Validation Specialist
7 days ago
Global Pharmaceutical Manufacturing Organisation
- Excellent Contract Opportunity - Start ASAP
- Melbourne Metropolitan Area
**About the Organisation**
Operating as a global Multinational pharmaceutical manufacturer, our client is well known for its growth and innovation and is an Australian iconic brand in the marketplace.
Due to ongoing project work, our client is now seeking a **Validation Specialist **with experience in process, equipment or facility validation for qualification & commissioning activities for Equipment, Facilities & Processes.
**About the Opportunity**
Key duties & responsibilities include the following:
- Manage qualification & commissioning of equipment, facilities & processes.
- Plan, coordinate & execute validation activities in accordance with the Quality Management System, Site Validation Master Plan.
- **Prepare & execute validation protocols in process validation, equipment validation or facility validation.**:
- Participate in equipment & manufacturing validation.
- Effectively liaise with QC, QA, Engineers & the overall Validation Team.
**About You**
- Tertiary qualifications in Science or Engineering.
- Industry experience in the pharmaceutical/medical device industry.
- **Experience in process, equipment or facility validation.**:
- Sound knowledge of validation protocols, validation plans & the appropriate GMP documentation.
- Ability to resolve issues independently.
- Must be a self starter & able to solve problems.
**Culture & Benefits**
This is an excellent opportunity for a **Validation Specialist** **to join global pharmaceutical organisation & be responsible for a wide range of validation activities.**
Specific knowledge of validation protocols within pharmaceutical industry is essential as well as good knowledge of manufacturing and cGMP principles.
**How To Apply**
For a confidential discussion on this opportunity, please contact Sue Campbell on 0417 994 917 or Maria Julienne on 0491 694 371.
PLEASE SUBMIT MS WORD DOCUMENTS ONLY
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