Overview
Commissioning and Qualifying Laboratory Consultant Jobs in Bern, Switzerland at Consultys Suisse
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Key Responsibilities
Plan and execute qualification activities (IQ/OQ/PQ) for laboratory equipment such as HPLC, GC, balances, and incubators.
Draft and review protocols, reports, and procedures related to equipment qualification.
Monitor preventive maintenance, calibrations, and periodic verifications to ensure compliance.
Collaborate with the QC team to ensure analytical results comply with quality standards.
Investigate deviations and propose corrective and preventive actions (CAPA).Ensure all qualification activities align with GMP guidelines and international regulations (ICH, FDA, ISO).Maintain accurate and
up-to-date
technical and quality documentation.
Train laboratory staff on proper equipment use and qualification standards.
Work closely with suppliers to troubleshoot technical issues.
Contribute to laboratory
process optimization
and improvement projects.
Stay updated on new technologies and equipment to enhance laboratory performance.
Required Profile Master’s degree (or higher) in Analytical Chemistry, Biotechnology, Pharmacy, or a related field.
At least 3 years of experience in a similar role, preferably in a GMP environment.
Proficiency with laboratory instruments (HPLC, GC, spectroscopy, etc.).Strong knowledge of GMP regulations and international standards (ICH Q7/Q9, FDA).Experience in drafting and reviewing technical documents.
Fluent in English and German (both written and spoken).Strong organizational skills with the ability to manage multiple projects simultaneously.
Excellent
communication
and
teamwork
abilities.
Seniority Level: Entry level
Employment Type:
Full-time
Job Function:
Manufacturing and
Quality Assurance
Industries:
Business Consulting and Services and Pharmaceutical Manufacturing
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Title: Commissioning and Qualifying Laboratory Consultant
Company: Consultys Suisse
Location: Bern, Switzerland
Category: Healthcare, Quality Assurance – QA/QC
