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Specialist Data Integrity / CSV Quality Schaffhausen Save Saved

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Specialist Data Integrity / CSV Quality Schaffhausen Save Saved

JOHNSON & JOHNSON

Pharma, Medizintechnik

Schaffhausen

  • Art der Anstellung: Vollzeit
  • 81.000 CHF – 113.500 CHF (von XING geschätzt)
  • Vor Ort

Specialist Data Integrity / CSV Quality Schaffhausen Save Saved

Über diesen Job

Location: Schaffhausen, Switzerland | Flexible start date

At Johnson & Johnson, health is at the heart of everything we do. Leveraging our strength in healthcare innovation, we empower a world where diseases are prevented, treated, and even cured. At Cilag AG, part of Johnson & Johnson’s Janssen Pharmaceutical division, we produce pharmaceutical products, medical devices, and active pharmaceutical ingredients (APIs) for global markets.

We are seeking a passionate Specialist, Data Integrity / CSV to champion the lifecycle management of laboratory equipment, enhance data governance practices, and contribute to lab automation. Join our Site Quality Control team in Schaffhausen and make a difference in patients' lives globally.

Key Responsibilities:

Laboratory Equipment & Software Qualification:

  • Plan and execute qualification activities (in line with GMP and regulatory standards)

  • Author qualification lifecycle documents (e.g., URS, IOPQ protocols)

  • Support the revision of procedures (WIs, SOPs) related to data integrity and equipment lifecycle management

  • Perform installation, configuration, testing, and troubleshooting on laboratory systems

Data Integrity & Governance:

  • Define requirements for new software solutions and analyze data/process flows

  • Archive or migrate legacy system data

  • Support the investigation into data integrity issues and software non-conformities (CAPA)

Cross-functional Collaboration:

  • Work with internal teams (Quality Control, R&D, IT) to ensure seamless integration of laboratory systems and data workflows.

  • Collaborate effectively with external vendors for technical support, including manufacturer qualifications, maintenance, troubleshooting, and investigations.

Qualifications:

Education:

  • M.Sc. / B.Sc. in Natural Sciences, Computer Science, Engineering, or related field
    (Alternatively: Comparable training with several years of relevant experience)

Required Skills & Experience:

  • Proven work experience in GMP-regulated environments (preferably Quality Control)

  • Strong analytical and problem-solving skills

  • Experience drafting qualification documents (clear, concise, accurate)

  • Fluent in English and basic spoken German skills (B1 or above desirable)

Preferred Skills & Technologies (advantageous but not required):

  • Hands-on familiarity with laboratory equipment qualification

  • Experience with SAP, TrackWise, or TruVault

  • Experience with virtualization (e.g., VMware, Virtual Box)

What We Offer:

  • Opportunities to shape laboratory innovation in a global company at the forefront of healthcare

  • Accessible location in beautiful Schaffhausen

  • Collaborative, inclusive work environment that values work-life balance

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