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Quality Control Analyst
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Hays (Schweiz) AGNeuchâtel
Über diese Stelle
Quality Control Analyst #
(m/f/d)
Freelance/temporary employment for a project
Neuchatel
Start date: asap
Reference number: 896264/1
Responsibilities ###
- Perform biochemical testing and laboratory activities in accordance with approved procedures while complying with GMP/GDP requirements and Quality Control department projects
- Prepare laboratory reagents, buffers, and solutions required for testing activities / Adhere to all laboratory and company procedures
- Follow and apply all EHS (Environment, Health & Safety) requirements
- Complete laboratory forms, logbooks, and documentation in compliance with Good Documentation Practices (GDP), Good Manufacturing Practices (GMP), and ALCOA+ principles
- Escalate non-conforming and/or invalid results to the Supervisor on the same day, both verbally and/or in writing, and initiate quality events within required timelines
- Conduct laboratory investigations and support deviation management activities / Execute planned activities and proactively communicate any issues impacting deadlines or priorities
- Perform qualification protocols for reagents, consumables, and validation activities related to methods, systems, and equipment
- Ensure equipment calibration and maintenance are up to date before conducting analyses / Manage Kanban activities in real time
- Report procedural deviations and improvement opportunities to Method Owners, Equipment Owners, Supervisors, Delegates, or Subject Matter Experts
- Identify and troubleshoot routine technical issues within the scope of expertise / Prepare and/or approve laboratory solutions as required
- Maintain laboratory organization and housekeeping according to 5S standards / Support continuous improvement initiatives
Profile ###
- CFC Laboratory Technician, Biology degree, or other relevant scientific qualification
- Some years of experience in a Quality Control laboratory within a cGMP-regulated pharmaceutical environment
- Experience with laboratory investigations and GMP documentation practices
- Strong understanding of quality systems and compliance requirements
Benefits ###
- A highly motivated team and an open way of communication
- Flat hierarchies
- You will work in an international environment
- Tips on how to prepare a successful application
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