QUALITY ASSURANCE OFFICERS (Pharmaceuticals Manufacturing - GMP)

Hamilton, Waikato, New Zealand - 171001 - POSTED 25/01/2018

Our client is a fast growing company in the developmental stages of producing an exciting new product to supply both Animal Remedy and Human Therapeutic Markets.Progression on this product has reached the clinical trial stage with the Hamilton Plant responsible for supplying both Asian and European markets. All processing activities have been carried out in a GMP compliant environment.
We have an exciting opportunity for two GMP experienced Quality Assurance officers to be part of the QA team's transition to full GMP compliance
The Person:
  • At least 2-3 years QA experience in GMP pharmaceutical manufacturing industry
  • University graduate or above in pharmaceutical science, QA, chemical and biological disciplines
  • Knowledge in pharmaceutical regulations and standards
  • A self-starter with excellent time management skills, visionary with shared goals, willing to learn and develop others, meticulous, hardworking and team collaboration focused
  • Good interpersonal skills
  • Great communication skills in both oral and written English
If this sounds like you then send me your CV in confidence and I will schedule a time to meet and discuss your suitability further
Salary $55k - $65k per year with additional benefits
The Job:
  • Facilitate the qualification and validation system; review and approve the related technical documents
  • Assist in the development, implementation and maintenance of our Quality Management System in accordance with GMP Principles and RMP requirements
  • Ensure all products are consistently produced and controlled to the defined quality standards
  • Ensure all corporate quality policies and standards are adhered to by all staff at New Zealand manufacturing site
  • Be responsible for working with the QAM in the drafting, reviewing, approving and controlling of quality documentation such as Standard Operation Procedures (SOP) and other quality system documents
  • e responsible for working with the QAM in the preparation of Management Review Reports, Product Quality Review (PQR) Reports, Quality Manual, Validation Master Plan, Site Master File and other site related Quality Documents
  • Manage timely completion of self – inspections and external audits and vendor
Apply Now
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