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Company Info

Healthcare Professionals Group



Phone: (02) 8877 8777 (03) 9938 7100
Web Site: https://www.hpgconnect.com/

Company Profile


Quality Systems Manager - Biotechnology


col-narrow   

Posted:

16.04.2019

Employment Type:

Contractor

Location:

Melbourne CBD, VIC 

Title:

Quality Systems Manager - Biotechnology

Category:

Quality/Validation
col-wide   

Job Description:

About the company

This global biotechnology company is committed to bringing its disruptive cellular medicine to patients in order to treat serious and life threatening conditions

About the opportunity

In this busy contract position; you will be responsible for the maintenance of Quality Management Systems for this unique biotechnology company.

Duties

  • Managing new and current documents in compliance with pharmaceutical regulatory requirements
  • Develop and review GxP documentation
  • Management and organisation of controlled documentation and quality records
  • Actively provide consultation in regard to document control to ensure continual compliance with QA
  • Management of the Quality Management Review and training process for all staff

Skills and Experience

  • Tertiary qualification in life sciences
  • Previous experience and working knowledge of TGA and FDA requirements
  • Ability to work under pressure with strong problem solving skills
  • Demonstrated experience in working cross functionally
  • Be flexible and agile in your approach to work
  • Highly developed interpersonal skills

How to Apply

Click apply or contact Jo Turner (Senior Specialist Manager) on 03 9938 7120 for a confidential discussion.



( SK915725A )



Company Info


Healthcare Professionals Group

Phone: (02) 8877 8777 (03) 9938 7100
Web Site: https://www.hpgconnect.com/

Quality Systems Manager - Biotechnology

col-narrow   

Posted:

16.04.2019

Employment Type:

Contractor

Location:

Melbourne CBD, VIC 

Title:

Quality Systems Manager - Biotechnology

Category:

Quality/Validation
col-wide   

Job Description:

About the company

This global biotechnology company is committed to bringing its disruptive cellular medicine to patients in order to treat serious and life threatening conditions

About the opportunity

In this busy contract position; you will be responsible for the maintenance of Quality Management Systems for this unique biotechnology company.

Duties

  • Managing new and current documents in compliance with pharmaceutical regulatory requirements
  • Develop and review GxP documentation
  • Management and organisation of controlled documentation and quality records
  • Actively provide consultation in regard to document control to ensure continual compliance with QA
  • Management of the Quality Management Review and training process for all staff

Skills and Experience

  • Tertiary qualification in life sciences
  • Previous experience and working knowledge of TGA and FDA requirements
  • Ability to work under pressure with strong problem solving skills
  • Demonstrated experience in working cross functionally
  • Be flexible and agile in your approach to work
  • Highly developed interpersonal skills

How to Apply

Click apply or contact Jo Turner (Senior Specialist Manager) on 03 9938 7120 for a confidential discussion.



( SK915725A )

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