SENIOR ASSOCIATE QUALITY ASSURANCE, Breda, Noord-Brabant

The Company

Our client is a global biopharmaceutical leader committed to improving patient health. They operate in a highly regulated environment and focus on innovation, quality, and patient care. Join a company that values growth, collaboration, and a commitment to scientific excellence.

Role Description

Our client is looking for a Quality Assurance professional to provide crucial support in production. You'll ensure compliance with GMP standards, offer guidance to production teams, and be involved in quality checks and investigations. This is a great opportunity to work in a dynamic and impactful environment.

 Responsibilities

• Provide daily QA support to production staff in compliance with SOPs and work instructions.

• Act as the first point of contact for quality-related queries during production.

• Review and approve batch production records before production activities.

• Perform GMP compliance checks during commercial production runs.

• Review, compile, and prepare batch records for QP disposition.

• Initiate and manage QA deviations as necessary.

• Contribute to the development and delivery of GMP training.

• Maintain departmental performance metrics and project boards.

 Requirements

• MBO or BSc in Pharmaceutical/Life Sciences or related field (or equivalent experience).

• Minimum 3 years of experience in Quality Assurance or manufacturing within the pharmaceutical or medical device industry.

• Solid knowledge of GMP, GDP, and GCP standards.

• Strong experience in batch record review and investigations.

• Ability to work in a fast-paced environment with flexibility in shift scheduling.

• Fluent in English, both written and spoken.
  
  Other Information : Click Link To Apply 

54846