QA Specialist (Validation) - #1126839

Pharmagend Global Medical Services Pte Ltd


Date: 5 days ago
District: Tuas
Contract type: Full time
Work schedule: Full day
Pharmagend Global Medical Services Pte Ltd

KEY DUTIES AND RESPONSIBILITES:

  • Preparation and review of qualification documents e.g., User requirement specification, DQ, IQ, OQ and PQ protocol for equipment, utilities & facility in compliance with the regulatory guidelines.

  • Execution of qualification and validation activities including process, cleaning, computer system, equipment, utilities, and facility.

  • Candidate must have knowledge and experience of qualification/validation principles and their practical application.

  • Preparation and review of process and cleaning validation protocols and reports.

  • Coordinate with the cross functional team and external service provider to meet qualification & validation schedules and maintain equipment, systems, and processes in validated state.

  • Review equipment and process related change control; perform Risk Assessment to determine criticality of the proposed changes.

  • Write, review, and revise validation SOPs in compliance with regulatory guidelines.

  • QA oversight and/or review during the validation process.

  • Manage incidents and deviations related to validation & qualification.

  • Perform compliance reviews of all applicable deviations, investigations, and CAPAs related to qualification and validation.

  • Review and suggest continuous improvements to the Validation Master Plan, current quality system practices, validation protocols and procedures for newly installed equipment, and overall validation strategies.

  • Cross train and develop expertise in other areas of validation. 

  • Must be able to interact and lead effectively in a team-based environment.

  • Familiarity with regulatory/compliance environment.


EDUCATION & EXPERIENCE

  • Degree a scientific discipline or equivalent.

  • Experience in a regulated industry preferred.

  • Proficient in the use of Microsoft Word, Excel, Access, PowerPoint, and Explorer.

  • A minimum of 5-7 years’ relevant experience in pharmaceutical manufacturing environment.
     

We regret that only shortlisted candidates will be contacted.

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