QMS Engineer [Pharma MNC | $3800 | Joo Koon] RRKC

Rapid Recruitment Asia Pte Ltd; Singapore; On-site; SGD 39,000 - 46,000; Full time

Benefits offered by this job

1-month bonus

Job summary

US Pharmaceutical Company @ Joo Koon is seeking a Quality Assurance/Quality Management professional for a 12-month contract in Singapore. The role focuses on developing and maintaining SOPs, managing QMS processes, and ensuring cGMP compliance.

You will coordinate internal audits, audit readiness, and support external audits while driving data integrity and continuous improvement across the site.

Qualifications

• Degree in Life Sciences, Chemical/Biochemical Engineering, Pharmaceutical Science or related fields.
• 2 years of Quality Assurance/Quality Management experience in the pharmaceutical industry preferred.
• Knowledge of cGMP, regulatory compliance and QMS.
• Experience in biologics, aseptic processes, data integrity or pharmaceutical manufacturing is an advantage.
• Good problem-solving and Quality Risk Management skills.
• Strong communication, coordination and teamwork skills.

Responsibilities

• Develop, review and maintain SOPs, work instructions and quality documents.
• Manage key QMS processes including Change Control, CAPA, document control and training.
• Ensure compliance with cGMP, regulatory requirements and company quality standards.
• Coordinate site self-inspections, internal audits and audit readiness activities.
• Support client and regulatory audits, including follow-up and closure of audit findings.
• Manage GMP training programmes and support employee qualification requirements.
• Conduct Product Quality Reviews (PQR) and quality trend analysis.
• Support supplier quality activities, including Quality Agreements and supplier evaluations.
• Monitor QMS activities and ensure quality events and actions are completed on time.
• Support data integrity and continuous improvement initiatives.
• Prepare quality metrics and reports for management review.
• Promote a strong safety and quality culture across the site.
• EHS Responsibilities: Follow and promote workplace health, safety and environmental requirements.
• Understand and follow emergency procedures and safe working practices.
• Promptly report and support investigations of accidents, near misses and safety incidents.

Skills

Quality Assurance

QMS

cGMP

CAPA

Audit readiness

Data integrity

Regulatory compliance

Communication

Teamwork

Education

Life Sciences / Chemical or Biochemical Engineering / Pharmaceutical Science degree

Job description

Job Summary

• US Pharmaceutical Company @ Joo Koon

• Monday - Friday, 8AM to 5:15PM

• 12-Months Contract

• Up to $3,800/month + 1-month bonus

Key Responsibilities

• Develop, review and maintain SOPs, work instructions and quality documents.

• Manage key QMS processes including Change Control, CAPA, document control and training.

• Ensure compliance with cGMP, regulatory requirements and company quality standards.

• Coordinate site self-inspections, internal audits and audit readiness activities.

• Support client and regulatory audits, including follow-up and closure of audit findings.

• Manage GMP training programmes and support employee qualification requirements.

• Conduct Product Quality Reviews (PQR) and quality trend analysis.

• Support supplier quality activities, including Quality Agreements and supplier evaluations.

• Monitor QMS activities and ensure quality events and actions are completed on time.

• Support data integrity and continuous improvement initiatives.

• Prepare quality metrics and reports for management review.

• Promote a strong safety and quality culture across the site.

• EHS Responsibilities

• Follow and promote workplace health, safety and environmental requirements.

• Understand and follow emergency procedures and safe working practices.

• Promptly report and support investigations of accidents, near misses and safety incidents.

Requirements

• Degree in Life Sciences, Chemical/Biochemical Engineering, Pharmaceutical Science or related fields.

• 2 years of Quality Assurance/Quality Management experience in the pharmaceutical industry preferred.

• Knowledge of cGMP, regulatory compliance and QMS.

• Experience in biologics, aseptic processes, data integrity or pharmaceutical manufacturing is an advantage.

• Good problem-solving and Quality Risk Management skills.

• Strong communication, coordination and teamwork skills