
Validation Associate
2 days ago
Our client, leading research-based biopharmaceutical company, is seeking a Validation Associate to join their team in Melbourne.
**Your responsibilities will include**:
- Drafting of User Requirement Specifications (URS) for new instrumentation and/or software.
- Drafting and execution of validation test protocols (IQ,OQ and PQ) for new instrumentation and/or software.
- Drafting of Validation Summary Reports on completion of validation activities for new instrumentation and/or software
- Assist with the development and review of procedures required for usage, calibration, verification, and maintenance of new laboratory instrumentation
- Support team colleagues as required
**Other Position Requirements include**
- BSc or MSc in Microbiology or related field
- Proven experience in pharmaceutical/microbiology environment
- A knowledge of cGMP/GLP and Regulatory requirements for pharmaceutical industry
- Experience with environmental monitoring test requirements
- Experience with microbial identification testing (eg Bruker or Vitek systems)
- Well organized, with high personal commitment, accountability and motivation and an ability to work independently on projects with tight project timelines.
- Strong verbal and written communications skills.
- Well-developed technical problem solving and analytical skills.
- Strong interpersonal, communication and team-work skills.
**Who are we**
At PERSOLKELLY, our passion is - and always has been - putting you first.
We propel our people forward by supporting their careers in fresh ways, backed by our expertise and capability.
We're committed to creating a safe and inclusive environment which values and respects diverse styles, backgrounds, experience and perspectives.
We welcome and encourage women, people of Aboriginal and Torres Strait Islander descent and people from diverse backgrounds to apply.
**So it's over to you. If you would like to join our team, please APPLY now.**
**To learn more about working with PERSOLKELLY, we encourage you to visit our website.
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