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Senior QC Analyst

Senior QC Analyst

Senior QC Analyst

Senior QC Analyst

Proclinical

Pharma, Medizintechnik

Neuenburg

  • Art der Beschäftigung: Vollzeit
  • 75.000 CHF – 106.500 CHF (von XING geschätzt)
  • Vor Ort
  • Zu den Ersten gehören

Senior QC Analyst

Über diesen Job

    Salary: Highly Competitive
    1. Job type: Contract
    2. Discipline: Good Manufacturing Practice (GMP)
    3. Location: Switzerland

    Ensure the highest quality standards in pharma by leading critical lab analyses and driving continuous GMP excellence.

    Proclinical is seeking a Senior QC Analyst to support quality control activities in a pharmaceutical production environment. This role involves performing laboratory analyses and ensuring compliance with applicable procedures and standards. You will play a key role in maintaining GMP standards, troubleshooting issues, and supporting continuous improvement initiatives.

    Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

    Responsibilities:

    • Conduct laboratory analyses and approvals following cGMPs and pharmacopoeia standards.
    • Adhere to SOPs and safety protocols while performing QC activities.
    • Document results accurately in logbooks and systems, ensuring compliance with Good Documentation Practices.
    • Report non-conforming or invalid results promptly and initiate quality events as required.
    • Ensure proper calibration and maintenance of laboratory equipment.
    • Support training initiatives for analysts and act as a backup trainer for GMP education.
    • Participate in risk analyses, equipment lifecycle management, and method harmonization projects.
    • Collaborate with external partners and suppliers for technical issues and maintenance.
    • Present expertise during inspections and audits.
    • Contribute to corrective and preventive actions within the laboratory.
    • Maintain a clean and organized workspace following 5S standards.

    Key Skills and Requirements:

    • Proficiency in laboratory methods and cGMP standards.
    • Strong knowledge of data integrity principles.
    • Comfortable using standard office tools and IT systems (e.g., Microsoft Office).
    • Technical proficiency in French and English (minimum B2 level in English).
    • Ability to work collaboratively, communicate effectively, and demonstrate exemplary behavior.
    • Organized, patient-oriented, and aligned with values such as honesty, integrity, fairness, and perseverance.

    If you are having difficulty in applying or if you have any questions, please contact Olivier Worch at o.worch@proclinical.com.

    Apply Now:

    If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

    Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

    By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy

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    Unternehmens-Details

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    Proclinical

    Personaldienstleistungen

    51-200 Mitarbeitende

    Frankfurt am Main, Deutschland

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