Glycothera is a specialized CDMO supporting biologics development across cell line development, process development, analytics, and GMP-aligned testing. Operating from integrated sites in Julich and Hanover, Germany, the company works within a unified scientific and quality framework that enables reliable, regulatory-ready CMC execution. With nearly three decades of development experience and long-standing contributions to biologics supported by EMA and FDA approvals, Glycothera partners with biotech and pharmaceutical companies to advance development programs with scientific depth, precision, and consistency.
We are currently looking for a manager to strengthen our R&D capacity at our Jülich site. The role focuses on the generation of regulatory-compliant CHO-K1 cell lines for the production of biopharmaceuticals.
Manager Cell Line Development (m/f/d)
We are a growth-oriented biopharmaceutical company focused on the development and manufacture of biologic drugs. To strengthen our Cell Line Development team, we are looking for a committed leader, effective immediately, to actively help shape our processes and provide technical and strategic leadership for our team.
Your Responsibilities
Technical and functional leadership of a Cell Line Development (CLD) team, including resource planning, staff development, and performance reviews
Planning, coordination, and management of commercial CLD projects, from cloning through GMP-compliant cell banking
Responsibility for cell line development of recombinant proteins (e.g., monoclonal antibodies and fusion proteins) in CHO and other expression systems
Monitoring and optimization of the internal CLD workflow, in particular the fed-batch process in miniaturized bioreactor systems (ambr15, ambr250) and shake flasks
Experience in the establishment of cell banks (MCB, WCB) in accordance with GMP requirements, including cell bank documentation and qualification, is desirable
Preparation, review, and approval of regulatory documents such as SOPs, qualification plans, and CLD CMC sections for regulatory submissions
Analysis, interpretation, and presentation of analytical data from cell culture, fed-batch processes, and quality analytics - both internally and to customers and authorities
Ensuring data integrity, traceability, and a high standard of scientific documentation quality
Close collaboration with Process Development, Quality Assurance, Regulatory Affairs, and Project Management
Continuous development of methods, workflows, and standards within CLD, including evaluation of new technologies and automation solutions
Your Profile
Required Qualifications
Scientific university degree (Master's / Diploma / PhD) in Biotechnology, Biology, Biochemistry, or a related field
>3 years of professional experience in CLD, with in-depth practical knowledge of cloning, pool selection, characterization, and scale-up of mammalian cell lines (in particular CHO cells)
Experience leading commercial development projects, including timeline, budget, and stakeholder management
Demonstrable leadership experience managing scientific teams, with a proven ability to motivate, develop, and guide team members toward shared goals.
Proven experience in preparing GMP-compliant documentation, including SOPs, qualification documents, and CMC submissions
Strong analytical skills with experience evaluating, interpreting, and presenting complex data sets from cell culture and protein analytics.
Excellent communication skills in both German and English (written and spoken), enabling effective collaboration across diverse teams and stakeholders.
Preferred Qualifications
Experience in process development with miniaturized bioreactor systems, in particular ambr15 and ambr250, as well as shake flask systems
Knowledge of cell banking (generation, qualification, and storage of MCB/WCB) in accordance with ICH and GMP guidelines
Industry background from a CDMO, pharmaceutical company, or comparable commercial environment
Knowledge of the application and development of analytical methods (in particular: qPCR, dPCR, Southern blot, N-glycan analysis (RFMS), HP-SEC, CEX, cIEF, CE-SDS, binding assays, etc.) for cell line and protein characterization
Personal Competencies
Strong sense of responsibility and an independent, structured way of working
Excellent teamwork and communication skills - at both the staff and management level
Proactive, solution-oriented working style with strong analytical thinking
Quick comprehension and the ability to set priorities in a dynamic environment
High level of self-motivation, commitment, and a hands-on mentality
Very good analytical thinking and confident scientific decision-making
Accurate, quality-conscious working style with an eye for detail
Enjoyment of developing team members professionally and fostering a constructive team culture
What We Offer
A responsible leadership role in an innovative biopharmaceutical company
The opportunity to actively help shape modern cell line development technologies
Flat hierarchies, short decision-making paths, and a collegial working environment
Individual training and development opportunities
Room for professional and personal growth, and the chance to actively shape processes, structures, and team capabilities
Attractive, performance-based compensation and modern laboratory equipment
Flexible working hours and the option of remote working by arrangement
Your Application
We look forward to receiving your complete application (cover letter, CV, relevant references), including your earliest possible start date. Please submit your documents through the apply button.
We welcome applications from all individuals, regardless of gender, age, background, or disability.
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Glycothera Pharmaceutical Services is a leading global service provider for contract development and analytics for biotherapeutics at all stages of product life cycle. With our expertise in the development of biologics (recombinant proteins such as monoclonal antibodies, cytokines and hormones), manufacturing sciences, analytics, quality control and regulatory strategy we support a broad range of...
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