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Quality Control Analyst

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ZeitarbeitErfahrung nicht angegebenVor OrtNeuchâtel

Standort

Neuchâtel

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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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