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A leading pharmaceutical company in Wuppertal is seeking an External Project Manager / Principal Scientist for CMC Analytics. You will lead analytical projects for new chemical entities, managing external partner activities and driving complex projects while ensuring regulatory compliance. The ideal candidate holds a Ph.D. in Analytical Chemistry with experience in the pharmaceutical industry. This role offers a competitive compensation package, flexible working arrangements, and various family and health benefits.
At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.
External Project Manager / Principal Scientist - CMC Analytics (all genders)
As an External Project Manager / Principal Scientist - CMC Analytics (all genders) , you will lead analytical projects for new chemical entities and manage external partner activities from pre-clinical phases to market. You will independently drive complex projects, shape innovative analytical processes, and collaborate closely with cross-functional teams. Apply your expertise in analytical chemistry and actively contribute to the continuous development of our CMC Analytics cluster.
You will lead analytical project activities for new chemical entities and support manufacturing processes at external partners, covering all stages from (pre-)clinical phases to market, while ensuring alignment with project timelines and regulatory requirements (e.g. ICH, FDA, EMA, pharmacopoeias)
You will independently manage complex projects and represent Analytical Development in cross-functional project teams
Overseeing and guiding external analytical development activities including experiment planning, data generation, and preparation of analytical reports (e.g. specifications, stability studies), as well as interpretation and presentation of results in relevant committees is also part of your role
You will prepare and review registration documents and responses to regulatory inquiries
You will be responsible for the validation of analytical methods and coordination of method transfers
You will provide analytical support for manufacturing process transfers, e.g. to internal development or production functions
You will collaborate closely with internal and external stakeholders such as Chemical Development, NBE Analytics, QA, affiliated companies, and CDMOs
You will actively contribute to the continuous development of the CMC Analytics cluster by fostering innovation and efficiency in analytical activities
You will supervise academic theses (e.g. Bachelor’s, Master’s, or PhD projects)
You will support in‑licensing activities
You hold a Ph.D. or equivalent degree in Analytical Chemistry, (Bio)chemistry, Pharmaceutical Sciences, or a related field
You have several years of proven professional experience in the pharmaceutical industry, ideally in analytical development
Experience in managing external suppliers is part of your profile
You possess deep expertise in instrumental analysis, particularly HPLC; experience in peptide analysis is a plus
You demonstrate advanced knowledge of regulatory guidelines and quality standards (e.g. ICH, GMP)
Strong leadership, communication, and project management skills are part of your profile
You think strategically, act service‑oriented, and enjoy working collaboratively in interdisciplinary teams
You have excellent written and spoken English skills; German language proficiency is an advantage
Our benefits package is flexible, appreciative, and tailored to your lifestyle, because : What matters to you, matters to us!
Be You. Be Bayer.