Formulation Lead — Product Transfer & Process Improvement

Medela Potentia; Bogor; On-site; IDR 89,280,000 - 156,240,000; Full time

Job summary

Medela Potentia in Bogor, Indonesia, seeks a Formulation Officer to lead product transfer projects, optimize formulations, and ensure GMP compliance for commercial products. You will design manufacturing recipes, support validation, and prepare technical documentation.

Ideal candidates have a Bachelor’s in Pharmacy, Pharmacist registration preferred, and 2–3 years in production or technical service within pharma, with strong English and Indonesian proficiency.

Qualifications

• Bachelor’s Degree (S1) in Pharmacy; Registered Pharmacist preferred.
• 2–3 years in Production, Technical Projects, or Technical Service in the pharmaceutical industry.
• Knowledge of GMP (CPOB/CPOBAB), GDP, formulation development, manufacturing process design, data integrity, and risk management.
• Proficient in Indonesian and English, written and spoken.

Responsibilities

• Plan, execute, and monitor product transfer with focus on technical aspects and timelines.
• Provide hands-on technical support for commercial products, including validation recipes.
• Prepare comprehensive technical documentation, manufacturing instructions, and trial evaluation reports.
• Oversee formulation trials, evaluate material requirements, and optimize formulations and processes.
• Coordinate with internal stakeholders (Production, TS, Quality, Engineering, EHS) for project execution.
• Participate in audits, CAPA, risk management, and process improvements.
• Ensure strict EHS compliance during trials to maintain a safe environment.

Skills

Formulation

GMP/CPOB

Project management

Cross-functional

Education

Bachelor's in Pharmacy

Registered Pharmacist

Job description

Medela Potentia in Bogor, Indonesia, seeks a Formulation Officer to lead product transfer projects, optimize formulations, and ensure GMP compliance for commercial products. You will design manufacturing recipes, support validation, and prepare technical documentation.

Ideal candidates have a Bachelor’s in Pharmacy, Pharmacist registration preferred, and 2–3 years in production or technical service within pharma, with strong English and Indonesian proficiency.