Quality Control Officer (East, 5 days, office hours, no OT) #HAC

Roles & Responsibilities

We are seeking a candidate to conduct quality control checks on incoming materials, in-process products, and finished goods to ensure compliance with quality standards in a GMP-regulated environment.

Job Description:

• Conduct incoming sampling and quality control checks for raw and packaging materials.
• Review incoming documents to ensure compliance with material release specifications.
• Prepare samples and perform odour testing
• Perform in-process quality control checks on work-in-progress and finished products.
• Collect samples for laboratory analysis, retention, and stability testing.
• Record, review, and maintain batch process records.
• Print and manage quality control labels.
• Follow up on quality issues, deviations, investigations, and CAPA for all QC operations.
• Conduct environmental monitoring activities, including air sampling.
• Verify and maintain measurement equipment such as weighing scales and data loggers.
• Coordinate external calibration of measurement equipment.
• Maintain QC data, records, and documentation to ensure traceability and audit readiness.
• Support machine testing, trial runs, equipment qualification, and validation activities.
• Assist in audits, complaint investigations, and other quality assurance activities.

Job Requirement:

• Diploma in Pharmaceutical Science, Chemical Science, or a related discipline.
• Working knowledge of cGMP and ISO requirements.
• Meticulous, organised, and able to manage multiple priorities in a GMP manufacturing environment.
• Strong interpersonal and communication skills, with the ability to work effectively with employees at all levels.
• Good analytical and problem-solving skills.
• Able to work independently as well as collaboratively in a team environment.

Interested candidates please send your resume to anna.chen@recruitexpress.com.sg

Anna Chen jiaxin
CEI No: R25157621
Recruit Express Pte Ltd
EA License: 99C4599

Tell employers what skills you have

CAPA
Deviations
Cleanliness Testing
Laboratory Data Analysis
CGMP practices
Investigation
Quality Checking
Priority Management
Pharmaceutical Sciences
Interaction with employees
Analytical and Problem-Solving Skills
Packaging Testing
compliance documentation
Collaborate With Internal Team
Batch Management
Able To Work Independently