-oriented. Strong communication and collaboration skills are essential, as is a proactive mindset — you actively contribute to a positive team culture, support your colleagues, and take initiative to improve workflows and solve challenges as they arise.
You’re comfortable navigating change and take pride in helping maintain a well-organized, efficient, and high-performing team.
Application
For this position and recruitment process, Cellcolabs is collaborating with Valley Recruitment AB.
If you find this opening interesting and would like to know more, do not hesitate to submit your application via the link below.
For questions regarding the role, please contact Markus Dahl directly via markus.dahl@valleyrecruitment.se
About Cellcolabs AB
Cellcolabs is a leading biotech impact scale-up on a mission to revolutionize healthcare through the large-scale production of Mesenchymal Stem Cells (MSCs). MSCs have shown great potential in preventing and treating a range of diseases and conditions. By scaling MSC production, we enable broader use in advanced therapies - paving the way for more widespread adoption in healthcare.
With 20 years of research from the Karolinska Institute as our foundation, Cellcolabs is approved for GMP production of Investigational Advanced Therapy Medicinal Products (IATMPs) by the Swedish Medical Products Agency. Backed by Sweden’s top health and life science entrepreneurs, along with impact investor Norrsken Launcher, we are headquartered in Stockholm, Sweden, and operate globally.
Read more at: http://cellcolabs.com Visa mindre

Scientist Biochemistry - Assay Development, Gnothis AB, Stockholm

Gnothis AB is seeking for a highly motivated scientist with strong focus on biochemistry and assay development. This is a permanent position based on the campus of Stockholm University, Stockholm Sweden. Gnothis, founded in 2015 and supported by highly innovative industrial professionals and technology developers, is on a mission to develop a new frontier for single molecule DNA sequencing; to break the mold on how sequencing is used as a clinical tool for... Visa mer
Gnothis AB is seeking for a highly motivated scientist with strong focus on biochemistry and assay development. This is a permanent position based on the campus of Stockholm University, Stockholm Sweden.
Gnothis, founded in 2015 and supported by highly innovative industrial professionals and technology developers, is on a mission to develop a new frontier for single molecule DNA sequencing; to break the mold on how sequencing is used as a clinical tool for the diagnosis of complex diseases. Gnothis technology integrates a wide range of cutting-edge sciences ranging from nanotechnology, photophysics, optics, surface chemistry, biochemistry and computational science.
The company has taken significant steps forward, and for the right person this is a unique opportunity to join a focused and dedicated team with a passion for developing a new world-class technology platform!
Responsibilities:
Develop protocols and methods for functionalization of Gnothis sequencing chip.
Plan and execute laboratory work in accordance with set project plans.
Accurately analyze and present data to support project decisions and milestones.
Participate in meetings and project planning.
Collaborate with cross-functional team members (bioinformaticians, chemists, physicists).
Participate in routine lab maintenance activities

Qualifications:
PhD degree in molecular biology, biochemistry, biotechnology or related field with 2-3 years of industrial experience in product development.
Extensive scientific and technical knowledge in molecular biology and biochemistry.
Experience with assay development within DNA sequencing and amplification technology.
Background in protein engineering and labeling methods.
Experience of bio-chip prototyping with integrated fluidics is a plus.
Ability to plan and execute to clear timelines and to prioritize tasks.
Ability both to work independently and to actively collaborate within and across teams.
Fluent written and spoken English, and excellent communication skills.

This is a permanent position (not consultant assignment) based on the campus of Stockholm University, Stockholm, Sweden.
Gnothis offer a creative environment focused on technology and product development, a competitive compensation package and plenty of room for self-development as the company expands.
If above sounds like an exciting opportunity and you would like to hear more, do not hesitate and submit your application and we will get back to you!
For inquires please email us at: markus.dahl@valleyrecruitment.se Visa mindre

GMP-engineer for biotech company, Cellcolabs!

At Cellcolabs, we’re on a mission to democratize access to advanced cell therapies. As a biotech impact scale-up grounded in over two decades of research at Karolinska Institutet, we specialize in the large-scale production of Mesenchymal Stem Cells (MSCs) - cells known for their regenerative, immunomodulatory, and anti-inflammatory properties. From our GMP facility in Stockholm, we support clinical research targeting areas like cardiovascular disease, mus... Visa mer
At Cellcolabs, we’re on a mission to democratize access to advanced cell therapies. As a biotech impact scale-up grounded in over two decades of research at Karolinska Institutet, we specialize in the large-scale production of Mesenchymal Stem Cells (MSCs) - cells known for their regenerative, immunomodulatory, and anti-inflammatory properties.
From our GMP facility in Stockholm, we support clinical research targeting areas like cardiovascular disease, musculoskeletal injuries, and age-related degeneration. Now, we are looking for a hands-on GMP Engineer to help scale our production and bring the potential of cell therapy closer to patients.
This is a full-time, permanent position based at our Stockholm headquarters, with a 6-month probationary period.
Areas of responsibility
You’ll be part of a dedicated production team working in a GMP-grade cleanroom environment. Your daily responsibilities will include:
Manufacture advanced stem cell therapy products in accordance with GMP (B-grade environment).
Plan and execute routine tasks in daily production - hands-on stem-cell culture including routine preparations and related documentation
Be involved in document management, handling deviations, CAPA and change control errands, designing/updating working-instructions and qualification/validation work according to GMP-framework
Be involved in e.g. environmental monitoring sampling of the production premises
Be involved in storage and material management
Evaluate results and raw data
Be responsible for laboratory equipment and instruments, and assist service technicians when necessary

Qualifications
We value long-term collaboration and strive to create an environment where you can grow and thrive. To be successful in this position, you need the following qualifications:
Master/Bachelor degree within e.g. biotechnology,chemical engineering,molecular/cell biology or a related field
Experience in hands-on aseptic work connected to cell culture
Previous working experiences according to strict quality requirements and GMP
Proficiency in English

Experience working in a Grade B cleanroom environment is highly meritorious.
Who are you?
We’re looking for someone who is passionate about working hands-on with stem cells and motivated by the opportunity to make a meaningful impact on people's lives.
You bring a high level of quality awareness to your work, thrive in aseptic environments, and are structured, reliable, and detail-oriented. Strong communication and collaboration skills are essential, as is a proactive mindset — you actively contribute to a positive team culture, support your colleagues, and take initiative to improve workflows and solve challenges as they arise.
You’re comfortable navigating change and take pride in helping maintain a well-organized, efficient, and high-performing team.
Application
For this position and recruitment process, Cellcolabs is collaborating with Valley Recruitment AB.
If you find this opening interesting and would like to know more, do not hesitate to submit your application via the link below.
For questions regarding the role, please contact Markus Dahl directly via markus.dahl@valleyrecruitment.se
About Cellcolabs AB
Cellcolabs is a leading biotech impact scale-up on a mission to revolutionize healthcare through the large-scale production of Mesenchymal Stem Cells (MSCs). MSCs have shown great potential in preventing and treating a range of diseases and conditions. By scaling MSC production, we enable broader use in advanced therapies - paving the way for more widespread adoption in healthcare.
With 20 years of research from the Karolinska Institute as our foundation, Cellcolabs is approved for GMP production of Investigational Advanced Therapy Medicinal Products (IATMPs) by the Swedish Medical Products Agency. Backed by Sweden’s top health and life science entrepreneurs, along with impact investor Norrsken Launcher, we are headquartered in Stockholm, Sweden, and operate globally.
Read more at: http://cellcolabs.com Visa mindre

