Production Pharmacist

AT Isotop Sdn Bhd; Kuala Selangor; On-site; MYR 60,000 - 90,000; Full time

Job summary

AT Isotop Sdn Bhd seeks a dedicated Pharmacist to join our pharmaceutical manufacturing team in Malaysia. The role covers oversight of preparation, production and quality assurance within a GMP cleanroom, ensuring compliance and patient safety.

The successful candidate will apply GMP/GDP knowledge, contribute to batch reviews, documentation and release activities, and support continuous improvement in a regulated environment.

Qualifications

• Bachelor's Degree in Pharmacy required.
• Registered Pharmacist with a valid practicing license (where applicable).
• Experience in radio-pharmaceutical manufacturing, sterile compounding, or cleanroom operations preferred.
• Strong knowledge of GMP, GDP, aseptic processing, and pharmaceutical quality systems.
• Excellent attention to detail and documentation skills.

Responsibilities

• Supervise pharmaceutical manufacturing activities in a cleanroom environment.
• Ensure GMP, GDP, SOPs, and regulatory compliance.
• Perform batch review, documentation, and release activities.
• Monitor environmental conditions and aseptic techniques in the cleanroom.
• Conduct quality checks and investigate deviations or non-conformances.
• Collaborate with Production, QA, and QC for efficient manufacturing.
• Participate in equipment qualification, process validation, and continuous improvement.
• Train and mentor production personnel on GMP and cleanroom practices.
• Ensure accurate inventory control and proper handling of materials.

Skills

Pharmaceutical knowledge

GMP/GDP knowledge

Cleanroom operations

Documentation

Teamwork

Communication

Education

Bachelor's Degree in Pharmacy

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.

We are seeking a dedicated and detail-oriented Pharmacist to join our pharmaceutical manufacturing team. In this role, you will oversee and support the preparation, production and/or quality assurance of pharmaceutical products within a GMP-compliant cleanroom environment. The successful candidate will ensure compliance with regulatory standards while maintaining the highest levels of product quality and patient safety.

Key Responsibilities

• Supervise pharmaceutical manufacturing activities in a cleanroom environment.
• Ensure compliance with Good Manufacturing Practice (GMP), Standard Operating Procedures (SOPs), and regulatory requirements.
• Perform batch review, documentation, and release activities.
• Monitor environmental conditions and aseptic techniques to maintain cleanroom standards.
• Conduct quality checks and investigate deviations or non-conformances.
• Collaborate with Production and/or Quality Assurance, and Quality Control teams to ensure efficient manufacturing processes.
• Participate in equipment qualification, process validation, and continuous improvement initiatives.
• Train and mentor production personnel on GMP and cleanroom practices.
• Ensure accurate inventory control and proper handling of raw materials and finished products.

Requirements

• Bachelor's Degree in Pharmacy.
• Registered Pharmacist with a valid practicing license (where applicable).
• Experience in radio-pharmaceutical manufacturing, sterile compounding, or cleanroom operations is preferred.
• Strong knowledge of GMP, GDP, aseptic processing, and pharmaceutical quality systems.
• Excellent attention to detail and documentation skills.
• Ability to work in a controlled cleanroom environment while following strict gowning and contamination control procedures.
• Strong communication, teamwork, and problem-solving skills.