QA Specialist / Batch Record Review
Join a Leading Biopharma Company as a QA Specialist / Batch Record Reviewer!
Contract Type: Contract
Start Date: ASAP
Location: Visp
Workload: 100%
Duration: Until 31/03/2025
Your Mission:
â?¢ Review executed electronic and/or manufacturing protocol for compliance to GMP.
â?¢ Support implementation/revision of manufacturing protocols for GMP manufacturing.
â?¢ Ensure that internal/external GMP standards and regulatory requirements are adhered to in projects.
â?¢ Participate in cross-functional investigations to determine impact to product quality and the definition of associated corrective measures.
â?¢ Represent the Quality Unit in cross-functional teams.
â?¢ Make independent quality-related decisions based on regulatory and compliance knowledge and provide independent quality support to project teams.
â?¢ Review and approve validation documents.
Your background:
â?¢ Degree in Biology, Chemistry, Biotechnology, Life Science or other related field or experience in the field of pharmaceutical industry.
â?¢ Previous experience in GMP regulated pharmaceutical industry is an advantage.
â?¢ English fluency and German good command are an advantage.
â?¢ Ability to prioritize and manage work to critical project timelines in a fast-paced environment.
â?¢ Excellent verbal, written and interpersonal communications skills.
If this sounds like you, donâ??t hesitate to apply here or reach out directly to Veronika von Mentzer, Recruiter: Write an email.
Contract Type: Contract
Start Date: ASAP
Location: Visp
Workload: 100%
Duration: Until 31/03/2025
Your Mission:
â?¢ Review executed electronic and/or manufacturing protocol for compliance to GMP.
â?¢ Support implementation/revision of manufacturing protocols for GMP manufacturing.
â?¢ Ensure that internal/external GMP standards and regulatory requirements are adhered to in projects.
â?¢ Participate in cross-functional investigations to determine impact to product quality and the definition of associated corrective measures.
â?¢ Represent the Quality Unit in cross-functional teams.
â?¢ Make independent quality-related decisions based on regulatory and compliance knowledge and provide independent quality support to project teams.
â?¢ Review and approve validation documents.
Your background:
â?¢ Degree in Biology, Chemistry, Biotechnology, Life Science or other related field or experience in the field of pharmaceutical industry.
â?¢ Previous experience in GMP regulated pharmaceutical industry is an advantage.
â?¢ English fluency and German good command are an advantage.
â?¢ Ability to prioritize and manage work to critical project timelines in a fast-paced environment.
â?¢ Excellent verbal, written and interpersonal communications skills.
If this sounds like you, donâ??t hesitate to apply here or reach out directly to Veronika von Mentzer, Recruiter: Write an email.
À propos de l'entreprise
