Senior Compliance Specialist | Senior Compliance Specialist (m/w/d)
Randstad Professional
Job Summary
As a Senior Compliance Specialist in the pharmaceutical industry, you will play a pivotal role in managing GMP processes related to the qualification of disposables and packaging materials. Your day-to-day responsibilities include overseeing complex Change Control processes and lifecycle management, ensuring the timely implementation of cross-departmental change requests. You will be responsible for drafting and revising GMP documentation, including specifications and SOPs, while collaborating closely with supply chain, quality assurance, and production teams. Additionally, you will handle deviations, investigations, and CAPAs, and support the preparation for audits and inspections. This role is ideal for a professional with a strong background in pharmaceutical quality control who thrives in a collaborative, cross-functional environment. You will be instrumental in maintaining regulatory compliance while driving quality excellence across the organization. The position offers long-term security, comprehensive social benefits, and the opportunity to work with a leading partner in the pharmaceutical sector.
Required Skills
Education
Completed Diploma or Master's degree in Pharmacy, Chemistry, Biotechnology, or a comparable field.
Experience
- Professional experience in pharmaceutical quality control
- Several years of professional experience in GMP-related roles
- Experience with regulatory requirements for disposables and packaging materials
- Proven track record in managing cross-departmental quality processes and investigations
Languages
Additional
- Must be able to work in Biberach, Germany. Valid work permit for Germany required.
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