Senior Scientist – Organic and Surface Chemistry, Gnothis AB, Stockholm

Ansök    Maj 23    Valley Recruitment AB    Organisk kemist
Gnothis AB is now seeking for a highly motivated scientist within surface chemistry. This is a permanent position based on the campus of Stockholm University, Stockholm Sweden. Gnothis, founded in 2015 and supported by highly innovative industrial professionals and technology developers, is on a mission to develop a new frontier for single molecule DNA sequencing; to break the mold on how sequencing is used as a clinical tool for the diagnosis of complex ... Visa mer
Gnothis AB is now seeking for a highly motivated scientist within surface chemistry.
This is a permanent position based on the campus of Stockholm University, Stockholm Sweden.
Gnothis, founded in 2015 and supported by highly innovative industrial professionals and technology developers, is on a mission to develop a new frontier for single molecule DNA sequencing; to break the mold on how sequencing is used as a clinical tool for the diagnosis of complex diseases. Gnothis technology integrates a wide range of cutting-edge sciences ranging from nanotechnology, photophysics, optics, surface chemistry, biochemistry and computational science.
The company has taken significant steps forward, and for the right person this is a unique opportunity to join a focused and dedicated team with a passion for developing a new world-class technology platform!
Role description:
You will be a part of an R&D team to develop protocols and methods for chemical functionalization of Gnothis sequencing chip. Your aim is to take on R&D responsibility for Gnothis surface chemistry, but at the same time you also enjoy working with the team to solve technical challenges within a much wider range of scientific fields. As a key member of Gnothis R&D team you will be involved in all stages of product development, from concept design to realized product. Responsibilities will include planning for projects, designing and executing your own experiments, and analyzing results to support project decisions and milestones.
Qualifications:
To fit the role, you have a PhD (or comparable industrial experience) in organic chemistry, surface chemistry, material science or other relevant scientific discipline.
Extensive experience of glass and metal functionalization chemistries.
Demonstrated expertise in surface plasmon resonance (SPR)
Experience of bio-chip prototyping with integrated fluidics.
Expertise in molecular DNA technology, sequencing, oligonucleotides and DNA polymerases (optional).
Ability to plan and execute to clear timelines and to prioritize tasks.
Ability both to work independently and to actively collaborate within and across teams.
Fluent written and spoken English and excellent communication skills.

This is a permanent position (not consultant assignment) based on the campus of Stockholm University, Stockholm, Sweden.
Gnothis offer a creative environment focused on technology and product development, a competitive compensation package and plenty of room for self-development as the company expands.
If above sounds like an exciting opportunity and you would like to hear more, do not hesitate and submit your application and we will get back to you!
For inquires please email us at: markus.dahl@valleyrecruitment.se Visa mindre

Manufacturing Engineer (stem-cell products), Procella Therapeutics AB

At Procella Therapeutics (part of Smartcella Holding AB) we provide advanced capabilities within stem cell therapy development and have inhouse cGMP manufacturing. We have globally licensed cardiac stem cell therapy in clinical stages (in strong collaboration with AstraZeneca) and a growing pipeline of life changing stem cell therapies. We are now seeking motivated Manufacturing Engineers, for permanent positions, to join the growing on-site manufacturing ... Visa mer
At Procella Therapeutics (part of Smartcella Holding AB) we provide advanced capabilities within stem cell therapy development and have inhouse cGMP manufacturing. We have globally licensed cardiac stem cell therapy in clinical stages (in strong collaboration with AstraZeneca) and a growing pipeline of life changing stem cell therapies.
We are now seeking motivated Manufacturing Engineers, for permanent positions, to join the growing on-site manufacturing team in Tullinge, Stockholm.
About The Position
As Manufacturing Engineer you will be responsible for producing stem-cells for clinical and commercial use. You will be part of a great team with high competence, and you will be working at a patient-focused, growing, and developing company that makes a difference. This role will work closely with cross-functional teams internally (process development, analytical development, quality and regulatory). Reporting to the Head of Manufacturing & GMP Facilities, this full-time position is located at Procella Headquarters in Tullinge, Stockholm.
Responsibilities
Support the daily activities in the laboratory and GMP facility
Support cross-functional activities related to manufacturing and process development
Manufacturing of drug substances and drug products for clinical and future commercial use in accordance with regulatory requirements
Execute GMP processes according to production schedules and instructions (e.g., MBR, SOP, and work instructions). The work includes some weekend work and on-call duty.
Comply with company policies and standards, risk assessments, instructions, and protocols to produce stem cells batches
Prepare, review, and revise GMP documentation
Participate in tech transfer activities
Coordinate periodic calibration, and maintenance and act as a superuser for equipment and instruments
Handling CAPA and initiation of deviation
Supervise and train team members in cleanroom environments

Skills
Ability to work in clean room environments using a good aseptic technique (eg. grade B (A) and in BSC)
Good understanding and application of GMP and regulatory requirements.
Experience working in GMP for clinical or commercial use
Good understanding of biological pharmaceutical manufacturing
Experience with small scale (manual handling) of cell culture in clean room environments is an asset

Qualifications
MSc/BSc in Life science or relevant areas is preferred
Experience of working in a regulated environment, ideally with upstream and/or downstream processes
You understand biological manufacturing and testing (R&D and clinical manufacturing)
You have at least 3 years of experience in the pharmaceutical industry, preferably in biopharmaceuticals
Extensive GMP knowledge and experience

Personal attributes
You are ambitious and able to work independently. You like to take initiatives and perform your activities with high accuracy using a quality-oriented mindset. You are a natural leader who thrives in a role where communication and collaboration are in focus. You can create and maintain rewarding working relationships both externally and internally.
This is a unique opportunity and you will be part of a great organization within the SmartCella group. Initial focus is to act hands-on to produce life changing products according to critical quality standards. As the business grows there will be great opportunities for personal development and to take on new exciting projects/roles. You will receive a competitive compensation package including pension-, health covering- and insurance plans including a competitive monthly salary. We welcome, and support diversity and are very proud to be a multicultural workplace. We have an open and transparent working environment and encourage collaboration, where inclusion are important values for us.
Submit your application today! We will review applications on an ongoing basis and hope to fill the position as soon as possible.
Reach out to Markus at markus.dahl@valleyrecruitment.se for questions regarding both the position and company.
About the company
SmartCella is a world-leading biotech & medtech company pioneering the future of targeted therapies by combining first-in-class delivery platforms with cutting-edge cell and gene therapies. The SmartCella group consist of SmartCella Holding AB, ProCella Therapeutics AB, SmartWise AB and SmartCella Solutions AB with a total of 65 employees from more than 20 nationalities.
Homepage: https://www.smartcella.com/procella/ Visa mindre

Scientist Quality Control – Analytical Chemistry, Gnothis AB, Stockholm

Ansök    Feb 16    Valley Recruitment AB    Analytisk kemist
Gnothis is expanding and is now aiming strengthening the team with a Quality Control Scientist with a strong background in analytical chemistry. Gnothis, founded in 2015 and supported by highly innovative industrial professionals and technology developers, is on a mission to develop a new frontier for single molecule DNA sequencing; to break the mold on how sequencing is used as a clinical tool for the diagnosis of complex diseases. Gnothis technology int... Visa mer
Gnothis is expanding and is now aiming strengthening the team with a Quality Control Scientist with a strong background in analytical chemistry.

