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Quality Validation Officer - Csv In Pharmaceutical (1 Year Contract)

GMP Technologies (S) Pte Ltd

D01 Marina, Raffles Place, People's Park, CecilContractS$5,500 – S$7,000/mo

Posted 15 Jul 2026

About this role

Job Description & Requirements Job Purpose To ensure manufacturing facilities, processes, analytical methods, and systems are validated in compliance with cGMP and regulatory requirements , ensuring consistent product quality in accordance with established specifications. Key Responsibilities Participate in and/or lead GMP audits of equipment, systems, processes, and cross-functional departments Prepare, review, and maintain validation-related SOPs, policies, and procedures Assess and approve changes (Change Control) that may impact product quality, compliance, or validation status Review, approve, and authorize validation protocols and reports Support and participate in internal, corporate, and regulatory audits as a validation SME Conduct investigations related to complaints, deviations, recalls, or failures; assess root causes and CAPA impact on validation Act as Validation Coordinator for projects with product quality impact, including chairing validation meetings Provide QA support for New Product Introduction (NPI) to ensure GMP compliance Lead and manage Cleaning Validation activities Perform periodic validation reviews , recommend re-validation when required, and approve Continued Process Verification (CPV) documents Support and coordinate Method Validation activities, where applicable Provide quality oversight on engineering compliance , including PM deviations, data management, and GxP spare parts/consumables Technical & Professional Skills Strong knowledge of GMP, Computer System Validation and validation principles Good understanding of manufacturing and quality systems Familiarity with regulatory requirements and audit processes Good audit, documentation, and investigation skills Basic understanding of corporate quality management systems To find out more about this opportunity, please contact Dianna at dianna@gmprecruit.com . We regret that only shortlisted candidates will be notified. GMP Technologies (S) Pte Ltd | EA License: 11C3793 | EA Personnel: Dianna| Registration No: R1327268

What they're looking for

provide proceduresCompany Auditsspecific purposesLeadership

About GMP Technologies (S) Pte Ltd

Industry: Administrative & support services

Frequently asked questions

What does a Quality Validation Officer - Csv In Pharmaceutical (1 Year Contract) at GMP Technologies (S) Pte Ltd do?

Job Description & Requirements Job Purpose To ensure manufacturing facilities, processes, analytical methods, and systems are validated in compliance with cGMP and regulatory requirements , ensuring consistent product quality in accordance with established specifications. Key Responsibilities Partic…

What skills does this Quality Validation Officer - Csv In Pharmaceutical (1 Year Contract) role need?

Key skills for this role include provide procedures, Company Audits, specific purposes, Leadership.

How much does a Quality Validation Officer - Csv In Pharmaceutical (1 Year Contract) at GMP Technologies (S) Pte Ltd pay?

This role lists a salary of S$5,500 – S$7,000 per month.

Is this Quality Validation Officer - Csv In Pharmaceutical (1 Year Contract) role remote, hybrid, or on-site?

The listing is based in D01 Marina, Raffles Place, People's Park, Cecil. Check the posting for remote or hybrid options.

How do I apply for this Quality Validation Officer - Csv In Pharmaceutical (1 Year Contract) role?

You can apply directly on GMP Technologies (S) Pte Ltd's careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.