Quality Validation Officer (Pharmaceutical Manufacturing) - #1165993
GMP Group
Job Description
Purpose: Support validation and quality activities to ensure manufacturing processes, equipment, and systems comply with GMP and regulatory requirements, under guidance from senior validation or QA staff.
Job scope:
Support validation activities for equipment, processes, cleaning, and systems in accordance with approved protocols and procedures.
Assist in drafting, reviewing, and maintaining validation documentation, SOPs, and reports.
Support change control assessments to identify potential impact on validation and product quality.
Review validation protocols and reports for completeness and GMP compliance.
Participate in internal audits and regulatory inspections as a supporting team member.
Assist in deviation investigations, including documentation review and impact assessment on validation status.
Support validation activities for new projects and New Product Introduction (NPI) under supervision.
Assist in periodic review of validated systems and support Continued Process Verification (CPV) documentation.
Support cleaning and method validation activities by coordinating documentation and data review.
Provide basic QA support for engineering activities such as preventive maintenance deviations and GxP documentation tracking.
Requirements:
Min. Bachelors Degree in Analytical chemistry, chemical engineering, chemistry, pharmaceutical sciences or related discipline
Min. 1-2 years of experience in validation, QA, or manufacturing support within a pharmaceutical, biotech, or regulated manufacturing environment
Good knowledge of GMP and validation
Good knowledge of quality and manufacturing process knowledge
Basic knowledge of corporate management systems
Good knowledge of regulatory processes and audit
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We regret that only shortlisted candidates will be notified.
GMP Technologies (S) Pte Ltd
EA License: 11C3793 | Personnel: Dianna @ dia•••@gmprecruit.com I Registration No: R1327268
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