Senior QA Specialist – cGMP Compliance & Validation Lead

No deviation Pte Ltd.; Singapore; Hybrid; SGD 110,000 - 160,000; Full time

Job summary

No deviation Pte Ltd. in Singapore seeks a QA Senior Specialist to advance day-to-day quality assurance activities across cGxP contract manufacturing.

You will review SOPs, participate in deviations, CAPA, audits, and change controls, ensuring data integrity and compliance with regulatory standards. Responsibilities span QA validation, technical compliance, and cross-functional collaboration with QC, Engineering, and Validation teams to release products on time while maintaining the highest

Qualifications

• Bachelor's Degree in Life Sciences, Pharmaceutical Sciences, Biotechnology, Chemistry, Engineering, or related discipline.

Responsibilities

• Support day-to-day Quality Assurance activities in accordance with approved SOPs / Policies for a multi-product, cGxP contract manufacturing facility.
• In depth awareness of entire process; identifying operational factors which influence the process.
• A competent Reviewer and Approver of SOPs, protocols, reports or records.
• Can trouble‑shoot and weigh up all information to choose the optimum path.
• Demonstrate ability to lead a small project and manage the deliverables effectively.

Skills

Quality Assurance

cGMP

Data Integrity

Deviation Management

CAPA

Auditing

Education

Bachelor's Degree in Life Sciences

Job description

No deviation Pte Ltd. in Singapore seeks a QA Senior Specialist to advance day-to-day quality assurance activities across cGxP contract manufacturing.

You will review SOPs, participate in deviations, CAPA, audits, and change controls, ensuring data integrity and compliance with regulatory standards. Responsibilities span QA validation, technical compliance, and cross-functional collaboration with QC, Engineering, and Validation teams to release products on time while maintaining the highest