Gnothis, founded in 2015 and supported by highly innovative industrial professionals and technology developers, is on a mission to develop a new frontier for single molecule DNA sequencing; to break the mold on how sequencing is used as a clinical tool for the diagnosis of complex diseases. Gnothis technology integrates a wide range of cutting-edge sciences ranging from nanotechnology, photophysics, optics, surface chemistry, biochemistry and computational science.

The company has taken significant steps forward, and for the right person this is a unique opportunity to join a focused and dedicated team with a passion for developing a new world-class technology platform!

Job description

- You will be responsible for the synthesis, purification, validation, and stability testing of chemicals used for DNA sequencing; in particular HPLC purification of labeled nucleotide molecules and validation of such purification workflows by mass spectrometry.

- The role will also require you to formulate procedures and perform quality control testing of a wide range of chemicals, e.g. buffers, nucleotides and proteins.

To perform well in the role, we think you have:

- A Master of Science and a PhD degree (or comparable industrial experience) in analytical chemistry or similar scientific discipline.

- Excellent analytical and problem-solving skills with a proactive approach, along with an interest in identifying, investigating, and solving technical challenges.

- Fluent written and spoken English and excellent communication skills.

- Solid experience of laboratory work, and you enjoy working hands-on in a laboratory setting.

- Solid experiences working in high performing teams in dynamic working environments.

- A positive and goal-oriented mindset together with a calm and pragmatic approach to challenging situations.

Ideally you have:

- Industrial experience working with custom synthesis/production projects with extensive knowledge and experience of analytical chemistry workflows and instruments.

- Experience of LIMS data systems for chemical inventory.

- Experience of molecular biochemistry, working with DNA and proteins.

- Experience of NHS ester conjugation chemistry.

This is a permanent position (not consultant assignment) based on the campus of Stockholm University, Stockholm, Sweden.

Gnothis offer a creative environment focused on technology and product development, a competitive compensation package and plenty of room for self-development as the company expands.

If above sounds like an exciting opportunity and you would like to hear more, do not hesitate and submit your application and we will get back to you!

For inquires please email us at: markus.dahl@valleyrecruitment.se Visa mindre

Scientist Quality Control – Analytical Chemistry, Gnothis AB, Stockholm

Gnothis is now seeking for a Quality Control Scientist with a strong background in analytical chemistry. Gnothis, founded in 2015 and supported by highly innovative, competent and successful industrial professionals and technology developers, is on a mission to develop a new frontier for single molecule DNA sequencing; to break the mold on how sequencing is used as a clinical tool for the diagnosis of complex diseases. Gnothis technology integrates a wide... Visa mer
Gnothis is now seeking for a Quality Control Scientist with a strong background in analytical chemistry.

Gnothis, founded in 2015 and supported by highly innovative, competent and successful industrial professionals and technology developers, is on a mission to develop a new frontier for single molecule DNA sequencing; to break the mold on how sequencing is used as a clinical tool for the diagnosis of complex diseases. Gnothis technology integrates a wide range of cutting-edge sciences ranging from nanotechnology, photophysics, optics, surface chemistry, biochemistry and computational science.

For the right person this is an opportunity to join a focused and dedicated team with a passion for developing a new world-class technology platform!

Job description

- As quality control scientist you will be responsible for the organization, procurement (or synthesis), purity and stability testing of chemicals and reagents involved in Gnothis sequencing workflow.

- The ideal applicant is one that is highly organized, well versed in analytical chemistry tools and have experience of chemical inventory work.

- The role will require you to formulate procedures and perform quality control testing of a wide range of chemicals, e.g. buffers, nucleotides and proteins.

Qualification

- To fit the role, you have a Master of Science and a PhD (or comparable industrial experience) in analytical chemistry or similar scientific discipline.

- As a person you are a self-motivated scientist who finds joy in structure and order. You lead by example and have a hands-on mentality.

- You have extensive experience of analytical chemistry tools; not only to run analyses of reagents, e.g, by HPLC and MS, but also to interpret the results and understand the molecular state of the analytes.

- You have excellent analytical and problem-solving skills with a proactive approach, along with an interest in identifying, investigating, and solving technical challenges.

- Fluent written and spoken English and excellent communication skills is a requirement.

- It is important that you have experience of laboratory work and enjoy working in a laboratory. You ought to feel comfortable and be productive in a dynamic working environment. As an R&D team member you have a calm and pragmatic approach to challenging situations and are friendly and positive to work with.

Ideally you have:

- Extensive knowledge and experience of analytical chemistry workflows and instruments.

- Experience of LIMS data systems for chemical inventory.

- Experience of molecular biochemistry, working with DNA and proteins.

- Experience of NHS ester conjugation chemistry.

This is a permanent position based on the campus of Stockholm University, Stockholm, Sweden.

We offer a creative environment focused on technology and product development, a competitive compensation and plenty of room of self-development as the company expands.

If above sounds like an exciting opportunity and you would like to hear more, do not hesitate and submit your application and we will get back to you!

For inquires please email us at: markus.dahl@valleyrecruitment.se Visa mindre

Scientist Biochemistry, Gnothis AB, Stockholm

Ansök    Maj 17    Valley Recruitment AB    Biokemist
Gnothis is now seeking for a Scientist with a strong focus on biochemistry and assay development. Gnothis is on a mission to develop a new frontier for single molecule DNA sequencing; to break the mold on how sequencing is used as a clinical tool for the diagnosis of complex diseases. The company was founded in 2015 and is supported by highly innovative and successful industrial professionals and technology developers. Gnothis technology integrates a wide... Visa mer
Gnothis is now seeking for a Scientist with a strong focus on biochemistry and assay development.

Gnothis is on a mission to develop a new frontier for single molecule DNA sequencing; to break the mold on how sequencing is used as a clinical tool for the diagnosis of complex diseases. The company was founded in 2015 and is supported by highly innovative and successful industrial professionals and technology developers. Gnothis technology integrates a wide range of cutting-edge sciences ranging from nanotechnology, photophysics, optics, surface chemistry, biochemistry and computational science. The innovative company is on a journey to further develop and commercialize the product with final aim to make a difference for patients.

For the right person this is an opportunity to join a focused and dedicated team with a passion for developing a new world-class technology platform!

Job description

- As a scientist within biochemistry, you are responsible for planning and executing experiments connected to assay/application development.

- The ideal applicant is one that is highly organized, well versed in biochemical tools and assays and is driven by hands-on laboratory-based work.

- The role will require you to work and coordinate laboratory experiments with R&D team members.

Qualifications

- To fit the role, you have a Master of Science and a PhD in biochemistry/molecular biology/biomedicine or similar scientific discipline.

- It is crucial that you have extensive experience of hands-on laboratory work.

