Validation Analyst

13 hours ago

Melbourne, Australia Bell People Consultants Full time

Global Pharmaceutical Organisation
- Long Term Contract Opportunity
- Melbourne Metro - Hybrid Role - WFH & Office Based

**About The Company**

Operating as a major global Multinational pharmaceutical manufacturer with global sites worldwide, our client is well known for its growth and innovation and is an Australian iconic brand in the marketplace, offering a range of healthcare products to local & global markets.

Due to ongoing project work our client is now seeking a
**Validation Analyst **to provide support for projects & maintain the schedule for Projects with Validation involvement.

**About The Opportunity**

Reporting to the Validation Manager, key duties include the following:

- Plan, coordinate & execute validation activities in accordance with the Quality Management System, Site Validation Master Plan.
- Perform validation activities for project work.
- **Provide CSV Computer Systems Validation) deliverables including reports, plan & specifications.**:

- Plan & coordinate all computer systems validation activities including the drafting & review of all key validation documentation.
- Review various regulatory risk assessments & protocols in relation to computer system validation practices.
- Effectively liaise with key local & global stakeholders.

**About You**
- Tertiary qualifications in Science, Engineering or Computer Science.
- Specific experience in validation in the pharmaceutical/medical device industry within a GMP environment.
- **Sound understanding of computerised systems validation or process validation the pharmaceutical industry.**:

- Strong verbal & written communication skills.
- Good presentation, interpersonal & time management skills.

**Culture & Benefits**

This is an excellent opportunity for a
**Validation Analyst with sound computer systems validation (CSV) experience to further develop their skills & experience within CSV & be involved in a variety of local & global projects.**

Specific knowledge of validation protocols for validation is essential as well as a sound understanding of manufacturing and GMP 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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