Senior QA Engineer (Workplace : Tuas)

CCL DESIGN (SINGAPORE) PTE. LTD.; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

CCL DESIGN (SINGAPORE) PTE. LTD. is seeking a Quality Control professional to coordinate QC activities across production, packaging, and shipment, and to review and approve customer specifications.

The role requires at least a Diploma and 2 years of experience in manufacturing, preferably with exposure to healthcare. Experience with ISO and GMP training, calibration programs, and QA documentation is a plus.

Qualifications

• At least Diploma with 2 years of experience.
• Minimum 2 years in manufacturing, healthcare sector.
• Experience with mechanical test equipment and knowledge of chemical tests is an advantage.

Responsibilities

• Coordinate quality control across production, packing, and shipment.
• Review and approve customer specifications.
• Handle customer, supplier, and internal audits.
• Handle customer feedback and corrective action reports.
• Update weekly, monthly and annual quality performance reports.
• Conduct ISO and GMP training for new employees and refresh training for current employees.
• Create SOPs and maintain controlled documentation.
• Manage customer specifications database.
• Manage calibration program.
• Maintain technical data sheet and Safety data sheet databases.
• Correspond with customers regarding certificates of compliance/analysis.
• Review and filing raw materials certificates of analysis.
• Review and approving batch records prior to production.
• Develop and maintain ISO standards for operations.
• Maintain QA records, inspection reports, and quality metrics; present findings in management reviews.
• Train operators and QA staff on inspection techniques, quality standards, and process improvements.
• Perform other job function at Plant Manager request.

Skills

Microsoft Office

English proficiency

Self-driven

Stress management

Education

Diploma

Job description

Qualification/Competency Criteria

At least Diploma. 2 years working experience

At least 2 years in manufacturing industry, healthcare sector.

Experience in mechanical test equipment and knowledge in chemical test will be an advantage.

Job Description & Requirements

• Coordinate all Quality Control activities across production, packing, and shipment.
• Receiving, reviewing, and approving customer specifications.
• Handle customer audit, supplier audit and internal audit.
• Handle customer feedback and CAR report.
• Update Quality report – Weekly, Monthly and Annual quality performance review report.
• Conduct ISO and GMP training for new employees and refresh training for current employees.
• Create SOP and maintain company control documentation.
• Manage customer specification database.
• Manage calibration program.
• Manage Technical data sheet and Safety data sheet database.
• Corresponds with customers regarding certificates of compliance/analysis.
• Review and filing raw materials certificates of analysis.
• Review and approving batch records prior to production.
• Develop and maintain quality systems: Implement and monitor ISO standards for operations.
• Maintain QA records, inspection reports, and quality metrics; present findings in management reviews.
• Train operators and QA staff on inspection techniques, quality standards, and process improvements.
• Perform other job function at Plant Manager request.

Required skill and competency:

1. Proficient in Microsoft Office Excel, Word and Powerpoint applications
2. Bilingual but good proficiency in English - Spoken & Written
3. Hands-on & self-driven personality requiring minimum supervision
4. Able to handle and manage stressful situations