Jobs für gmp operation apprentice bei Luzern

Michael Page Switzerland recherche un spécialiste des opérations QA engagé pour soutenir l'équipe qualité dans l'assurance GMP et la libération des documents qualité. Vous contribuerez à la conformité réglementaire, collaborerez avec les départements production, qualité et chaîne d'approvisionnement, et participerez au développement et à la...

LHH is seeking an Associate Specialist Downstream Operations (m/w/d) for a leading biotechnology client in the greater Lucerne area to join their Schachen manufacturing team on site.In this hands-on role, you will contribute to GMP manufacturing of innovative early-phase biologics, supporting downstream processing while upholding quality, compliance, and...

Randstad Switzerland is seeking a Quality Assurance Operations Specialist in Luzern, Switzerland. The role involves supporting GMP material release/release decisions, reviewing GMP records, and ensuring adherence to cGMP standards at the Schachen Site.End Date: 31.08.2028; Home office up to 2 days per week; standard working hours. The ideal candidate holds a...

Renommiertes PharmaunternehmenStart sofort // 2 Jahres Vertrag // Hybrid in Schachen (60=vor Ort/40=Remote)FirmenprofilRenommiertes PharmaunternehmenStellenbeschreibungPrüfung und Bewertung von GMP-relevanten Dokumenten, Aufzeichnungen und QualitätssystemenUnterstützung bei der Freigabe oder Sperrung von GMP-Materialien und KomponentenMitarbeit bei...

Michael Page International (Switzerland) SA sucht eine Fachkraft im GMP-Umfeld zur Prüfung von GMP-Dokumentationen und zur Unterstützung bei der Freigabe von Materialien. Sie arbeiten eng mit Produktion, Qualität und Supply Chain zusammen, um Compliance und Datenintegrität sicherzustellen.Sie verfügen über ein relevantes Studium, verhandlungssichere...

MSD Schachen site is seeking a Quality Operations Specialist to support GMP compliance, quality initiatives, quality systems, and SOP management within the Global Development Quality Operations team at the Schachen site.The role involves assisting with material release and rejection activities, reviewing GMP documentation, and ensuring adherence to GMP...

Renommiertes Pharmaunternehmen Start sofort // 2 Jahres Vertrag // Hybrid in Schachen (60=vor Ort/40=Remote) About Our Client Renommiertes Pharmaunternehmen Job Description Prüfung und Bewertung von GMP-relevanten Dokumenten, Aufzeichnungen und Qualitätssystemen Unterstützung bei der Freigabe oder Sperrung von GMP-Materialien und Komponenten Mitarbeit...

K-Recruiting Life Sciences is seeking a Specialist GDQ QOS – GMP Quality Operations to support the Global Development Quality Operations team and ensure GMP compliance across development activities.Responsibilities include reviewing GMP documentation, participating in batch release activities, and contributing to SOP management and cross-functional quality...

Michael Page sucht im Auftrag eines renommierten Pharmaunternehmens eine qualitätsorientierte Fachkraft für GMP-Dokumentationsprüfung. Sie prüfen GMP-relevante Unterlagen, unterstützen Freigaben, arbeiten an Compliance-Initiativen und verbessern Qualitätsprozesse.Voraussetzung ist ein naturwissenschaftliches Studium (Bachelor oder höher) und...

Renommiertes Pharmaunternehmen sucht einen QA Operations Specialist, der das Quality-Team bei GMP-Compliance unterstützt und qualitätsrelevante Dokumentationen freigibt oder sperrt. Sie arbeiten eng mit Produktion, Qualität und Supply Chain zusammen, um eine hohe Datenintegrität zu gewährleisten.Sie verfügen über ein abgeschlossenes Studium in einem...

Merck & Co., Inc., Rahway, NJ, USA, seeks a Compliance Excellence Lead (P3) at Schachen to drive GMP compliance and quality systems in biologics manufacturing. You will enable end-to-end issue resolution, risk-based decision-making, and ongoing inspection readiness in collaboration with Manufacturing, Quality, Engineering, and MSAT.You will lead deviation...

Our Company in Lucerne, Switzerland, seeks a Packaging Operations Specialist to support general packaging activities, investigations, and SAP quality notifications within GMP-controlled areas. You will review batch records, update SOPs, and assist training and archiving tasks to ensure compliance.The role requires aBachelor or Master’s degree with relevant...

The Global Development Quality Operations (GDQ QOS) team supports GMP compliance, quality initiatives, quality systems, SOP management, and cross-functional projects at the MSD Schachen site.Project title: Quality Operations Specialist m/w/dType of employment: PayrollSkills: Quality Operations,GMPProject start: 01.09.2026Key ResponsibilitiesSupport GMP...

Specialist GDQ QOS – GMP Quality Operations (M/W/D) Responsibilities: Support the Global Development Quality Operations (GDQ OPS) team in ensuring GMP compliance and quality standards. Perform GMP documentation, system, and quality record reviews in support of Quality Operations activities. Support the release or rejection of GMP materials and components...

Randstad Switzerland is recruiting a Production Operator for an international pharmaceutical company based in canton Lucerne. The role supports Biologics Manufacturing Science and Operations and drug substance bioprocess activities.The position is a 1-year temporary contract via Randstad with 100% onsite work, requiring at least 1 year in pharma/biotech and...

Aristo Group in Lucerne, Switzerland, invites applications for a Process Engineer (m/f/d) in Upstream Operations. The role requires full onsite presence to integrate with an established team and support GMP manufacturing of early-phase clinical therapies.The position emphasizes setting up and troubleshooting upstream processes, adherence to GMP and EHS...

For one of our clients, a leading biotechnology company in the greater Lucerne area, we are currently seeking an Associate Specialist Downstream Operations (m/w/d) to join their manufacturing team in Schachen. In this hands‑on role, you will contribute to the GMP manufacturing of innovative early‑phase clinical therapies, playing a key part in the...

CK QLS is seeking an Associate Specialist in Downstream Operations for a 12-month, full-time on-site role in the greater Lucerne area. The position focuses on supporting GMP manufacturing of early-stage therapies, with responsibilities spanning setup, execution, and documentation of downstream processes.The candidate should have 1–2 years of pharma/biotech...

Produktionsoperator GMP Biotech (m/w/d)Deine Chance im Herz der biotechnologischen Fertigung – werde Teil eines globalen Life-Sciences-Teams!Eintritt: Ab sofort | Einsatzort: Schachen (LU) | Home-Office: Nicht möglich (Präsenz erforderlich)Über unseren KundenFür unseren Kunden, ein international führendes Unternehmen im Bereich der biopharmazeutischen...

Merck at the Schachen site in Switzerland seeks a Compliance Excellence Lead (P3) to drive GMP deviation resolution, CAPA definitions, and robust quality systems. You will lead investigations, support changes, and enable timely, compliant manufacturing tasks.With autonomy and project leadership, you will partner with Manufacturing, Quality, Engineering and...