Not specified (could be inferred as hybrid or onsite based on industry norms).
Gmp-regulated environment experience
Dq iq oq pq documentation knowledge
Temperature mapping and calibration
No Deviation PTE. LTD. is seeking a Validation Support professional to assist with validation lifecycle activities in a regulated pharmaceutical environment. The ideal candidate will contribute to maintaining compliance with GMP standards while enjoying a collaborative culture that emphasizes empathy, integrity, and continuous development
Job Summary
The role supports validation lifecycle activities across direct, indirect, and no-impact systems within a regulated pharmaceutical environment.
Responsibilities include generating, reviewing, and approving validation documentation such as DQ, IQ, OQ, and PQ for new equipment qualification.
The company offers generous leave policies, comprehensive health coverage, and professional development opportunities in an inclusive culture.
Matching Summary
Match Score: 85
No Deviation PTE. LTD. is seeking a Validation Support professional to assist with validation lifecycle activities in a regulated pharmaceutical environment. The ideal candidate will contribute to maintaining compliance with GMP standards while enjoying a collaborative culture that emphasizes empathy, integrity, and continuous development.
Skills & Requirements
Must-have
GMP-regulated environment experience
DQ IQ OQ PQ documentation knowledge
Temperature mapping and calibration
Nice-to-have
Cross-functional stakeholder coordination
Strong attention to detail
Collaborative team culture
Key Requirements
Diploma or Degree in Engineering, Life Sciences, Pharmacy, or related field
Experience in validation or qualification within GMP-regulated environments
Understanding of temperature mapping and equipment qualification processes