Latest Career Opportunity at MSD Senior Specialist Quality Assurance for Large Molecule Manufacturing- Apply Now
MSD, a global leader in pharmaceutical innovation, is hiring a Senior Specialist Quality Assurance for its Large Molecule Manufacturing Plant. This role offers an opportunity to ensure regulatory compliance, oversee quality assurance activities, and collaborate with key teams. Open to candidates across Europe, the Middle East, Africa, Latin America, and Asia Pacific, this position is ideal for experienced biopharmaceutical professionals. Apply now and be part of MSD’s mission to improve global health.
Senior Specialist Quality Assurance for Large Molecule Manufacturing Plant
Job Description: The following job opportunity is open for residents of Europe, Middle East, Africa, Latin America & Asia Pacific regions.
Job Summary
Quality Assurance for Large Molecule Manufacturing plant (Drug Product)
Key Responsibilities:
- Quality Oversight: Report to the Quality lead and provide general direction on quality goals and objectives.
- Regulatory Compliance: Ensure quality assurance activities comply with regulatory requirements.
- Manufacturing Support: Provide ongoing quality support to External Partners.
- Collaboration: Work collaboratively with relevant teams to address quality-related matters.
- Validation Strategies: Support validation strategies for new and existing products.
- Technical Review: Conduct technical reviews of process changes and deviations.
- Issue Resolution: Troubleshoot quality-related manufacturing issues.
- Efficiency Improvement: Develop more efficient methods to meet regulatory requirements.
Education and Experience Requirements for MSD Senior Specialist Quality Assurance
Education: Bachelor’s or master’s degree in related fields.
Experience:
- Minimum 15 years of experience in quality assurance within biopharmaceutical operations.
- Proven experience in highly regulated manufacturing environments.
- Strong knowledge of quality systems and regulatory compliance in the biopharmaceutical industry.
- Familiarity with change management processes and process validations.
- Proficiency in large molecule manufacturing, in process controls, and batch records review.
Preferred Experience and Skills:
Preferred Skills: Familiarity with organizational tools and digital manufacturing processes.
Employee Status: Regular
Relocation: Flexible
VISA Sponsorship: Available
Travel Requirements: Hybrid
Job Posting End Date: 04/25/2025
