Pfizer is seeking an Associate for Quality Systems who will be responsible for managing documentation related to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and Good Clinical Practices (GCP). The ideal candidate will possess a relevant degree, experience in document management, and strong communication skills to ensure compliance and effective documentation control
Job Summary
This role ensures the delivery of safe and effective products to patients through a flexible and innovative quality culture.
The incumbent is responsible for managing the issuance, retrieval, archival, and control of GMP documents and records.
Candidates must possess proficiency in document management systems and familiarity with regulatory compliance standards.
Matching Summary
Match Score: 85
Pfizer is seeking an Associate for Quality Systems who will be responsible for managing documentation related to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and Good Clinical Practices (GCP). The ideal candidate will possess a relevant degree, experience in document management, and strong communication skills to ensure compliance and effective documentation control.
Skills & Requirements
Must-have
Bachelor's Degree in Chemistry or Pharmacy
4+ years experience in Quality Systems
Proficiency in GMP, GLP, and GCP manuals
Document Management Life Cycle expertise
Experience with Electronic Document Systems
Nice-to-have
Project Planning experience
Lean or Six Sigma methodology knowledge
Strong problem-solving skills
Adaptability in dynamic environments
Experience with Generative AI tools
Key Requirements
Bachelor's Degree (Chemistry/Pharmacy) with 4+ Years Experience
Master's Degree (Chemistry/Pharmacy) with 3+ Years Experience
Proficiency in Computer Software Validation Concepts