Document Compliance Coordinator

4 weeks ago

Melbourne, Australia Bell People Consultants Full time

Global Pharmaceutical Manufacturing Organisation
- Excellent Long Term Contract Opportunity
- Melbourne Metro Area

**About the Organisation**

Operating as a multinational global healthcare manufacturing organisation with world class manufacturing facilities, our client is known for its innovation, premium quality products and strong brand reputation.

Due to continual growth and expansion, an opportunity has now arisen for a talented
**Document Compliance Coordinator with an Engineering or Science background to be responsible for SOP writing, documentation of procedures & processes, Work Instructions etc for major new facility.**

**About the Opportunity**

Reporting to the Senior Project Manager, key responsibilities include:

- Develop & maintain departmental processes including SOP's, Work Instructions. Process Flow Charts, Training.
- Assist in operational readiness for electronic batch records, development of workflows & procedures.
- Coordinate documentation reports for Building Operations & Services.
- Coordinate deviations, change controls, CAPA's & risk assessments.
- Collaborate in facility GMP & technical internal & external audits
- Effectively liaise internally with all relevant key stakeholders.

**About You**
- Tertiary qualifications in Engineering or Science.
- Minimum of 3 to 5 years of experience in quality and/or engineering. within regulated industry such as pharmaceutical, medical device.
- Sound pharmaceutical/medical device industry exp ESSENTIAL.
- Sound experience in writing/reviewing documentation including updated SOP's, WI's etc.
- Sound administration/organisational skills with the ability to prioritise.
- Strong communication & interpersonal skills.
- Ability to work in cross functional/multi disciplinary team.
- Sound MS Office skills including Word, Excel, Powerpoint.

**Culture & Opportunities**

This is an excellent contract opportunity for an
**Document Compliance Coordinator from an Engineering or Science background to join a leading global pharmaceutical manufacturing orgn**. for update of procedures & processes including SOP's, WI's etc.

**This is a long term contract opportunity with potential to convert to a permanent role. ASAP start.**

**How To Apply**

For confidential discussion, please contact Sue Campbell on 1300 793 994 or 0417 994 917.

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