Specialist Data Integrity and CSV | Specialist Data Integrity und CSV (w/m/d)
STADA Arzneimittel AG
Job Summary
As a Specialist Data Integrity and CSV, you will be instrumental in managing and overseeing computerized systems, particularly within laboratory environments, ensuring their quality and compliance. Your daily tasks will involve providing expert advice on the validation of computerized systems, including reviewing and approving documentation, and managing overview lists. You will lead projects for the implementation or modification of these systems, develop and revise Standard Operating Procedures (SOPs), and support internal and external audits and inspections. This role requires a strong understanding of GMP topics, as you will also be responsible for conducting training sessions on CSV and Data Integrity. This position offers the opportunity to contribute to a dynamic, international team within the pharmaceutical industry, shaping the future of STADA.
Required Skills
Education
Completed degree in Natural Sciences, Engineering, Computer Science, Information Technology, or comparable qualification
Experience
- • At least five years of professional experience in the pharmaceutical industry
Languages
Additional
- High level of quality and responsibility awareness, strong organizational and negotiation skills, excellent communication skills
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