Job Description

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Validation Associate

Advertiser: TechstaffMore jobs from this company

Job Information

Job Listing Date
7 Dec 2018
Location
Melbourne, Bayside & South Eastern Suburbs
Work Type
Contract/Temp
Classification
Science & Technology, Quality Assurance & Control
Validation Associate
  • Outstanding Opportunity for a Validation Professional
  • Global Nutraceutical Company / Brand New Facility
  • Located in the SE Suburbs / 12 month contract

The Company


Our client is a leading international health supplement contract manufacturer expanding its global operations with a new purpose built, 'state of the art' complimentary medicine production facility in the South Eastern Suburbs. As part of their new venture, they seek to appoint a suitably qualified and experienced Validation Associate to join their Quality team.

The Role

Working closely with the QA Validation Manager, you will have the following responsibilities:

  • Support the QA department to perform validation and qualification of equipment and processes, operator training, SOP creation etc according to internal procedures and GMP
  • Perform validation testing of raw materials, intermediate and finished products
  • Proficient in preparing and reviewing qualification documents and summary qualification reports
  • Analyse validation data to determine if systems and processes have met validation criteria / standards and perform root cause analysis of any production problems determined
  • Carry out validation audits and / or performance qualification processes to ensure compliance with company and regulatory standards
  • Development and maintenance of validation tracking databases for activity, test results and validation systems

Personal Attributes, Qualifications & Relevant Experience

To succeed in this exciting role, you will possess:

  • BSc and previous relevant experience within the pharmaceutical, manufacturing or related environment
  • Excellent written and verbal communication skills, together with demonstrated problem solving and time management skills
  • Through understanding of the regulatory requirements (e.g. TGA and PIC/S)
  • Proven experience working within a GMP quality environment
  • Positive, proactive, professional attitude
  • Ability to build strong cross functional working relationships is necessary
  • A desire to grow with this company

The Rewards

If you want to join a progressive and socially responsible organisation, with the vision of becoming a major contributor to the growth and reputation of the business, then this role is for you.

To submit your application in strict confidence, click the 'apply' button. If you require further information, please contact Voula Triantafillou on 03 9864 6050.

To view all Techstaff job opportunities visit www.techstaff.com.au

The Company


Our client is a leading international health supplement contract manufacturer expanding its global operations with a new purpose built, 'state of the art' complimentary medicine production facility in the South Eastern Suburbs. As part of their new venture, they seek to appoint a suitably qualified and experienced Validation Associate to join their Quality team.

The Role

Working closely with the QA Validation Manager, you will have the following responsibilities:

  • Support the QA department to perform validation and qualification of equipment and processes, operator training, SOP creation etc according to internal procedures and GMP
  • Perform validation testing of raw materials, intermediate and finished products
  • Proficient in preparing and reviewing qualification documents and summary qualification reports
  • Analyse validation data to determine if systems and processes have met validation criteria / standards and perform root cause analysis of any production problems determined
  • Carry out validation audits and / or performance qualification processes to ensure compliance with company and regulatory standards
  • Development and maintenance of validation tracking databases for activity, test results and validation systems

Personal Attributes, Qualifications & Relevant Experience

To succeed in this exciting role, you will possess:

  • BSc and previous relevant experience within the pharmaceutical, manufacturing or related environment
  • Excellent written and verbal communication skills, together with demonstrated problem solving and time management skills
  • Through understanding of the regulatory requirements (e.g. TGA and PIC/S)
  • Proven experience working within a GMP quality environment
  • Positive, proactive, professional attitude
  • Ability to build strong cross functional working relationships is necessary
  • A desire to grow with this company

The Rewards

If you want to join a progressive and socially responsible organisation, with the vision of becoming a major contributor to the growth and reputation of the business, then this role is for you.

To submit your application in strict confidence, click the 'apply' button. If you require further information, please contact Voula Triantafillou on 03 9864 6050.

To view all Techstaff job opportunities visit www.techstaff.com.au

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