Validation Associate

About the Role:


The purpose of this role is to support and perform validation activities in regards to new and existing processes, as well as projects. The main responsibilities may include:

• Perform the validation activities associated with changes to plant, equipment and processes
• Participate in equipment and manufacturing validation
• Perform validation activities in accordance with the Quality Management system
• Prepare, implement and maintain department documentation
• Validation protocol and reports
• Actively participate in problem solving and identify opportunities for improvement to optimise validation activities

About You:

• Bachelor Degree in a relevant Science or Engineering discipline
• Experience in the pharmaceutical manufacturing industry (highly regarded)
• Knowledge of industry guidance documents and standards, with a good understanding of validation principles
• Understanding of GMP
• Excellent communication skills
• Ability to multi task
• Strong computer literacy skills

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.