Manage the site's regulatory inspections and internal audits
Manage preparations for internal and external audits
Manage and report on CAPAs performance
Initiate and manage impact assessments, reporting of new regulatory requirements to maintain and improve site compliance
Maintain the self-inspection schedule, lead audits to meet self-inspection schedule
Create and update quality agreements as required
Author APQR, maintain and update APQR schedule, support APQR forum/presentation
Skills/experience:
Tertiary education in Science, Engineering, Pharmaceutical Science or similar
Proven experience in a QA-related role within pharmaceutical, biotech or other highly regulated environment
Background in Microbiology or Biochemistry would be highly advantageous
Good interpersonal, analytical and problem-solving skills
Ability to work well independently and in a team
Great organisational and time management skills
Excellent verbal and written communication skills
Apply! If you think this could be the role for you then please apply now! Please send us a cover letterAND a detailed resume in WORD format (PDFs can be corrupted / not processed). Or, if you have any questions, please contact Linda on 03 9040 1630.
With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.
Submission Form
Submit your message along with your CV attached, and one of our specialists will be in touch.