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life scientist
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lead manufacturing science and technology scientist

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  • molndal, vastra gotaland
  • posted today
last day to apply 30 december 2025

job details

last day to apply 30 december 2025

summary

  • molndal, vastra gotaland
  • ccrm nordic ab
  • permanent
  • full-time
posted 17 november 2025
    number of offers
    1
  • reference number
    JN -112025-536430
    M

    meriem echbarthi, phd

    Senior talent manager

    • +46 70 385 55 78

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randstad professional

randstad professional

we bring diverse and pre qualified professional talent and businesses together to connect the right people with the right roles. by building specialized teams, we help individuals flourish in their careers and businesses succeed.

job details

Looking for an exciting opportunity to shape the future of advanced therapies and help establish Sweden as a leader in Advanced Therapy Medicinal Products (ATMPs)? Consider applying for the Lead MSAT Scientist role at CCRM Nordic and translate breakthrough science into reliable, large-scale manufacturing processes.

...

CCRM Nordic is a non-profit organization established as a national infrastructure to accelerate the commercialization of ATMPs across Sweden and the Nordic region. CCRM Nordic actively bridge the critical gap between academic research and commercial-scale production. They provide specialized expertise, process development services, and are building a state-of-the-art GMP manufacturing facility at GoCo to help innovators translate breakthrough science into safe, scalable, and market-ready treatments. Working at CCRM Nordic means being at the forefront of a high-growth, high-impact field, directly contributing to Sweden’s national ambition to be a global leader in ATMPs and ultimately delivering life-changing therapies to patients.


What you will do:

The Lead MSAT Scientist will provide hands-on leadership and expertise in transitioning process development efforts through to a manufacturing environment. The focus will predominantly be the delivery of viral vector production platforms, aimed at improving Advanced Medicinal Therapeutic Products (ATMPs). The role will encompass the optimization, analysis, characterization, and transfer of manufacturing processes for ATMPs.


Does this sound like you? Submit your CV as soon as possible. Selection is ongoing – we won't wait until the last day! In this recruitment process, CCRM Nordic AB is collaborating with Randstad AB, where the responsible recruiter is Meriem Echbarthi, PhD (meriem.echbarthi@randstad.se), who will be happy to answer your questions.

show more

Looking for an exciting opportunity to shape the future of advanced therapies and help establish Sweden as a leader in Advanced Therapy Medicinal Products (ATMPs)? Consider applying for the Lead MSAT Scientist role at CCRM Nordic and translate breakthrough science into reliable, large-scale manufacturing processes.


CCRM Nordic is a non-profit organization established as a national infrastructure to accelerate the commercialization of ATMPs across Sweden and the Nordic region. CCRM Nordic actively bridge the critical gap between academic research and commercial-scale production. They provide specialized expertise, process development services, and are building a state-of-the-art GMP manufacturing facility at GoCo to help innovators translate breakthrough science into safe, scalable, and market-ready treatments. Working at CCRM Nordic means being at the forefront of a high-growth, high-impact field, directly contributing to Sweden’s national ambition to be a global leader in ATMPs and ultimately delivering life-changing therapies to patients.

...

What you will do:

The Lead MSAT Scientist will provide hands-on leadership and expertise in transitioning process development efforts through to a manufacturing environment. The focus will predominantly be the delivery of viral vector production platforms, aimed at improving Advanced Medicinal Therapeutic Products (ATMPs). The role will encompass the optimization, analysis, characterization, and transfer of manufacturing processes for ATMPs.


Does this sound like you? Submit your CV as soon as possible. Selection is ongoing – we won't wait until the last day! In this recruitment process, CCRM Nordic AB is collaborating with Randstad AB, where the responsible recruiter is Meriem Echbarthi, PhD (meriem.echbarthi@randstad.se), who will be happy to answer your questions.

show more
  • qualification

    • Ph.D. or equivalent in Bioengineering, Chemical Engineering, Molecular Biology, or related field. 
    • Minimum 5 years’ experience in CMC development/MSAT in biotech/pharma, ideally in cell and gene therapy. 
    • Strong understanding of process development principles, statistical analysis and QbD concepts. 
    • Essential: experience with viral vectors used in ex vivo and in vivo product modification. 
    • Essential: experience with chromatography, filtration and other separation/purification techniques for viral vector bioprocessing. 
    • Essential: experience of technology transfer to/from commercial and research organizations. 
    • Experience with analytical methods for characterization and Quality Control of ATMPs (e.g., flow cytometry, qPCR, ELISA, cell-based assays). 
    • Essential: experience in the use of QMS. 
    • Familiarity with regulatory requirements for ATMPs, including cGMP and FDA/EMA regulations. 
    • A motivation for working closely with Business Development and collaborators to plan, cost and secure projects. 
    • Excellent communication skills; proven ability to collaborate with multidisciplinary teams. 
    • Proven leadership with a track record of leading projects and mentoring team members. 
    • Highly organized, detail-oriented, and capable of managing and delivering multiple projects in a fast-paced environment. 
  • key responsibilities

    • Lead activities for the transition of processes from development into a manufacturing environment to ensure consistent product quality and process robustness. 
    • Use in-depth knowledge of viral vector biology and/or associated bioprocessing to enable delivery of robust, industrial, closed, GMP-ready processes. 
    • Lead downstream process operational activities, including establishing unit operations from viral vector harvest to final fill of Drug Substance/Product.  
    • Lead troubleshooting and resolution of technical issues in manufacturing, including root-cause analysis and implementation of corrective actions.  
    • Lead and execute process improvement projects to enhance yield, reduce variability, and improve overall performance; identify opportunities for optimization and efficiency. 
    • Collaborate with R&D teams to transfer technologies from early-stage development to manufacturing. 
    • Author and review technical documents, including protocols, SOPs, reports and regulatory submissions, to support CMC development activities. 
    • Participate in cross-functional project teams to ensure alignment of CMC development goals with overall project objectives. 
    • Stay current with advancements in ATMP technologies and contribute to continuous improvement of CMC development strategies. 
    • Mentor and provide technical guidance to team members, fostering a collaborative and innovative work environment. 
    • Maintain compliance with regulatory standards and company policies to ensure safety and quality of experimental procedures and products. 
    • Ensure compliance with regulatory standards, company policies, and safety practices


  • benefits

    Join a dedicated team of scientists and engineers working on cutting-edge therapies in a dynamic setting with significant opportunities for professional development and impact.

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working at ccrm nordic ab

ccrm nordic ab

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Förändringens Gata 10


CCRM Nordic is a newly established national infrastructure for commercialization of advanced therapy medicinal products (ATMPs). CCRM Nordic is a not-for-profit company based in GoCo Health Innovation City, Mölndal that aims to build process development and GMP ATMP manufacturing capabilities during the coming years. CCRM Nordic vision is to benefit patients by enabling commercialization of advanced therapies....
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CCRM Nordic is a newly established national infrastructure for commercialization of advanced therapy medicinal products (ATMPs). CCRM Nordic is a not-for-profit company based in GoCo Health Innovation City, Mölndal that aims to build process development and GMP ATMP manufacturing capabilities during the coming years. CCRM Nordic vision is to benefit patients by enabling commercialization of advanced therapies.