Stellenangebot: Batch Record Reviewer (m/f/d)

Über uns

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

Aufgaben

• Investigate discrepancies such as failed process parameters or material consumption issues
• Evaluate and clarify operator comments in batch records according to GMP and ALCOA+ standards
• Collaborate with cross-functional teams to resolve batch record issues
• Provide quality impact assessments for deviations and process failures
• Use systems such as MES Syncade, DeltaV, Trackwise, SAP, LIMS, and DMS for data analysis
• Support documentation tasks including lifecycle document authoring and cleaning report compilation
• Ensure traceability and compliance in all documentation activities
• Participate in internal and external discussions related to logistics and quality
• Maintain accurate records of stock management, shipping preparation, and material receipt

Profil

• Bachelor’s degree in Life Sciences or Biotechnology (preferred but not mandatory)
• Prior experience in GMP-regulated environments is a plus
• Hands-on experience in production, logistics, and batch record review
• Familiarity with warehouse operations, including goods receipt and inventory control
• Ability to work independently and meet deadlines with minimal supervision
• Strong attention to detail and documentation accuracy
• Proficient in using enterprise systems (SAP, LIMS, MES, etc.)
• Fluent in German; English proficiency at B2 level
• Forklift experience (R1 & R2) – informal training completed
• Open to candidates without SUVA-recognized certification

Wir bieten

• Opportunity to work with Lonza, a leading company in the life sciences industry
• Gain experience in GMP and quality assurance processes
• Collaborative work environment with cross-departmental exposure

Ihr Kontakt

Referenznummer
841900/1

Kontakt aufnehmen
Telefon:+41 44 225 50 00
E-Mail: positionen@hays.ch

Anstellungsart
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