Candidates must be flexible to work between the hours of 7.30am and 4pm.
The role will be a 38-hour week with occasional overtime and weekend work.
Standard 8-hour shifts.
Your duties:
Preparation and approval of new GMP documentation
Participate in all GMP audits for new products and perform follow up actions as needed
Establish training requirements for production staff for new and changed processes
Solution preparations
Perform commissioning, qualification and validation tasks as needed
Participate in all GMP audits for new products and perform follow up actions as needed
Plant and equipment cleaning and sterilization
Monitoring of cultures in small & large scale bio-reactors
Downstream processing and purification of antigens
Implement training plans to ensure smooth introduction of new products and processes
Provide technical assistance for manufacturing operations for new processes
About you:
Strong understanding of GMP and cleanroom environments
Tertiary qualification in Microbiological Science, Engineering or related discipline is desirable
Demonstrated experience in a similar role within the Pharmaceutical/Food industry.
Strong communication skills
Knack for quick learning
Goes above and beyond
Apply! 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 Deborah or Sarah 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.