- As a person you are a self-motivated, take your own initiatives, have a hands-on mentality and perform your work with a high-quality mindset.

- You have excellent analytical and problem-solving skills with a proactive approach, along with an interest in identifying, investigating, and solving biochemical and technical challenges.

- As an R&D team member you have a calm and pragmatic approach to challenging situations, you like to work in a fast pace environment within set timelines, and you are friendly and positive to work with.

- Fluent written and spoken English and excellent communication skills is a requirement.

Ideally you have:

- Extensive knowledge and experience of surface chemistry, protein conjugation, organic chemistry and analytical chemistry.

- You have experience of analytical chemistry tools; to run analyses of reagents, e.g, by HPLC and MS, to perform quality control measurements and interpret the results.

- Experience of molecular biochemistry, working with both DNA and proteins.

This is a permanent position based on the campus of Stockholm University, Stockholm, Sweden.

We offer a creative environment focused on technology and product development, a competitive compensation/salary and plenty of room of self-development as the company expands.

If above sounds like an exciting opportunity and you would like to hear more, do not hesitate and submit your application and we will get back to you!

For inquires please email us at: markus.dahl@valleyrecruitment.se Visa mindre

Manufacturing Engineer (stem-cell products), Procella Therapeutics AB

At Procella Therapeutics (part of Smartcella Holding AB) we provide advanced capabilities within stem cell therapy development and have inhouse cGMP manufacturing. We have globally licensed cardiac stem cell therapy in clinical stages (in strong collaboration with AstraZeneca) and a growing pipeline of life changing stem cell therapies. We are now seeking motivated Manufacturing Engineers, for permanent positions, to join the growing on-site manufacturing... Visa mer
At Procella Therapeutics (part of Smartcella Holding AB) we provide advanced capabilities within stem cell therapy development and have inhouse cGMP manufacturing. We have globally licensed cardiac stem cell therapy in clinical stages (in strong collaboration with AstraZeneca) and a growing pipeline of life changing stem cell therapies.

We are now seeking motivated Manufacturing Engineers, for permanent positions, to join the growing on-site manufacturing team in Tullinge, Stockholm.

Overview

You will be responsible for securing GMP compliance and technical readiness of the facility, equipment, process, and product. You will also be required to work within grade D, C, and B cleanroom classified areas applying a high standard of good manufacturing practices (GMP) and good documentation practices (GDP) as outlined by annex 1.

Your focus will be to support the GMP (clinical and/or commercial) manufacturing of ATMP, cell products and you will be required to display a continuous improvement mind set. The role includes cross-functional collaboration with other departments such as MSAT, QA, and Supply Chain.

The department will ensure compliance with Procella quality management systems, registered files, current regulatory requirements and quality criteria.

Responsibilities

- Produce clinical and/or commercial stem cells therapies in accordance with regulatory requirements.

- Support the daily activities in the GMP, cleanroom facility.

- Support cross-functional and external activities related to manufacturing.

- Execute GMP processes according to production schedules and instructions (e.g. MBR , eMBR, SOP, PTP, sampling plans, and work instructions).

- Take part in media fills / Aseptic process simulations.

- Comply with company policies, risk assessments, instructions, and protocols.

- Prepare, review, and revise GMP critical documentation.

- Participate in projects (e.g., internal, and external tech transfer activities, validations, eMBR construction, etc).

- Support periodic calibration, and maintenance and act as a superuser for equipment, instruments, and systems.

- Handling CAPA and initiation of deviation and investigations.

- Supervise and train team members in cleanroom environments and processes.

- Document and monitor quality issues through Procella quality systems.

- Initiate, review and approve change cases.

- Identifying and implementing areas of improvement.

- Ensure GMP compliance by complying with Procellas quality system and relevant guidelines, standards, and regulatory requirements

- Ensure GMP compliance within the development of documentation, revision, and training.

- Ensure GMP compliance within the validation lifecycle of equipment, systems, utilities, and processes.

Required qualifications

Practical experience:

- At least 2 years of proven experience working in a GMP manufacturing and/or quality control environment, including hands-on laboratory-based cell culturing experiences (preferably experiences growing stem-cells in various conditions).

Education:

- University degree (eg. BSc, MSc) in life science (biochemistry, chemistry, molecular biology, microbiology or in other relevant area).

This is a unique opportunity and you will be part of a great organization within the SmartCella group. Initial focus is to act hands-on to produce life changing products according to critical quality standards and to project plan. As the business grows there will be great opportunities for personal development and to take on new exciting projects/roles. You will receive a competitive compensation package including pension-, health covering- and insurance plans including a competitive monthly salary.

Submit your application today! We will review applications on an ongoing basis and hope to fill the position as soon as possible.

Reach out to Markus at markus.dahl@valleyrecruitment.se for questions regarding both the position and company.

About the company

SmartCella is a world-leading biotech & medtech company pioneering the future of targeted therapies by combining first-in-class delivery platforms with cutting-edge cell and gene therapies. The SmartCella group consist of SmartCella Holding AB, ProCella Therapeutics AB, SmartWise AB and SmartCella Solutions AB with a total of 60 employees from more than 20 nationalities.

Homepage: https://www.smartcella.com/procella/ Visa mindre

Senior Scientist – Surface Chemistry, Gnothis AB, Stockholm

Ansök    Dec 19    Valley Recruitment AB    Organisk kemist
Gnothis is hiring a Senior Scientist with strong scientific and technical skills within surface chemistry. This is a chance for you to be a part of a smart, innovative team with minimal hierarchy and maximum enthusiasm. We are seeking for a highly motivated and enthusiastic individual, ready to take on a new exciting challenge. This is a permanent position based at the campus of Stockholm University. Gnothis, founded in 2015 and supported by highly compet... Visa mer
Gnothis is hiring a Senior Scientist with strong scientific and technical skills within surface chemistry. This is a chance for you to be a part of a smart, innovative team with minimal hierarchy and maximum enthusiasm. We are seeking for a highly motivated and enthusiastic individual, ready to take on a new exciting challenge. This is a permanent position based at the campus of Stockholm University.

Gnothis, founded in 2015 and supported by highly competent and previous successful industrial professionals and technology developers, is on a mission to develop a new frontier for single molecule DNA sequencing; to break the mold on how sequencing is used as a clinical tool for the diagnosis of complex diseases.

Gnothis technology integrates a wide range of cutting-edge sciences ranging from nanotechnology, photophysics, optics, surface chemistry, biochemistry and computational science.

- You will be a part of a growing R&D team to develop protocols and methods for the chemical functionalization of Gnothis sequencing technology.

- The ideal applicant is one that aims to take on R&D responsibility for Gnothis surface chemistry, but also enjoys working with the team to solve technical challenges within a much wider range of scientific fields.

- The role will initially focus on the formation of SAMs (self-assembled monolayers) on glass and chemical functionalization of metal nanoparticles. It requires in-depth understanding and experience of how molecular interactions with surfaces are affected by reaction conditions such as the temperature, humidity, pH, ionic charges and relative concentrations of reagents.

- As a key member of Gnothis R&D team you will be involved in all stages of product development, from concept design to realized product. Responsibilities will include planning for projects, designing and executing your own experiments, and analyzing results to support project decisions and milestones.

