QA Auditor - CAPEX Projects
On behalf of our client, a leading international biotechnology company based in Visp, Swisslinx is looking for a QA Auditor. If this is you, you will be responsible for Capital Expenditures (CAPEX) projects, and be pivotal in ensuring that new facilities are built and operated in compliance with stringent GMP requirements, safeguarding product quality and regulatory adherence.
Contract type: Contract
Start Date: 1st June 2024
Location: Visp
Workload: 100%
Work type: Hybrid
Duration: 7 months (possibility of extension)
Your mission
1. Lead and Co-Auditor:
â?¢ Plan and conduct detailed internal audits for ongoing CAPEX projects to ensure compliance with GMP.
â?¢ Document and report findings, managing follow-up actions to address non-compliance issues.
2. Commissioning & Qualification (C&Q):
â?¢ Review and monitor C&Q plans to verify they meet all required GMP standards.
â?¢ Ensure thorough execution of C&Q activities, confirming alignment with approved protocols.
3. Compliance with GDocP and Data Integrity:
â?¢ Verify the integrity and completeness of the General Document of Certified Product.
â?¢ Oversee data management practices to ensure all data complies with GMP and Data Integrity standards.
Your goals
â?¢ Guarantee Compliance: Ensure all elements of CAPEX projects comply with GMP standards, focusing on design integrity and operational effectiveness.
â?¢ Maintain Regulatory Standards: Lead efforts to keep projects aligned with industry regulations and internal quality benchmarks.
Your background
â?¢ 3+ years of professional experience in quality assurance, able to start the project with minimal training.
â?¢ English language at professional fluency (mandatory).
â?¢ Experience working in GMP environments.
What's on offer
â?¢ A 7 month contract, with possibility of extension.
â?¢ a great opportunity to develop your career at a leading international biotechnology company.
If this sounds like you, apply down below or reach out directly to Hugo Palejowski, recruiter: Write an email.
Contract type: Contract
Start Date: 1st June 2024
Location: Visp
Workload: 100%
Work type: Hybrid
Duration: 7 months (possibility of extension)
Your mission
1. Lead and Co-Auditor:
â?¢ Plan and conduct detailed internal audits for ongoing CAPEX projects to ensure compliance with GMP.
â?¢ Document and report findings, managing follow-up actions to address non-compliance issues.
2. Commissioning & Qualification (C&Q):
â?¢ Review and monitor C&Q plans to verify they meet all required GMP standards.
â?¢ Ensure thorough execution of C&Q activities, confirming alignment with approved protocols.
3. Compliance with GDocP and Data Integrity:
â?¢ Verify the integrity and completeness of the General Document of Certified Product.
â?¢ Oversee data management practices to ensure all data complies with GMP and Data Integrity standards.
Your goals
â?¢ Guarantee Compliance: Ensure all elements of CAPEX projects comply with GMP standards, focusing on design integrity and operational effectiveness.
â?¢ Maintain Regulatory Standards: Lead efforts to keep projects aligned with industry regulations and internal quality benchmarks.
Your background
â?¢ 3+ years of professional experience in quality assurance, able to start the project with minimal training.
â?¢ English language at professional fluency (mandatory).
â?¢ Experience working in GMP environments.
What's on offer
â?¢ A 7 month contract, with possibility of extension.
â?¢ a great opportunity to develop your career at a leading international biotechnology company.
If this sounds like you, apply down below or reach out directly to Hugo Palejowski, recruiter: Write an email.
Über die Firma
