Job Description
Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
The QA Specialist plays a critical role in ensuring that all biotechnology and pharmaceutical products meet regulatory standards and internal quality specifications. This role involves monitoring, auditing, and maintaining quality control processes throughout the product lifecycle, from research and development to production, testing, and distribution. The QA Specialist works to identify, investigate, and resolve quality issues, ensuring compliance with Good Manufacturing Practices (GMP), FDA regulations, and other applicable guidelines.
Key Responsibilities:
Quality Oversight:
Documentation and Record Keeping:
Auditing and Inspections:
Quality Control:
Validation and/or Product Release:
Risk Management:
Training and Development:
Qualifications:
Preferred Qualifications:
Key Competencies:
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