Quality Validation Officer (1 year contract) | Pharma MNC | West (Urgent)

GMP TECHNOLOGIES (S) PTE LTD; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A leading pharmaceuticals company in Singapore is looking for a Validation Support specialist. The role includes supporting validation activities for equipment and processes, assisting in documentation reviews, and participating in audits. Ideal candidates should have a Bachelor's degree and 1-2 years of experience in validation or QA. Applicants with no prior experience will also be considered. Competitive salary and opportunities for growth are provided.

Qualifications

• Min. 1-2 years of experience in validation, QA, or manufacturing support.
• Good knowledge of GMP and validation processes.
• Basic knowledge of corporate management systems.

Responsibilities

• Support validation activities for equipment and processes.
• Assist in drafting validation documentation and SOPs.
• Participate in internal audits and regulatory inspections.

Skills

Validation

Quality Assurance

GMP knowledge

Manufacturing support

Regulatory processes

Education

Bachelor's Degree in Analytical Chemistry or related discipline

Job description

Jobscope

• 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
• Candidates with no prior experience will be considered

To find out more about this opportunity, please contact Fiona Koh

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh | Registration No: R1109239
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This is in partnership with the Employment and Employability Institute Pte Ltd (e2i).

e2i is the empowering network for workers and employers seeking employment and employability solutions. e2i serves as a bridge between workers and employers, connecting with workers to offer job security through job-matching, career guidance and skills upgrading services, and partnering employers to address their manpower needs through recruitment, training, and job redesign solutions. e2i is a tripartite initiative of the National Trades Union Congress set up to support nation-wide manpower and skills upgrading initiatives.

By applying for this role, you consent to GMP Recruitment Services (S) Pte Ltds PDPA and e2is PDPA.