For the right person this is an opportunity to join a focused and dedicated team with a passion for developing a new world-class technology platform!

- To fit the role, you have a Master of Science and a PhD (or comparable industrial experience) in organic chemistry, surface chemistry, material science or other relevant scientific discipline.

- As a person you are self-motivated, enjoys leading from the bench and applying your experience in chemistry.

- You lead by example, have a can-do attitude and hands-on mentality. You have a strong creative mindset to envision novel experiments, and the analytical competence to interpret and understand the molecular basis of the results.

- You have excellent analytical and problem-solving skills with a proactive approach, along with an interest in identifying, investigating, and solving technical challenges together with your colleagues.

- Fluent written and spoken English and excellent communication skills is a requirement.

- It is important that you have extensive experience of laboratory work and enjoy working in a laboratory. You ought to feel comfortable and be productive in a dynamic working environment. As an R&D team member you have a calm and pragmatic approach to challenging situations, and are friendly and positive to work with.

Ideally you are a profile with:

- Extensive knowledge of organic chemistry.

- Experience of technology development; molecular assays involving surface-protein conjugation.

- Hands-on experience of clean room facilities for nanofabrication.

- Experience of bio-chip prototyping with integrated fluidics.

- Expertise in molecular DNA technology, sequencing, oligonucleotides and DNA polymerases.

- Experience of project planning, communication, and goal setting in multi-disciplinary projects.

- Experience of product development within life science; from concept to product launch.

We offer a creative environment focused on technology and product development, a competitive compensation and plenty of room of self-development as the company expands.

If above sounds like an exciting opportunity and you would like to hear more, do not hesitate and submit your application and we will get back to you!

For inquires please email us at: markus.dahl@valleyrecruitment.se Visa mindre

Senior Valideringsingenjör med uppdrag inom farma, diagnostik och medtech.

Nu finns en kul möjlighet för dig som vill utvecklas vidare i en roll som senior valideringsingenjör! Spännande är att du kommer att ”teama” ihop med bolagets idag totalt två anställda, och som idag jobbar operativt som konsulter med både validerings- och kvalificeringsprojekt mot både globala och mindre bolag inom farma, diagnostik och medicinteknik. Detta är bara början på en hittills framgångsrik resa och där man nu sätter ambitionerna på att växa ytter... Visa mer
Nu finns en kul möjlighet för dig som vill utvecklas vidare i en roll som senior valideringsingenjör! Spännande är att du kommer att ”teama” ihop med bolagets idag totalt två anställda, och som idag jobbar operativt som konsulter med både validerings- och kvalificeringsprojekt mot både globala och mindre bolag inom farma, diagnostik och medicinteknik. Detta är bara början på en hittills framgångsrik resa och där man nu sätter ambitionerna på att växa ytterligare och svara upp mot ett ökande kundbehov i både Uppsala, Stockholm och Södertälje. Du kommer att jobba tajt med bolagets båda anställda och ha en viktig roll att fortsätta forma utvecklingen i bolaget. Detta är en unik chans för dig som vill jobba med stor frihet, med högt ansvar och med ett tajt samarbete i ett litet engagerat team. Behovet är omgående!

Du blir direktanställd i bolaget och utför sedan uppdrag som konsult, enskilt och/eller tillsammans med bolagets anställda, hos kunder i ex. Södertälje, Stockholm och Uppsala.

Vem är du?

- Du har en relevant naturvetenskaplig bakgrund inom ex. mikrobiologi, kemi, biokemi, molekylärbiologi, biomedicin, farmaci eller liknande.
- Du har solida erfarenheter, med tidigare framgångsrika aktiviteter, i att jobba i labb och/eller produktionsmiljöer enligt strikta kvalitetsdirektiv.
- Du har redan gedigna erfarenheter att jobba inom validering/kvalificering, exempelvis kopplat till rengöringsvalideringsprojekt eller inom andra områden.
- Du har en lång erfarenhet med att ha arbetat enligt satta kvalitetskrav och kvalitetsstandarder (GMP).
- Du har en vana att sammanställa och hantera ex. laborativa data, provresultat och annan omfattande komplex dokumentation.
- Du tar högt eget ansvar för din egna utveckling, tar initiativ och är gärna med att forma strategier för bolagets fortsatta väg framåt. Du trivs att jobba i en konsult- och/eller uppdragsform och där du har ambitionen att göra skillnad tillsammans med andra kollegor; att få jobba med produkter som gör skillnad för patienter och att möta samtliga kunders förväntan.

Startdatum: Så snart som möjligt, så skicka gärna din ansökan redan idag!

Om bolaget:

Idag jobbar bolagets ägare som operativ konsult inom validering/kvalificering, och som har drivit sina egna aktiviteter i över 10 år med ett väl upparbetat kundnätvärk. Bolaget, med nu totalt två anställda, erbjuder ett upplägg innefattande pension, försäkringar och en konkurrenskraftig ersättning/lön. Då kundförfrågningarna ökar så vill bolaget anställa ytterligare en medarbetare som både vill och kan driva framgångsrika konsultaktiviteter, samt vill och kan vara med att driva bolagets fortsatta utveckling och expansion.

Vid frågor ang. rollen och företaget, kontakta mig direkt på markus.dahl@valleyrecruitment.se Visa mindre

Valideringsingenjör med uppdrag inom farma, diagnostik och medicinteknik.

Beskrivning: Nu finns en kul möjlighet för dig som vill utvecklas vidare i en roll som valideringsingenjör! Spännande är att du kommer att ”teama” ihop med bolagets ägare som idag jobbar operativt som konsult med validering/kvalificering mot både globala och mindre bolag inom farma, diagnostik och medicinteknik. Detta är bara början på en hittills framgångsrik resa och där man nu sätter ambitioner på att växa och svara upp mot ett ökande kundbehov i både ... Visa mer
Beskrivning:

Nu finns en kul möjlighet för dig som vill utvecklas vidare i en roll som valideringsingenjör! Spännande är att du kommer att ”teama” ihop med bolagets ägare som idag jobbar operativt som konsult med validering/kvalificering mot både globala och mindre bolag inom farma, diagnostik och medicinteknik. Detta är bara början på en hittills framgångsrik resa och där man nu sätter ambitioner på att växa och svara upp mot ett ökande kundbehov i både Uppsala, Stockholm och Södertälje. Du kommer att jobba tajt med bolagets ägare och ha en viktig roll att fortsätta forma utvecklingen i bolaget. Detta är en unik chans för dig som vill jobba med stor frihet, högt ansvar och med ett tajt samarbete med en senior och erfaren valideringsingenjör. Behovet är omgående!

Du blir anställd i bolaget och utför sedan uppdrag som konsult enskilt och/eller tillsammans med bolagets ägare.

Vem är du?

