Validation Engineer, CSV (Pharmaceutical) - #1128987

Responsibilities

• Deliver consulting projects in process-related areas, including but not limited to Equipment Qualification, Computer System Validation (CSV), and other qualification and validation disciplines.

• Prepare CQ deliverables such as User Requirement Specifications (URS), risk assessments, data integrity assessments, and qualification/validation protocols.

• Execute CQ protocols including temperature mapping and CSV testing/verification.

• Support business development and service initiatives as directed by the management.

Requirements

• Bachelor’s Degree in Life Sciences, Engineering, or a related discipline.

• Minimum 2 years of relevant experience in the pharmaceutical, medical device, or related regulated environment.

• Fresh graduates with internship experience in the pharmaceutical or medical device industry and relevant exposure may be considered for a Junior role.

• Good understanding of regulatory requirements and industry best practices (GxP, validation lifecycle, data integrity).

• Hands-on experience with Kaye Validator or Ellab temperature mapping systems is an added advantage.

• Familiarity with ASTM E2500 practices will be preferred.

Interested candidates please apply online or send your latest CV to [email protected]

AlwaysHired Pte Ltd

Reg No: R1549345

EA: 24C2293

We regret to inform that only shortlisted candidates will be notified. Please note that your response to this advertisement will constitute informed consent to the collection, use, and/or disclosure of personal data by AlwaysHired, its affiliates and, where necessary, to relevant third parties, for purposes such as job application processing, career advisory, research, and other administrative purposes, in compliance with the relevant provisions of the Privacy Policy available at www.alwayshired.com.sg/privacy-policy