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Compliance coordinator operations (all genders)

Berlin
Bayer
Coordinator
Inserat online seit: 2 Dezember
Beschreibung

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.

Compliance Coordinator Operations (all genders)

In this position, you take responsibility for the evaluation and analysis of deviations in pharmaceutical production. You will contribute to ensuring and continuously improving quality standards and support the further development of our processes with your technical expertise.


YOUR TASKS AND RESPONSIBILITIES


1. Within pharmaceutical production, you evaluate deviations and complaints based on scientific principles
2. You conduct structured root cause and failure analyses, document the results, and derive measures and concepts to prevent future errors
3. After implementation of these measures and concepts, you monitor and assess their effectiveness
4. You review, revise, and create GMP-relevant documentation (SOP, QRA)
5. You are responsible for the preparation and follow-up of regulatory inspections and customer audits
6. You prepare Ongoing Process Verification (OPV) reports
7. You coordinate and contribute to the creation of Master Batch Records (MBRs)


WHO YOU ARE


8. You hold a university degree in pharmacy or a life sciences discipline such as chemistry or biochemistry
9. You have gained initial experience in the pharmaceutical industry, preferably in production, where you acquired general knowledge of drug manufacturing processes, especially in the controlled milling and analysis of active ingredients
10. You are familiar with cGMP regulations and general quality requirements for active ingredients used in the manufacture of medicinal products for human use
11. You work independently and results-oriented
12. You bring strong teamwork, organizational skills, assertiveness, flexibility, and excellent communication abilities
13. You are capable of working under pressure and making decisions
14. Fluent German and English language skills, both written and spoken, round off your profile


This is a fixed-term position for 18 months.

WHAT WE OFFER


Our benefits package is flexible, appreciative, and tailored to your lifestyle, because: What matters to you, matters to us!

15. We ensure your financial stability through a competitive compensation package, consisting of an attractive base pay and our annual bonus. In addition, managers can recognize special contributions by granting an individual performance award or top performance award.
16. Whether it’s hybrid work models or part-time arrangements: Whenever it is possible, you will have the flexibility to work how, when and where it is best for you.
17. 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.
18. 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.
19. We promote health awareness and opportunities for selfcare through various measures, such as free health checks with the company doctor.
20. We embrace diversity by providing an inclusive work environment in which you are welcomed, supported, and encouraged to bring your whole self to work.

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