QC Associate Scientist

Vor 4 Tagen

Neuenburg, Schweiz Jobs via eFinancialCareers Vollzeit

On behalf of our client, a global leader in the pharmaceutical industry, Swisslinx is seeking a QC Associate Scientist to support critical analytical assay activities at their site in Neuchâtel. This is an exciting opportunity for a detail-oriented professional to contribute to life cycle management, validation, and daily quality control activities in a cGMP environment.

Contract Type: Contract
Start Date: ASAP
Location: Neuchâtel, Switzerland
Workload: 100%
Duration: 12 months

Your Mission:

  1. Life Cycle Management Activities:
    • Manage analytical assay activities within QC laboratories, focusing on:
    • Laboratory investigations.
    • Critical material qualification.
    • Laboratory method transfers.
    • Support daily QC activities following cGMP, company policies, and EHS requirements.
  2. Validation and Qualification:
    • Author transfer protocols and qualification plans/reports for assays and critical reagents.
    • Oversee validation and qualification activities executed by analysts, providing training and support.
    • Execute and document experiments.
  3. Investigation Leadership:
    • Investigate and troubleshoot laboratory issues to identify solutions or recommend changes.
    • Conduct and participate in risk assessments, root cause analyses, and investigations.
    • Own laboratory investigations and implement corrective and preventive actions (CAPAs).
  4. Quality Control Support:
    • Apply compliance standards and regulations to assay life cycle management activities.
    • Provide technical and statistical support for daily QC activities as needed.

Your Background:
  1. Experience:
    • University or engineering degree in analytical chemistry, biotechnology, biochemistry, or microbiology.
    • Fluent in French and English (C1 level written and spoken).
    • 1-2 years of experience in GMP pharma activities, preferably in recombinant therapeutic products.
    • Proficiency in GMP laboratory activities, method transfers, and critical reagent qualification.
    • Experience in problem-solving, deviation management, and statistical tools.
    • Proficiency with standard IT tools.
  2. Competencies:
    • Strong collaboration and teamwork mindset.
    • Excellent troubleshooting and problem-solving skills.
    • Ability to work independently in a fast-paced environment and manage multiple priorities.
    • Effective communicator with the ability to synthesize information and provide feedback.

What's on Offer:
• A 12-month contract with a leading global pharmaceutical company.
• The opportunity to play a vital role in the life cycle management of critical assays.
• A chance to expand your expertise in laboratory investigations, validation, and quality control.

If this sounds like you, don't hesitate to apply here or contact Veronika von Mentzer, Recruiter: veronika.nakev@swisslinx.com. #J-18808-Ljbffr

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