Quality Control Analyst (m/f/d)

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

• 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

• 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

• 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

Ihr Kontakt

Referenznummer
896264/1

Kontakt aufnehmen
Telefon:+41 44 225 50 00
E-Mail: positionen@hays.ch

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