- Du har en relevant naturvetenskaplig bakgrund inom ex. mikrobiologi, kemi, biokemi, molekylärbiologi, biomedicin, farmaci eller liknande.
- Du har god insyn i vad som innebär att jobba i labb och/eller produktionsmiljöer. Du har ett stort intresse och stor vilja att få jobba med kvalitén av produktionsprocesser kopplat till ex. läkemedels- och medicintekniska produkter.
- Kanske har du redan gedigna erfarenheter att jobba inom validering/kvalificering och kanske med exempelvis rengöringsvalideringsprojekt? Bra(!), men detta är inget krav.
- Kanske har du jobbat med aktiviteter kopplat till miljökontroller, är tekniskt lagd och kan bedöma risker kopplat till produktionsprocesser och produktionssystem? Bra(!), men detta är inget krav.
- Du har ett högt kvalitativt tänk och en god förståelse för, och en vilja, att arbeta enligt satta kvalitetskrav och kvalitetsstandarder (GMP).
- Du har en vana att sammanställa och hantera laborativ data/provresultat, och en vilja att vara med att skapa, ändra och anpassa valideringsmetoder och valideringsplaner för bolagets olika kunder.
- Du tar högt eget ansvar för din egna utveckling, tar initiativ och är gärna med att forma strategier för bolagets fortsatta väg framåt. Du trivs att jobba i en konsult- och/eller uppdragsform och där du har ambitionen att göra skillnad tillsammans med andra kollegor; att få jobba med produkter som gör skillnad för patienter och att möta samtliga kunders förväntan.


Startdatum: Så snart som möjligt, så skicka gärna din ansökan redan idag!

Om bolaget:

Idag jobbar bolagets ägare som operativ konsult inom validering/kvalificering och som har drivit sina egna aktiviteter i över 10 år. Bolaget erbjuder ett upplägg innefattande pension, försäkringar och en konkurrenskraftig ersättning/lön. Då kundförfrågningarna ökar så vill bolaget anställa ytterligare en medarbetare som vill och kan driva framgångsrika konsultaktiviteter, samt vill och kan vara med att driva bolagets fortsatta utveckling och expansion.

Vid frågor ang. rollen och företaget, kontakta mig direkt på markus.dahl@valleyrecruitment.se Visa mindre

Key Account Manager (KAM), Ferring Pharmaceutical (Stockholm/Uppsala)

About the company: Ferring Pharmaceuticals is a research-driven, specialty biopharmaceutical group active in global markets and has its own operating subsidiaries in nearly 60 countries and markets its products in 110 countries. Ferring has evolved and grown since Frederik and Eva Paulsen founded the company in Malmö, Sweden in the 1950s. The team is built on a pioneering spirit with an ambition to create life-changing treatments for people that need them... Visa mer
About the company:

Ferring Pharmaceuticals is a research-driven, specialty biopharmaceutical group active in global markets and has its own operating subsidiaries in nearly 60 countries and markets its products in 110 countries. Ferring has evolved and grown since Frederik and Eva Paulsen founded the company in Malmö, Sweden in the 1950s. The team is built on a pioneering spirit with an ambition to create life-changing treatments for people that need them. Today the headquarter is in Saint-Prex, Switzerland. Ferring employs over 6,000 people across countries and the diversity of the team brings exciting ideas and innovation. By working together, new science can be applied to unmet needs to help people improve their quality of life. Ferring is committed to supporting all employees in their career development and to ensuring all team-members receiving the right level of support and progression. Ferring has R&D centers in Brazil, China, Denmark, India, Israel, Japan, Russia, Switzerland, the UK and two in the US. The main pharmaceutical development hub is in Copenhagen. The Copenhagen and Parsippany sites drive and execute product innovation and development of new molecular entities as well as further development of the existing inline products to better meet patient needs or address new disease areas. Ferring has manufacturing sites in 13 countries. In-house production is carried out in Argentina, China, the Czech Republic, Denmark, Germany, India, Israel, Mexico, Switzerland, the UK, and the US. The Nordic commercial cluster includes Sweden, Denmark, Norway, Finland, and Iceland (representation via agent).

For further information about the company:

www.ferring.com (http://www.ferring.com)

www.ferring.se (http://www.ferring.se)

Job description:

The position as Key Account Manager within Gastroenterology and Urology is placed in the new Nordic organization, with focus primarily on Stockholm/Uppsala markets, and will report to Sales Manager for Speciality Brands (SB).

The Key Account Manager (SB) for Sweden is responsible for planning, implementing and executing activity-based sales activities in the gastroenterology and urology markets:

- The purpose of the role is both to keeping and strengthening our key products (Pentasa® and Minirin®) and keep positioning Ferring as the preferred partner among targeted HCPs.
- The purpose is also to prepare and initiate launching activities for future upcoming pharmaceutical products.
Key activities:

- Identify, build up and maintain an excellent relationship with key HCPs and hospitals
- Organize Key Doctors and Key Hospitals meetings
- Present and inform Key Doctors and Key Hospitals about the key products according to the company and market strategy
- Follow up on key accounts evolution; propose new Key Accounts, changes or removals
- Use of marketing material; product clarification regarding doubts and concerns, opposition to objections, advantages compared to competitors
- Secure good communication and collaboration across all involved functions
- Ensure that other departments complete and communicate the latest info to the KOLs if necessary
- Obtain, document and communicate internally information from the market about the doctor’s concerns on our products, or changes in the market
- Assist to the Scientific congresses and meetings determined by the company, and organize the proposals according to the budget approved
- Document activities in CRM for operational excellence and customer centricity
- Maintain strong understanding of Code of Ethics to secure activities alignment with regulations


Qualifications:

- To be successful in this role we think you have an analytical and a creative mindset, enjoy being part in a positive and fast paced changing environment where you will establish your own path including sales plans and business strategies
- Bachelor’s degree or equivalent with a background in Life Science; eg. within biology, medical or pharmacy (Lif-certification, or equivalent, is required)
- At least 3 years of sales experiences, and preferable relevant sales experiences within the gastro- and/or urology fields
- Ability and ambition to be involved in management strategy; to propose new strategies and ideas, and to translate these into successful activities
- You display a strong collaborative, adaptable and growth mindset with a clear and engaging communication style
- You are self-motivated, dedicated and goal-oriented with a high work capacity
- You have proficient computer skills


If above sounds like an exciting opportunity and you would like to hear more, do not hesitate and submit your application and we will get back to you!

For inquires please email me at: markus.dahl@valleyrecruitment.se

Valley Recruitment AB collaborates with Ferring Pharmaceuticals and supports the recruitment process of the position Key Account Manager (KAM). Visa mindre

Senior Production Engineer, Moligo Technologies AB

We are seeking for a highly motivated and ambitious person to take on the challenge as Senior Production Engineer, and as the next step as Production Manager, at Moligo Technologies. Moligo Technologies is an entrepreneurial and innovative DNA-technology company with headquarters in Solna Campus, Karolinska Institute, Stockholm. The team, of total 10 members, now plan to take the next steps in their journey to further expand and to build up the organizati... Visa mer
We are seeking for a highly motivated and ambitious person to take on the challenge as Senior Production Engineer, and as the next step as Production Manager, at Moligo Technologies.

Moligo Technologies is an entrepreneurial and innovative DNA-technology company with headquarters in Solna Campus, Karolinska Institute, Stockholm. The team, of total 10 members, now plan to take the next steps in their journey to further expand and to build up the organization by moving to new locations, setting up robust and structured R&D, production, quality and sales departments. This is an exciting opportunity to join a successful ambitious company together with highly competent team members, supported by the same entrepreneurs and investors of multiple successful biotech start-ups in Stockholm/Uppsala region.

