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About the role
Key responsibilities & impact- Oversee the complaint handling process to align with company policies and GMP/GDP regulations.
- Handling product quality issues incl. temperature excursions, deviations and follow up on actions to resolve compliance issues
- Contribute to moderately complex projects by managing your time effectively and planning short-term work activities.
- Engage with stakeholders to address product quality related issues
- Support GMP/GDP audits and inspections
- Assist with audit Corrective & Preventive Actions (CAPAs), review documentation related to repackaging and relabeling
- Compile Key Performance Indicator figures
- Support the local release of incoming finished products is performed in compliance with GDP regulations and Pfizer procedures prior to the distribution for sale in the respective market (e.g. Bulgaria, Bosnia, Croatia or other)
Requirements
What you’ll need- University degree in Life science( Pharmacy, Biology, etc.)
- Solid understanding of regulatory GDP/GMP compliance issues related to the manufacturing and distribution of medicinal products
- Excellent organizational skills and the ability to juggle multiple priorities
- Strong collaboration, communication, and interpersonal skills to work effectively with local, regional, and global colleagues
- Proficiency in using System Application and Products, and Microsoft Office Suite
- Technical expertise to handle complex quality assurance and control tasks
- Fluency(written and verbal) in English and local language
Benefits
Comp & perks- Hybrid work assignment
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
Regulatory ComplianceQuality ControlKey Performance Indicator CompilationTechnical Expertise in Quality AssuranceProduct Quality Issue Resolution
Soft Skills
Organizational SkillsCollaborationCommunicationInterpersonal SkillsTime Management
