Specialist Data Integrity / CSV Quality Schaffhausen Save Saved
Specialist Data Integrity / CSV Quality Schaffhausen Save Saved
Specialist Data Integrity / CSV Quality Schaffhausen Save Saved
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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