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Document control specialist - pharmaceutical industry

Melbourne
beBeeValidation
Pharmaceutical industry
Posted: 17 November
Offer description

Job Opportunity:

The Commissioning, Qualification, and Validation Engineer plays a critical role in developing documentation for pharmaceutical facilities, utilities, and equipment.

Responsibilities and Expectations:

1. Protocol writing and execution at client sites
2. Development of summary reports and presentations
3. Autoclave / Parts Washer Qualification experience is essential
4. Experience in 1 or more of the following areas is desired: facilities and equipment startup, walk downs & troubleshooting, utilities (WFI, RO, HVAC), building automation or other pharmaceutical manufacturing processes and equipment, FAT/SAT, URS, design review, P&IDs, IQ/OQ/PQs, generation & execution
5. Excellent technical problem-solving and analytical skills are required
6. High attention to detail and ability to multitask
7. Ability to work independently and take initiative on assigned tasks
8. Support onsite and offsite activities such as FATs, SATs, IOQ and PQ Executions and System Walkdowns

Requirements and Qualifications:

* Bachelor's or Master's degree in a relevant science or engineering field, or equivalent years of hands-on experience
* Proficiency in Microsoft Office applications and data analysis tools
* Excellent written and verbal English communication skills
* Ability to travel domestically and internationally if required
* Eligibility to work in Australia without sponsorship

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