Lead, Formulation Development & Tech Transfer

Duopharma Biotech; Klang City; On-site; MYR 180,000 - 240,000; Full time

Job summary

Duopharma (M) Sdn. Bhd. in Klang, Selangor, invites an experienced Assistant Manager, Formulation Development (Business Improvement) to lead product quality improvement initiatives and manufacturing process optimisation within a GMP environment.

You will manage formulation trials, evaluate raw materials, support technology transfer from R&D to manufacturing sites, and collaborate with QA, Regulatory, and Production to ensure compliant, timely implementations across multiple projects.

Qualifications

• Bachelor's degree in life sciences or chemistry.
• Master's degree in pharmaceutical sciences or chemistry is a plus.
• Registered Chemist (IKM) or Pharmacist with Pharmacy Board Malaysia preferred.

Responsibilities

• Lead formulation trials and product quality improvement projects.
• Evaluate alternative and new raw materials for manufacturing suitability.
• Review trial results and provide recommendations for continuous improvement.
• Coordinate pilot batch manufacturing and technology transfer from R&D to manufacturing sites.
• Prepare and review technical documents for regulatory and QA stakeholders.
• Ensure QMS and GMP compliance across projects.
• Oversee laboratory equipment maintenance and calibration.
• Lead procurement of laboratory equipment and consumables.

Skills

GMP knowledge

Technical writing

Project management

Cross-functional teamwork

Education

Bachelor's degree in Life Sciences, Pharmaceutical Sciences, Pharmacy, Chemistry, or related discipline

Master's degree in Pharmaceutical Sciences or Chemistry

Job description

Duopharma (M) Sdn. Bhd. in Klang, Selangor, invites an experienced Assistant Manager, Formulation Development (Business Improvement) to lead product quality improvement initiatives and manufacturing process optimisation within a GMP environment.

You will manage formulation trials, evaluate raw materials, support technology transfer from R&D to manufacturing sites, and collaborate with QA, Regulatory, and Production to ensure compliant, timely implementations across multiple projects.