Competences and experience:

To be successful in this role you need a solid past hands-on experience, ideally within areas such as R&D, production & quality, and within production of DNA/RNA, preferably in-vitro:

- Previous experiences working within biomanufacturing in GMP-regulated environment; eg. activities related to improvements and changes of the production, including planning, testing and validations.
- Previous experiences with large scale purification methods of DNA/RNA molecules
- Previous experiences from quality related work and process improvements; eg. activities related to establishment of manufacturing methods and batch protocols, deviation management and change requests, presentation and explanation of manufacturing process during internal inspections and audits.
- Previous role as team leader/leadership-skills


Who are you?

- To be successful in this role we think you have a university master degree and/or PhD degree in bioscience/biochemistry/molecular biology/microbiology, ideally within DNA/RNA-production & purification technology and solid phase extraction fields.
- > 2 years industrial experience from production environment with cross-functional activities together with quality control (QC) and quality assurance (QA) units.
- You need to be driven by self-motivation and with a collaborative spirit, have an analytical mindset and excellent communication skills.


We offer a creative environment with competitive compensation packages, and plenty of room of self-development as the company expands.

About the company

At Moligo Technologies, our mission is to enable the next generation of DNA based tools. From research to genome editing and diagnostics, we produce long and pure, single stranded DNA that is not limited by complexity, multifunctionality or scale.

We want to push the limit of what is possible in genome editing by providing the best tools that improve precision and reduce unexpected off-target effects. We do this by producing DNA strands that are over 10 000 bases long and over 99.99999% pure. Our enzymatic technology also allows us to produce DNA with any modifications or complexity which removed many of the limitations currently on researchers and pharmaceutical companies.

We also want to make sure that new technologies are not limited by scale. Unlike other methods, our technology allows us to produce industrial scale of DNA meaning that we can easily supply all the material for large experiments and clinical trials.

Website: https://www.moligotechnologies.com/

If above sounds like an exciting opportunity and you would like to hear more, do not hesitate and submit your application and we will get back to you!

For inquires please email me at: markus.dahl@valleyrecruitment.se

Valley Recruitment AB collaborates with Moligo Technologies AB and supports the recruitment process of the position Senior Production Engineer. Visa mindre

Konsultuppdrag Clinical Research Manager för ett innovativt diagnostikbo...

IDL Biotech (numera dotterbolag till Arocell AB) är ett diagnostikföretag som utvecklar, producerar och marknadsför In Vitro Diagnostik-tester (IVD) över hela världen för hälso- och sjukvårdssektorn. Bolagets fokus ligger inom onkologi och bakteriologi, och IDL:s produkter möjliggör sjukdomsdiagnostik; snabb och effektiv prognos och kontroll av behandlingseffektivitet mot ex. lungcancer, cancer i urinblåsa samt bakteriella sjukdomar som tyfoidfeber. Bolage... Visa mer
IDL Biotech (numera dotterbolag till Arocell AB) är ett diagnostikföretag som utvecklar, producerar och marknadsför In Vitro Diagnostik-tester (IVD) över hela världen för hälso- och sjukvårdssektorn. Bolagets fokus ligger inom onkologi och bakteriologi, och IDL:s produkter möjliggör sjukdomsdiagnostik; snabb och effektiv prognos och kontroll av behandlingseffektivitet mot ex. lungcancer, cancer i urinblåsa samt bakteriella sjukdomar som tyfoidfeber. Bolaget finns strax utanför Stockholm (Bromma), där alla företagsfunktioner, inklusive ledning, försäljning & marknadsföring, order & frakt, FoU, produktion och kvalitetssäkring finns. IDL:s produkter distribueras främst i Europa och Asien.

IDL Biotech har sedan starten 1988 satt människan först. Bolagets önskan och vision är att läkare på ett enklare sätt ska kunna upptäcka sjukdomar i tid för att på så sätt minska dödligheten inom flera svåra sjukdomsområden.

IDL har stora visioner och har som ambition att fortsätta växa och utvecklas och skapa snabbtester för fler viktiga och svåra cancersjukdomar.

Case-upplägg:

Nu söker IDL en konsult på 50% för en roll som Clinical Research Manager. Du förväntas stötta IDLs fortsatta utveckling att arbeta praktiskt ”hands-on” med att driva bolagets kliniska studier. Detta innefattar bl.a. ansvar för studieprotokoll och relaterade dokument, etiska- och biobanksansökningar, besök på studie-site, utbilda läkare/sköterskor på de kliniska siten, uppstart, monitorering och avslut av kliniska studier. Tjänsten omfattar också resor, främst inom Europa. Personen kommer också ingå i bolagets kliniska arbetsgrupp (idag 4 personer) där man tar beslut om vilka studier som skall genomföras och när.

Du blir anställd hos mitt partnerbolag som konsult (initialt på 50%), som är ett etablerat konsultbolag inom IT, Engineering & Life Science, och du utför konsultuppdraget med utgångspunkt på IDL Biotech Bromma-siten. Det finns goda utrymmen att fortsätta utvecklas under konsultuppdraget; att konsultuppdraget förlängs, går upp till 100% aktivitet (påkopplade aktiviteter inom R&D), samt potentiellt framtida utrymme för direktanställning till IDL Biotech med utökade ansvarsområden.

Vem är du och vad har du för bakgrund?

- Akademisk utbildningsbakgrund inom ett relevant område ex. medicin, farma, biomedicin eller motsvarande.
- Tidigare "hands-on" erfarenheter att driva tvärfunktionella projekt och/eller omfattande aktiviteter kopplat till kliniska studier och där du har arbetat med högt ansvarstagande, initiativtagande, driv och engagemang.


Länk till IDL-biotech: https://idlbiotech.com/

Frågor besvaras av mig på markus.dahl@valleyrecruitment.se och jag ser fram emot din ansökan så snart som möjligt då behovet är omgående. Visa mindre

Product Manager to the diagnostic company Devyser in Stockholm.

Product Manager Excited by the idea of joining a fast-growing diagnostic company where your challenge is to successfully scale a business with market-leading solutions for routine DNA diagnostics? Our vision is a world where personalized medicine is globally available thanks to simple and reliable genetic tests. With a solid track record of providing diagnostic kits within oncology, hereditary diseases and transplantation, we are now focused on growth by... Visa mer
Product Manager

Excited by the idea of joining a fast-growing diagnostic company where your challenge is to successfully scale a business with market-leading solutions for routine DNA diagnostics?

Our vision is a world where personalized medicine is globally available thanks to simple and reliable genetic tests. With a solid track record of providing diagnostic kits within oncology, hereditary diseases and transplantation, we are now focused on growth by further investing in product management, marketing and sales. We are looking for Product Managers to join us and help shape our future product portfolio to improve the lives of customers and patients.

As product manager you will be involved in product life cycle management, product marketing initiatives and customer experience activities to guide new product development. In this role, you will interface with multiple functions to contribute to building the product roadmap and execute on global product commercialization programs.

