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Assistant Manager Formulasi R&D

Job in 51137, Depok, Indonesia
Listing for: PT Mersifarma TM
Full Time position
Listed on 2026-05-30
Job specializations:
  • Pharmaceutical
    Pharmaceutical Manufacturing
  • Research/Development
Job Description & How to Apply Below
  • Manage and supervise formulation development activities for new pharmaceutical products as well as existing product improvements in accordance with company targets.
  • Coordinate formulation trials, scale-up processes, technology transfer, and process validation until products are ready for commercial production.
  • Ensure all research and development activities comply with GMP, GLP, CPOB standards, and applicable BPOM regulations.
  • Evaluate raw materials, excipients, formulation methods, and development processes to produce effective, stable, safe, and cost-efficient products.
  • Prepare and review product development documents such as trial protocols, formulation development reports, stability reports, master formulas, and registration documents.
  • Collaborate with QA, QC, Regulatory Affairs, Production, Purchasing, and Marketing departments to support product development activities.
  • Identify and resolve technical issues arising during formulation development, scale-up, and initial production processes.
  • Monitor stability studies and retained sample activities to ensure product quality remains within specifications.
  • Lead, supervise, and develop the formulation team to ensure effective and productive operations.
  • Ensure product development timelines and project targets are achieved according to the approved plan and budget.
  • Prepare periodic reports regarding project progress and R&D activities for management review.
Job Qualifications:
  • Bachelor’s Degree in Pharmacy with Pharmacist Professional Certification (Apothecary).
  • Minimum 4–6 years of experience in Formulation Development Supervisor within the pharmaceutical industry.
  • Experience in leading teams or product development projects is an advantage.
  • Strong understanding of pharmaceutical formulation development, scale-up, technology transfer, and process validation.
  • Good knowledge of GMP, GLP, CPOB, and BPOM regulatory requirements.
  • Strong analytical thinking, problem-solving, and decision-making skills.
  • Good leadership, communication, and cross-functional coordination skills.
  • Able to work in a detailed, systematic, and target-oriented manner.
  • Capable of preparing technical documents and product development reports.
  • Proficient in Microsoft Office and capable of handling research/development data analysis.
  • Good english proficiency, especially for reading technical documents and scientific journals.
  • Willing to work under tight timelines and dynamic product development environments.
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