Validation Associate - Melbourne, Australia - Bell People Consultants

Bell People Consultants
Bell People Consultants
Verified Company
Melbourne, Australia

2 weeks ago

Olivia Brown

Posted by:

Olivia Brown

beBee Recruiter
Description
Global Pharmaceutical Organisation

  • Excellent Long Term Contract Opportunity
  • Melbourne Metropolitan Area

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 in the healthcare industry, is now seeking a

Validation Associate to provide support for projects including TGA compliance as well as revalidation activities.


About the role

Key duties & responsibilities include the following:

  • Perform the validation activities for processes, cleaning or equipment as required for allocated projects.
  • Plan, coordinate & monitor validation activities in accordance with Quality Management system, Site Validation Master Plan and validation procedures.
  • Prepare, implement & maintain departmental documentation for validation activities & regulatory submissions.
  • Prepare, review, implement & maintain departmental documentation for validation activities.
  • Build & maintain strong collaborative relationships with key stakeholders.

About you

  • Tertiary qualifications in Science or Engineering.
  • Specific experience in validation in the pharmaceutical/medical device industry within a GMP environment.
  • Demonstrated knowledge of GMP, QMA & Risk Management.
  • Sound knowledge of industry documents, standards & validation principles.
  • Sound communication & interpersonal skills.
  • Excellent attention to detail.

Culture & Benefits
This is an excellent opportunity for a

Validation Associate with specific experience in validation to further develop their skills and experience within a large pharmaceutical organisation.

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

PLEASE SUBMIT MS WORD DOCUMENTS ONLY
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