Global GMP Auditor

Sandoz

Poland

Job responsibilities:

  • Plan, lead, conduct, document, report, and follow-up of GMP audits according to the requirements specified in the respective Novartis/ Sandoz procedures as well as applicable regulations, standards, quality agreements, and guidance documents.
  • Audits will be focused to mid-low risk manufacturing and other GMP activities, on the basis of actual experience/expertise
  • Provide technical guidance and training on audit activities.
  • Ensure appropriate escalation to responsible management in case of critical findings and support immediate follow-up measures according to Novartis/ Sandoz requirements on Management Escalations and other relevant procedures. Ensure adequate definition and recording of mitigation plans when applicable.
  • Assess the adequacy of responses (CAPA plans) to audit findings in cooperation with the stakeholder QA representative and Auditee.
  • Maintain current knowledge of regulations, standards, and guidance documents.

Job requirements:

Education (minimum/desirable):

  • Degree in Chemistry, Pharmacy, Biology, Engineering or another related science
  • Other degrees with relevant experience may be accepted

Languages:

  • Excellent oral and written English communication skills. Preferable: Good knowledge/mother tongue of an additional language (e.g. German, French, Italian, Chinese, or Spanish) is preferred

Experience:

  • At least 10 years broad experience in Pharmaceutical or Medical Device Industry.
  • The operational experience should include QA/QC management and manufacturing, or development or other relevant experience e.g. working at a regulatory health authority.
  • 3 years auditing experience preferred, and excellent knowledge of regulatory
  • requirements. Willingness to travel approx. 60% of the time.
  • Expertise in at latest, one of the following areas: DP Manufacturing, Laboratories activities, Medical Devices, API, Excipients, Sterile, Biologics, Microbiology, Computer System Validation, Packaging activities, Quality Systems.
  • Experience and/or interaction with local Health Authority and sporadically with other Health Authorities.
  • Strong interpersonal skills, including diplomacy and persuasion, used in obtaining cooperation and consensus with Sandoz colleagues, vendors and customers.
  • Sound and practical judgement in the interpretation and application of regulations and standards

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