QA Specialist (Validation)

Job Summary:

The role is responsible for planning, executing, and maintaining validation and qualification activities for equipment, utilities, facilities, processes, and computer systems to ensure compliance with regulatory and GMP standards. Key responsibilities include preparing and reviewing qualification documents (URS, DQ, IQ, OQ, PQ), process and cleaning validation protocols, managing deviations and CAPAs, and ensuring validated states are sustained.

The position works closely with cross-functional teams and external service providers to meet validation schedules and support continuous improvement in validation practices. It also provides QA oversight, performs risk assessments for changes, and contributes to updates of the Validation Master Plan and related SOPs.

Qualifications:

• Degree in a scientific discipline or related field.
• 57 years of relevant validation experience in a pharmaceutical manufacturing environment.
• Strong knowledge of qualification/validation principles, regulatory compliance, and documentation practices.
• Proficient in Microsoft Office applications.

To Apply:

Candidates are encouraged to apply this position via email to [Confidential Information] with the following information in the resume.

• Work experiences and job responsibilities.
• Current and Expected salary
• Reason for leaving.
• Date of availability
• Education background

We regret that only shortlisted candidates will be contacted.