FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in cGMP compliance, quality risk management, and project management within the pharmaceutical industry, ensuring quality oversight and operational excellence across R&D projects and global initiatives.
Highest-signal resume keywords
CGMP ComplianceQuality Risk ManagementProject ManagementStakeholder ManagementCAPA Processes
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Quality SystemsRegulatory RequirementsDeviations ManagementChange ControlsValidationAnalytical DevelopmentContinuous ImprovementTraining InitiativesAuditsInspections
Soft Skills
Decision-MakingCollaboration
Industry Keywords
Pharmaceutical IndustryGMP-Relevant DocumentationQuality DeliverablesOperational ExcellenceQuality Culture
About the role
Key responsibilities & impact- Ensure quality oversight for complex R&D projects and global quality initiatives
- Act as the key QA partner for cross-functional stakeholders and project teams
- Review, approve, and release GMP-relevant documentation and quality deliverables
- Drive quality activities including risk assessments, deviations, change controls, CAPAs, and training initiatives
- Support validation, qualification, and continuous improvement projects
- Provide expert guidance on cGMP compliance and quality standards
- Contribute to audits, inspections, and due diligence activities
- Promote operational excellence and a strong quality culture across the organization
Requirements
What you’ll need- Bachelor's degree with 5+ years of experience or Master's degree with 3+ years of experience in Pharma Quality, QA, Development, or Operations
- Strong knowledge of cGMP regulations, quality systems, and regulatory requirements
- Experience in quality risk management, deviations, change controls, and CAPA processes
- Strong project management, stakeholder management, and decision-making skills
- Solid scientific, technical, and compliance knowledge within the pharmaceutical industry
- Fluent in English
- Nice to have: Experience with validation, analytical development, health authority inspections, and global project environments
Benefits
Comp & perks- Talent Management – We support your professional growth and help you develop your career.
- Work-Life Balance – Flexible working hours and the opportunity for mobile working.
- Green Mobility – Benefit from our public transportation subsidy and enjoy discounted commuting.
