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Teamleader Magazijn

Job in Town of Belgium, Belgium, Ozaukee County, Wisconsin, 53004, USA
Listing for: Go4Jobs
Full Time position
Listed on 2026-01-17
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
    Data Scientist
Job Description & How to Apply Below
Location: Town of Belgium

Overview

  • Support quality assurance processes for biopharmaceutical manufacturing, ensuring compliance with GMP standards and regulatory requirements.
  • Provide QA oversight across manufacturing, validation, materials, QC, engineering, and facility operations.
  • Collaborate with cross-functional teams to maintain inspection readiness and continuous improvement initiatives.
  • Review and approve documentation, including SOPs, batch records, and quality documents.
  • Ensure compliance with cGMP regulations and Good Documentation Practices.
  • Support audits and regulatory inspections, providing subject matter expertise and document retrieval.
  • Contribute to maintaining equipment calibration and maintenance compliance.
  • Assist in deviation investigations, CAPAs, and change controls within the quality management system.
Key Responsibilities & Duties
  • Review and approve incoming material documentation for GMP use.
  • Provide QA support during manufacturing operations, including area clearance and changeover activities.
  • Generate and maintain Quality-related SOPs and controlled forms.
  • Review validation documents and protocol executions for regulatory compliance.
  • Approve QC laboratory qualification documents, including equipment qualification.
  • Perform batch record review and approval to ensure compliance and accuracy.

    Support partner audits and regulatory inspections with document retrieval and expertise.
  • Collaborate with teams to drive quality excellence and continuous improvement initiatives.
Job Requirements
  • Bachelor’s degree in Biology, Chemistry, Biotechnology, or related field.
  • 2–4 years of GMP experience in Quality, Manufacturing, or QC.
  • Knowledge of cGMP regulations and Good Documentation Practices.
  • Experience with quality systems such as Veeva or SAP is advantageous.
  • Strong attention to detail and organizational skills.
  • Ability to communicate effectively across teams and departments.
  • Proficiency in reviewing and approving quality documentation and validation protocols.
  • Commitment to maintaining GMP compliance and inspection readiness.
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