QA Operations - Biopharma MNC #HMS

Recruit Express Pte Ltd; Singapore; On-site; SGD 50,000 - 61,000; Part time

Job summary

Recruit Express Pte Ltd is hiring for a QA Operations role in a biopharma MNC based in Tuas. The position focuses on GMP manufacturing support, quality assurance activities, data entry and documentation in a regulated environment.

You will maintain data integrity, assist with SOP adherence, participate in 6S housekeeping, and collaborate with cross-functional teams on deviations and inspections. This is a 6-month contract with islandwide company transport available.

Qualifications

• Must follow GMP requirements and SOPs
• Experience in QA documentation and data entry
• Ability to identify deviations and report issues promptly
• Support handling of materials, components and equipment
• Maintain data integrity and proper documentation

Responsibilities

• Perform assigned operational activities in accordance with GMP requirements and SOPs
• Support QA documentation including data entry, document review, form submissions and document management
• Identify and promptly report deviations, non-conformances and safety concerns
• Support the handling of materials, components and equipment according to established procedures
• Maintain accurate documentation and uphold data integrity principles
• Assist with routine housekeeping, cleaning and 6S activities to maintain a compliant work environment
• Participate in relevant training for assigned tasks
• Work closely with team members, supervisors and cross-functional stakeholders
• Maintain confidentiality and integrity of operational and company information
• Support other operational activities as assigned

Skills

GMP knowledge

SOP compliance

Data integrity

QA documentation

Cross-functional teamwork

Tools

Document management system

Job description

QA Operations - Biopharma MNC

Tuas | Islandwide Company Transport Available
6-Month Contract
QA / GMP Manufacturing Environment

Key Responsibilities

• Perform assigned operational activities in accordance with GMP requirements and SOPs
• Support QA documentation including data entry, document review, form submissions and document management
• Identify and promptly report deviations, non-conformances and safety concerns
• Support the handling of materials, components and equipment according to established procedures
• Maintain accurate documentation and uphold data integrity principles
• Assist with routine housekeeping, cleaning and 6S activities to maintain a compliant work environment
• Participate in relevant training for assigned tasks
• Work closely with team members, supervisors and cross-functional stakeholders
• Maintain confidentiality and integrity of operational and company information
• Support other operational activities as assigned