Address- Well know pharmaceutical company
- Open to WHV with experience in Validation
- 6 months contract, On-site
- Monday to Friday with standard working hours
- Compliance activities relating to the qualification and validation program for the manufacturing facility and testing labs
- Management of review and approval of key GMP documentation
- Liaise with R&D departments regarding quality related issues
- Provide compliance specialist advice on qualification and validation issues
- Actively participate in problem solving and identifying opportunities for improvement
- A degree in a relevant science, validation or engineering discipline
- Understanding of GMP requirements in the pharmaceutical industry and previous experience within the pharmaceutical industry including qualification and validation principles and applications
- Good interpersonal, analytical and problem solving skills
- Ability to work well independently and in a team.
- Great organizational and time management skills
If you think this could be the role for you then please apply now! Please send us a cover letter AND a detailed resume in WORD format (PDFs can be corrupted / not processed).
Or, if you have any questions, please contact Sarah or Priyanka on 03 9040 1***
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.
