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.
QA Specialist (all genders)
We are looking for a Quality Assurance Specialist (all genders) to join our Pharmaceutical Affairs team at Bayer AG Pharmaceuticals in Berlin. In this role, you will support packaging operations for parenterals and solids, manage deviations and validations, and ensure compliance with GMP standards. Be part of a collaborative team committed to quality, innovation, and regulatory excellence.
YOUR TASKS AND RESPONSIBILITIES
- You will be responsible for overseeing the production lines in the packaging of parenterals and solids
- You will create and manage deviations, conduct root cause analyses, evaluate them, and initiate corrective actions in close collaboration with production and quality assurance (QA)
- You will assess the necessity of validation activities and lead, accompany, and coordinate these until completion
- You will develop and evaluate validation and testing plans
- You will create standard operating procedures (SOPs) related to qualification and validation
- You will be responsible for the preparation, completion, and management of change requests in pharmaceutical affairs (Change Management)
- You will evaluate and document process flows from a regulatory perspective and initiate and implement necessary compliance improvements
- You will collaborate in the development of qualification and validation master plans
WHO YOU ARE
- You have a completed university degree in pharmacy as well as a pharmacist's license
- You bring good knowledge of regulatory requirements, particularly the EU GMP Guide
- You have solid MS Office skills
- You demonstrate strong organizational abilities
- You possess assertiveness and clear verbal and written communication skills
- You show initiative and work reliably and meticulously
- You are resilient, flexible, and enjoy working in a team
- You have excellent German language skills and good English language skills
WHAT WE OFFER
Our benefits package is flexible, appreciative, and tailored to your lifestyle, because: What matters to you, matters to us!
- We ensure your financial stability with a competitive salary between 77.300€ and 93.800€ per year (full-time) plus a variable component. Your compensation is based on your qualifications, skills, and professional experience.
- Your family is a top priority. We offer loving company daycare centers at multiple locations, support in finding childcare, time off for the care of elderly or dependent family members, summer camps for children, and much more.
- We support your professional growth by providing access to learning and development opportunities, training programs through the Bayer Learning Academy, development dialogues, as well as coaching and mentoring programs.
- We promote health awareness and opportunities for selfcare through various measures, such as free health checks with the company doctor.
- We embrace diversity by providing an inclusive work environment in which you are welcomed, supported, and encouraged to bring your whole self to work.
This position is limited to 12 months.
Be You. Be Bayer.
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Location:
Germany : Berlin : Berlin
Division:
Pharmaceuticals
Reference Code:
871467
Job Segment:
QA, Quality Assurance, Pharmaceutical, Compliance, Law, Quality, Technology, Science, Legal