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QC Analyst

QC Analyst

QC Analyst

QC Analyst

Proclinical

Pharma, Medizintechnik

Neuenburg

  • Art der Anstellung: Vollzeit
  • 73.000 CHF – 100.500 CHF (von XING geschätzt)
  • Hybrid
  • Zu den Ersten gehören

QC Analyst

Über diesen Job

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

    Proclinical is seeking a QC Analyst to support quality control activities in a pharmaceutical laboratory setting. This role involves performing analyses and sampling within a GMP-compliant environment, contributing to the establishment of a new production facility. You will play a key role in ensuring compliance with procedures, safety guidelines, and quality standards while 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 applicable procedures, cGMPs, and pharmacopoeias.
    • Adhere to SOPs and maintain accurate documentation in line with Good Manufacturing Practices (GMP).
    • Report non-conformities or invalid results promptly and initiate quality events as required.
    • Ensure compliance with EHS (Environmental, Health, and Safety) regulations and actively promote adherence among colleagues.
    • Execute qualification protocols for reagents, consumables, methods, systems, and equipment.
    • Perform data entry, result supervision, and reconciliation of controlled documents.
    • Support equipment maintenance, calibration, and troubleshooting activities.
    • Participate in continuous improvement initiatives, risk analyses, and periodic system reviews.
    • Train team members on equipment and GMP practices, acting as a backup trainer when needed.
    • Collaborate with external partners, suppliers, and internal departments to ensure quality standards are met.
    • Present expertise during inspections or audits and contribute to regulatory submissions.

    Key Skills and Requirements:

    • Background in microbiology or equivalent experience in the pharmaceutical or biotechnology industry.
    • Familiarity with laboratory methods, cGMP standards, and data integrity principles.
    • Proficiency in standard office software (e.g., Microsoft Office) and technical English (B2 level minimum).
    • Strong organizational skills, teamwork orientation, and effective communication abilities.
    • Commitment to upholding company values such as honesty, integrity, fairness, and perseverance.
    • Fluency in French and technical English is essential.

    If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@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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    Proclinical

    Personaldienstleistungen

    51-200 Mitarbeitende

    Frankfurt am Main, Deutschland

    Bewertung von Mitarbeitenden

    Gesamtbewertung

    Basierend auf 7 Bewertungen

    Vorteile für Mitarbeitende

    Flexible Arbeitszeiten
    Home-Office
    Kantine
    Barrierefreiheit
    Gesundheitsmaßnahmen
    Training
    Günstige Anbindung
    Vorteile für Mitarbeitende
    Veranstaltungen
    Privat das Internet nutzen
    Hunde willkommen

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