About Sanofi:
We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.
About the job
MSAT (Manufacturing, Science, Analytics and Technology) Vial & Cartridge Filling Excellence Frankfurt mission is to ensure successful maintenance and transfer-in of innovative drug products (monoclonal antibodies = mAB, microbial proteins) to FBC BLU (Frankfurt BioCampus, Biologics Launch Unit), and life cycle management (LCM) activities of marketed insulins products for FBC.
Our Galenics team, which is part of MSAT, is supporting the products transfer and LCM activities by process development studies and by the implementation and maintenance of Single Use Systems.
As Single Use Systems expert, you will be part of the Galenics team. You will be responsible for the evaluation (Extractables & Leachables, Filter Validation) of single use technology (e.g. filters, tubings, bags, assemblies) and development/establishment of new disposables used for the production of injectable drug products (mAB, microbial proteins and insulins) at FBC.
Main responsibilities:
Extractables & Leachables (E&L) and Filter validation assessment
Collect the necessary technical information
Compile the available technical information and perform the assessment
Coordinate the review and approval according to project timelines
Plan, coordinate and perform Leachables and Filter Validation studies with external companies
Work in close cooperation with the product team according to the project needs
Act as primary process owner for filter validation and E&L incl. presentation of relevant topics during audits and share expertise at global level (e.g. in a “Community of Practice”)
Support regulatory dossier preparation and answers to Health Authority questions
Support Change Control and Deviation process
Support trouble shooting activities concerning Single Use Technology
Creation of GMP documents (e.g. SOPs, PQ Plan)
Apply and optimize Environmental Sustainability by Design principles into development of new products.
About you
Education and Professional experience
Master in science (e.g. Pharmacy, Chemistry, Biotechnology)
Professional experience in the pharmaceutical industry preferably in Quality Assurance or in Drug Product manufacturing
Technical skills & Competencies / Languages
Precise way of working even under time pressure,
Good organization skills,
Very good knowledge in German and English (in writing & verbally), additional languages advantageous
Profound MS-Office knowledge
Ability to work in a regulated, international environment in diverse teams
Good communication and presentation skills
Why choose us?
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!