Urgent Freelance Quality Assurance Engineering Consultant (Pharmaceutical Industry)
Location: Northern Germany
Duration: Immediate Start - 12-Month Contract
Language: Must be German-speaking
We are working exclusively with a large pharmaceutical client to find a highly skilled Quality Assurance Engineering Consultant with expertise in Deviation Management, CAPA, and documentation within the pharmaceutical industry. This is a crucial role to ensure that quality systems meet regulatory requirements and maintain high standards in a highly regulated environment.
Key Responsibilities:
- Deviation Management: Manage, investigate, and resolve quality deviations, ensuring compliance with regulatory requirements.
- CAPA: Develop and monitor CAPA plans, collaborate with teams to ensure resolution, and track compliance.
- Documentation: Ensure proper documentation and adherence to all required quality standards and regulations.
- Regulatory Compliance: Ensure adherence to global standards (FDA, EMA, ICH), support audits, and track regulatory changes.
- Continuous Improvement: Drive process improvements, implement best practices, and mentor internal teams.
Qualifications and Skills:
- Proven experience in Quality Assurance (Deviation Management, CAPA, documentation).
- Strong knowledge of GSP and regulatory compliance standards.
- Excellent problem-solving, communication, and analytical skills.
How to Apply:
If you're a great fit, 📩 let's connect! DM me or share a time to chat.
