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QA Executive

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AI-generated summary

  • Collect and analyze PQR and verification data; prepare reports, maintain QA docs/equipment and perform GMP spot-checks.
  • Work in a Quest3+-based GMP/ISO/Halal quality system.
  • Lead internal GMP/ISO/Halal audits and own QA systems, shaping quality!

RM 2300 - RM 2600

No.69 Jalan TPP 1/13, Taman Perindustrian, Puchong, Selangor

Job Description

 Job description: 

  1. Collecting data for the Product Quality Review (PQR).
  2. Compile, analyze and prepare PQR report.
  3. Prepare verification protocols and monitor the verification process.
  4. Compile and analyze verification data and results.
  5. Prepare the final verification report.
  6. Ensure proper arrangement of equipment handled by the QA department.
  7. Order new or replacement equipment as necessary and update the master list of equipment.
  8. Prepare Quality Procedures (QP), Work Instructions (WI) and FORM for the QA Department.
  9. Ensure that QP/WI/FORM are updated and distributed according to procedures.
  10. Ensure that change control documents and obsolete documents are managed in accordance with procedures.
  11. Ensure that pest control agreements are available and up to date.
  12. Ensure that the Safety Data Sheets (SDS) are updated.
  13. Ensure that the layout is updated as required.
  14. Ensure that the master list for chemical cleaning is available and updated.
  15. Ensure that preventive maintenance for dispensers is followed according to schedule and documented.
  16. Update the master list of calibrated equipment.
  17. Update the master list of calibrated equipment.
  18. Ensure that external calibrations are performed according to schedule and that certificates are filed in accordance with procedures.
  19. Verify the write-off of items during the disposal process.
  20. Coordinate with the warehouse to arrange disposal through Kualiti Alam.
  21. Review and update the BMR to ensure that the BMR is consistent with Quest3+
  22. Complete the variation form if there is a discrepancy between the BMF or product specifications and Quest3+.
  23. To issue Sample Requisition Form for every batch manufacturing/repacking.
  24. Conduct GMP spot-checks as required.
  25. Perform personal hygiene checks in accordance with established standards.
  26. Serve as an internal auditor for GMP/ISO and Halal audits.
  27. Undertake any other duties as directed by the superior from time to time.

Job Requirements

Requirement:

  1. Minimum Diploma in relevant field.
  2. Preferably at least 1-2 years of working experience in Quality Control & Quality Assurance in a manufacturing environment.

Skills

Microsoft Word
Material Safety Data Sheet
Document Control
Multitasking

Company Benefits

Panel clinics with medical benefits

Provides comprehensive healthcare coverage to ensure the well-being of employees

Performance Bonuses

Financial incentives based on individual and company performance to reward your hard work.

Competitive Compensation

Ensures employees are fairly compensated for their contributions.

Convenient location

Near to LRT station

Training & Personal Development

Offers employees opportunities for continuous learning and career advancement.

Employee Assistance Program

Provides confidential support for personal and professional challenges, including counseling services.


Additional Info

Company Activity

Last active - few minutes ago

Career Level

Junior Executive

Job Specialisation


Company Profile

Esprit Care Sdn Bhd-logo-image

Esprit Care Sdn Bhd

Our company prides itself on its state-of-the-art highly automated, GMP-certified facilities, which allow us to produce a wide array of dosage forms, including capsules, tablets, softgels, probiotics, powder sachets, and liquid formulations. Leveraging our in-house R&D expertise, we collaborate closely with ingredient suppliers clients to develop tailored products that meet market demands and regulatory standards...