Position Description

Quality Validation Officer (1-year contract/ Pharmaceutical/ no experience required)
Job Code 16504
Division GMP TECHNOLOGIES (S) PTE LTD (EA Licence:11C3793)
Job Placement Location Singapore
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Responsibilities

  • Participate/ lead in the conduct of audits on equipment / system, and internal cross-functional departments involved in the manufacture of bulk drug substances.
  • Draft, compile, review and update appropriate policies and procedures in support of the validation activities on site.
  • Assess, review and approve changes that may have an impact on the validation status of the facility, processes or systems on site
  • Participate as an audit team member and/or as a subject matter expert in the preparation of site audits by internal corporate groups and external
  • Act as a Validation Coordinator in projects that are deemed to have

 

Requirements

  • Degree in science and engineering discipline.
  • Candidate with at least 5 years’ experience will be considered Senior Quality Validation Officer.
  • Candidate without experience or preferably with 1 – 2 years of experience are welcome to apply.

 

To apply, please visit to www.gmprecruit.com

To find out more about this opportunity, please contact Lionel Liew at lionel.liew@gmprecruit.com.

 

We regret that only shortlisted candidates will be notified.

 

GMP Technologies (S) Pte Ltd   |   EA Licence: 11C3793 |   EA Personnel: Lionel Liew   |   Registration No: R1330693

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