Activities and responsibilities such as;

- Guiding new product development by gathering voice of customer research, defining critical customer and product requirements, prioritizing features needed, and building associated business plan
- Conduct market and competitive analysis to define trends, strategically evaluate new market opportunities to identify products that can improve customer workflows.
- Help develop short and long-term roadmap for our current product portfolio
- Collaborate with customers and key opinion leaders to generate proof of concept data and penetrate key application areas.
- Lead product development processes as the commercial voice: building business cases, collecting customer input, writing product requirements, developing go-to-market plans, and launching products.
- Actively participate in building our customer experience program including customer interviews and net promoter system (NPS)
- Work closely with the marketing and sales teams as the product champion, conduct regional training, visit key accounts, present at trade shows, and develop initiatives to grow business.
- Develop and deliver product training programs for internal and external customers (Technical Support, Field Application Specialists, and Sales)
- Support marketing to create customer-focused product marketing content such as website copy, blog and social media posts, case studies, whitepapers, videos, newsletters and sales documentation
- Leverage data to drive decision making, prioritize new requirements and address defects/issues in the product based on business and customer impact
- Provide input to production planning based om product sales forecast to ensure proper inventory management


Experience

- Minimum 3-5+ years of experience in product management within diagnostics preferably within RNA/DNA analysis.
- Strong knowledge of the routine diagnostic market
- At least Bachelor's degree in biological sciences (genetics, molecular biology or similar.)
- Knowledge of molecular diagnostics testing domain; from sample collection and preparation to analysis
- Experience in product lifecycle management
- Familiar with the Pragmatic framework concept
- Demonstrated effective verbal and written communication skills


Personal attributes

- A strong collaborator comfortable with the hands-on operational work required to scale the business
- Able to prioritize and focus on the strategies that will move the needle
- Able to strategically reach out to both new and already established relevant contacts and manage collaborations such as establishment of external test sites.
- Is metrics-oriented
- Thrives in a fast-paced entrepreneurial environment
- Attention to details
- Experience working in a regulated environment and knowledge of IVD and LDT products
- Ability to travel up to 30% of the time
- Proficiency in English is required.
- Proficiency in languages such as Swedish, German, French, Italian or Spanish is a plus
- Excellent writing skills is a plus




About Devyser

Devyser develop, produce and commercialize genetic testing products within oncology, hereditary diseases and transplantation for use in clinical diagnostic labs. Based in Stockholm, Sweden, Devyser was founded in 2004 by three pioneers who envisioned rapid, noninvasive diagnostics based on multiplexed PCR and QF-PCR technology. This has since been applied to the front-end of sequencing workflows in order to streamline protocols. For patients, wait time and result clarity is absolutely critical. You want to be confident that you can provide accurate results quickly. Devyser simplify and streamline complex testing processes to improve your throughput, significantly reduce hands-on time and produce results you can trust. Devyser provide support and customer care through their in-house experts, who understand the day-to-day reality of the diagnostics lab. Devyser`s vision is a world where personalized medicine is globally available thanks to simple and reliable genetic tests.

Visit (https://devyser.com/)https://devyser.com/ for more information! Visa mindre

Direkt operativ CEO till det stabila Adlego Biomedical AB, Stockholm

Bakgrund Adlego firar 10 års jubileum och har genom åren byggt upp en framgångsrik verksamhet med fokus på preklinisk läkemedelsutveckling. Adlego har etablerat en gedigen kundportfölj och samarbetar med ett flertal partnerbolag för att kunna initiera, utföra och avsluta framgångsrika läkemedelskandidatstudier. Bolaget är GLP certifierade och jobbar med kvalitetssäkrade processer för att kunna leverera resultat inom områden innefattande bl.a. flertalet va... Visa mer
Bakgrund

Adlego firar 10 års jubileum och har genom åren byggt upp en framgångsrik verksamhet med fokus på preklinisk läkemedelsutveckling. Adlego har etablerat en gedigen kundportfölj och samarbetar med ett flertal partnerbolag för att kunna initiera, utföra och avsluta framgångsrika läkemedelskandidatstudier. Bolaget är GLP certifierade och jobbar med kvalitetssäkrade processer för att kunna leverera resultat inom områden innefattande bl.a. flertalet vaccin- och cancerprojekt. Bolaget är välmående och har idag fler än 70 pågående projekt med en växande årlig omsättning. Nu söker vi en person som kan komplettera arbetet tillsammans med bolagets CSO och fortsätta leda och utveckla bolaget framåt. En överlämningsperiod kommer att ske etappvis.

Ansvarsområden:

Som operativ CEO så förväntas du att leda arbetet framåt; att leda, motivera och sporra teamet, och att vara med att skapa en positiv och rolig arbetskultur och en bra arbetsmiljö i en mindre organisation. Du kommer att vara involverad i strategiskt arbete och att fortsätta arbetet med att etablera en långsiktig och framgångsrik bolag-struktur. Du kommer dessutom att utföra hands-on aktiviteter kopplat till bolagets pågående och kommande in-vivo studier samt att utföra och sammanställa kvalitativa projektrapporter enligt kundförväntan.

Kvalifikationer:

- Seniora erfarenheter med fokus på in-vivo studier, gärna med en relevant hands-on Ph.D bakgrund inom exempelvis fysiologi, farmakologi och/eller toxikologi.
- Erfarenheter av att leda personal och att skapa framgångsrika och högpresterande team.
- En tydlig och skicklig kommunikatör, och en förmåga att skapa och sammanställa rapporter för in-vivo studier kopplat till läkemedelsutveckling (innefattande exempelvis sammanställning av rådata och utförande av statistiska analyser)
- Hands- on erfarenheter och/eller solida kunskaper inom preklinisk läkemedelsutveckling är en fördel för att bli framgångsrik i rollen.


Vad erbjuder vi?

Som operativ CEO får du chansen att vara med att utveckla bolaget framåt, att leda ett högpresterande team och att vara med att skapa en långsiktig framgångsrik bolagskultur. Rollen är bred och du kommer också att vara direkt operativ innefattande olika hands-on aktiviteter. Tjänsten erbjuder en attraktiv ersättningsmodell med utrymme till delägarskap.

Om Adlego

Adlego Biomedical AB är ett privatägt företag som fokuserar på läkemedelsutveckling. Eftersom Adlego inte har specifika kopplingar med något läkemedelsföretag eller andra CRO -företag så garanteras alltid ärliga projektdiskussioner och rapporter till bolagets kunder.

Teamet arbetar i toppmoderna anläggningar som har den flexibilitet som krävs för att påbörja och avsluta både kortsiktiga grundläggande DMPK-studier, samt även krävande långsiktiga projekt på biosäkerhetsnivå 3.

Bolagets kunder drar nytta av företagets flexibla arbetssätt vilket innebär att de inte behöver betala onödiga omkostnader för kringliggande tjänster. Bolaget samarbetar med ett brett utbud av partner-företag för att kunna täcka alla delar av en preklinisk läkemedelsutvecklingsprocess.

Adlego Biomedical AB håller till i Karolinska Institutet Science Park i Solna.

Läs mer på: https://adlego.se/

Om tjänsten känns intressant, tveka inte och bifoga ditt CV via länken så tar vi dialogen vidare!

Vid frågor om tjänsten, kontakta Markus Dahl på markus.dahl@valleyrecruitment.se) Visa mindre