Experience in Implementation of ISO 13485 or USFDA Documentation. Strong analytical and instrumentation skills.
Strong Coordination In preparation of System documentation from production to Dispatch.
Supports supplier issue resolution, by providing product specific knowledge/understanding.
Required Experience, Skills and Qualifications
B.Sc. or M.Sc. degree in Chemistry, Microbiology or a related science, B-Pharmacy, M-Pharmacy or Related Qualification in Material Engineering.
Should have experience in food packaging, pharma, health care, medical packaging / Devises or Hospitals.
GMP ( Good Manufacturing Practice ) experience in the areas of quality control/compliance and validation.
2 - 3 years at a supervisory level, including responsibility for department and staff administration; previous direct validation experience or participation in validation workgroup activities, QA/QC compliance activities, and/or compliance audit experience.