Senior External Manufacturing Quality Lead

PT Taisho Pharmaceutical Indonesia Tbk.; Depok; On-site; IDR 446,400,000 - 781,200,000; Full time

Job summary

Taisho Pharmaceutical Indonesia Tbk. is seeking an External Manufacturing Quality Manager to oversee quality activities for external manufacturing and OEM partners.

The role ensures compliance with product specifications, quality standards, and regulatory requirements throughout the product lifecycle. The ideal candidate has at least 10 years of pharmacist experience in the pharmaceutical industry, with expertise in GMP, process transfer, and packaging development.

Qualifications

• Pharmacist with at least 10 years of experience in the pharmaceutical industry.
• Experience in process transfer and manufacturing technology.
• Experience in product development and packaging development.
• Experience in pharmaceutical processing, technology, and GMP.
• Experience handling other product categories such as food, medical devices, and related categories.
• Strong understanding of GMP and related regulations.
• Excellent communication skills and computer literacy.

Responsibilities

• Oversee quality of products manufactured by external partners to ensure compliance with product specifications and GMP.
• Oversee quality assessments, partner performance, and quality activities throughout the product lifecycle.
• Support Business Development and New Product Development with quality input for toll manufacturing and rebranding.
• Collaborate with internal teams and external manufacturers to execute quality-related activities.
• Establish and monitor quality requirements for external manufacturers.
• Participate in quality risk assessments and oversee site quality aspects.

Skills

Pharmacist

GMP knowledge

Communication skills

Computer literacy

Education

Bachelor of Pharmacy

Job description

Taisho Pharmaceutical Indonesia Tbk. is seeking an External Manufacturing Quality Manager to oversee quality activities for external manufacturing and OEM partners.

The role ensures compliance with product specifications, quality standards, and regulatory requirements throughout the product lifecycle. The ideal candidate has at least 10 years of pharmacist experience in the pharmaceutical industry, with expertise in GMP, process transfer, and packaging development.