Pharmaceutical Production(Drug Substance) manager

PT SKPLASMA CORE INDONESIA; Jawa Barat; On-site; IDR 300.000.000 - 500.000.000; Full time

Job summary

A leading biopharmaceutical company in Indonesia is seeking a Pharmaceutical Production Manager to oversee plasma fractionation and protein purification processes. The ideal candidate will have over 10 years of experience in the pharmaceutical industry and a Bachelor's degree in Pharmacy or related fields. Responsibilities include managing operations in compliance with GMP standards and ensuring efficient production of Active Pharmaceutical Ingredients (APIs). Fluency in English is required, with proficiency in Korean preferred.

Qualifications

• 10 years of experience in managing DS processes in pharma.
• Pharmacist License (STRA) required.
• Experience in protein purification processes preferred.

Responsibilities

• Manage overall Plasma fractionation and protein purification.
• Handle API production in biopharmaceutical manufacturing.
• Ensure compliance with GMP standards during operations.

Skills

Pharmaceutical production management

Protein purification

GMP compliance

Chromatography

Fluency in English

Education

Bachelor’s Degree in Pharmacy or equivalent fields

Job description

Pharmaceutical Production (Drug Substance) Manager

SK Plasma has grown steadily on the foundation of PDMP (plasma-derived medicinal products) business starting from 1970. In 2015, SK Plasma resolved to build a state-of-the-art plasma fractionation plant and has spun off from SK Chemicals Life Science biz., aiming to improve competitiveness in the global PDMP market. SK Plasma is building a plasma fractionation plant in order to improve the self-sufficiency of PDMP in Indonesia through a joint venture with capable business partners under the support of the Indonesian government.

Role Description:

• Establishment and management of overall Plasma fractionation and protein purification
• API (Active Pharmaceutical Ingredient) production in biopharmaceutical manufacturing
• Operation and management of chromatography and ultrafiltration/diafiltration process for protein purification
• Operation and management of large-scale reactors, filtration systems, and continuous centrifuges
• Operation and management of sterile filtration procedures in compliance with GMP standards

Required:

• Bachelor’s Degree in Pharmacy or equivalent fields (Biology, Chemistry, etc.)
• Minimum 10 years working experience in performing, managing, and manufacturing DS processes within the pharmaceutical industry
• Having Pharmacist License (STRA)
• Proficiency in English (both written and spoken)

Preferably:

• Experience in fractionation & protein purification processes within the biopharmaceutical industry
• Experience in the initial setup of fractionation & purification processes in a newly constructed biopharmaceutical facility
• Proficiency in Korean (both written and spoken)