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Senior Quality Assurance Specialist
GrifolsQuality Assurance Specialist in pharmaceuticals working on Quality Systems and compliance. Investigating deviations, managing customer complaints, and training personnel in a GMP environment.
Posted 6/9/2026full-timeVista • California • 🇺🇸 United StatesSenior💰 $94,000 - $130,000 per yearWebsite
About the role
Key responsibilities & impact- Work with several Quality Systems ensuring compliance with Regulatory requirements.
- Investigate and report on issues under deviation management system.
- Develop effective corrective and preventative actions.
- Interface with various departments for customer complaints resolution.
- Maintain the Quality Risk Management system and support regulatory submissions.
- Conduct investigations relating to trend analysis or problem areas.
- Train entry-level personnel.
Requirements
What you’ll need- Bachelor’s degree in Biology, Chemistry, Microbiology, Biochemistry or closely related scientific / technical discipline.
- Minimum of 5 years of experience in a pharmaceutical, GMP, or FDA regulated environment.
- Direct experience in Quality Assurance, Quality Operations, Quality Control or Quality Engineering function.
- Comprehensive knowledge and understanding of cGMPs, FDA regulations, and industry guidelines.
- Strong technical writing and organizational skills.
- Proficient in MS Office (Outlook, Word, Excel, PowerPoint).
Benefits
Comp & perks- Medical
- Dental
- Vision
- Life insurance
- PTO
- Paid holidays
- Up to 5% 401(K) match
- Tuition reimbursement
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
Quality AssuranceQuality ControlQuality EngineeringcGMPFDA regulationsDeviation managementCorrective actionsPreventative actionsTrend analysisTechnical writing
Soft Skills
Organizational skillsInterdepartmental communicationTraining