FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Manager, QA Operations
IpsenManager of QA Operations at Ipsen ensuring quality oversight of service providers involved in clinical studies. Develop quality systems to comply with standards, supporting audit readiness and continuous improvement.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in quality oversight within the pharmaceutical industry, focusing on service provider management, compliance, and continuous improvement initiatives. Proficient in maintaining quality agreements and ensuring alignment with contracts while supporting audit readiness and CAPA implementation.
Highest-signal resume keywords
Quality OversightPharmaceutical Industry ExperienceMaster’s Degree in QualityCAPA ImplementationService Provider Management
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Soft Skills
CollaborationProblem-SolvingDriving Results
Industry Keywords
Quality AgreementsAudit ReadinessContinuous ImprovementMedical AffairsR&D
About the role
Key responsibilities & impact- Oversee qualification and ongoing quality oversight of service providers
- Support Service Provider Quality Oversight Meetings and ensure follow-up on actions
- Monitor and report on service provider quality performance
- Maintain quality agreements and ensure alignment with contracts
- Support audit and inspection readiness, including CAPA implementation
- Contribute to training and continuous improvement initiatives
Requirements
What you’ll need- Demonstrated experience in the pharmaceutical industry, with a solid background in quality roles supporting medical affairs or R&D
- Experience in quality oversight of service providers within pharma
- Master’s degree or higher in a relevant scientific discipline (preferred: Master’s in quality or PhD)
- Fluent English required
- Strong skills in collaboration, problem-solving, and driving results.
Benefits
Comp & perks- Collaborative Work Environment: Work with dynamic, globally connected teams and cross-functional partners in R&D, Medical Affairs, Procurement, and Legal.
- Career Growth & Impact: Opportunities to lead or co-lead global projects, clear pathways for career progression, and the chance to make a real impact on patient safety and compliance.
- Recognition & Development: Global recognition programs, ongoing feedback, annual performance reviews, and access to learning and professional development opportunities.