Chemist

Sunward Pharmaceutical; Johor Bahru; On-site; MYR 72,000 - 96,000; Full time

Job summary

Sunward Pharmaceutical is seeking a QC supervisor to manage routine QC testing for materials and finished products in Johor Bahru. The role requires ensuring GMP/GLP/GDP compliance and reviewing QC documentation and BMR records.

The candidate will supervise and train lab technicians, support investigations, and collaborate with Production, QA, and R&D on quality issues. A relevant degree and at least 2 years of experience are welcomed.

Qualifications

• Bachelor's degree or Diploma in Pharmacy, Chemistry or equivalent is required.
• Minimum 2 years of relevant QC/Lab experience is welcomed.

Responsibilities

• Manage and supervise routine QC testing for raw materials, packaging materials, semi-finished, and finished products.
• Ensure compliance with GMP, GLP, GDP, SOPs, POA, and product specifications.
• Review QC documentation, analytical reports, logbooks, and BMR records.
• Supervise and train lab technicians on routine laboratory operations and testing procedures.
• Support routine laboratory testing when required.
• Maintain laboratory cleanliness, equipment calibration, and sample records.
• Supervise preparation, labelling, storage, and disposal of reagents, chemicals, and samples.
• Support investigations, product complaints, root cause analysis, and CAPA activities.
• Collaborate with Production, QA, and R&D departments on quality-related matters.
• Assist in updating SOPs, specifications, and QC-related documents.
• Manage routine QC laboratory operations in the absence of the QC HOD.

Education

Bachelor's degree / Diploma in Pharmacy or Chemistry / equivalent

Job description

Jora Malaysia will close on 9th September 2026. Thank you for being with us, we are cheering you on as you continue your career journey.

Manage and supervise routine QC testing for raw materials, packaging materials, semi-finished, and finished products.

Ensure compliance with GMP, GLP, GDP, SOPs, POA, and product specifications.

Review QC documentation, analytical reports, logbooks, and BMR records.

Supervise and train lab technicians on routine laboratory operations and testing procedures.

Support routine laboratory testing when required.

Maintain laboratory cleanliness, equipment calibration, and sample records.

Supervise preparation, labelling, storage, and disposal of reagents, chemicals, and samples.

Support investigations, product complaints, root cause analysis, and CAPA activities.

Collaborate with Production, QA, and R&D departments on quality-related matters.

Assist in updating SOPs, specifications, and QC-related documents.

Manage routine QC laboratory operations in the absence of the QC HOD.

Requirements:

Candidates must possess at least Bachelor's degree/ Diploma Degree in Pharmacy/ Chemistry/ equivalent.

Qualified candidates with at least 2 year of working experience in relevant field are welcomed to apply.