factory manager

Get Spirit; Bontomarannu; On-site; IDR 900,000,000 - 1,500,000,000; Full time

Job summary

Get Spirit is seeking a Factory Manager to lead end-to-end pharmaceutical and health supplement manufacturing operations, from procurement to distribution.

The role requires overseeing Production, QA, QC, and Regulatory Affairs, ensuring GMP/CPOB compliance and quality systems.

You will build capabilities, drive continuous improvement, and coordinate with multiple functions while maintaining BPOM standards.

Qualifications

• Minimum S1 degree in Pharmacy and completed Pharmacist Professional Education.
• Professional competency in the pharmaceutical industry.
• At least 5 years of work experience in pharmaceutical manufacturing, preferably in managerial roles.
• Experience with GMP/CPOB and regulatory compliance.

Responsibilities

• Lead pharmaceutical manufacturing operations across Production, QA, QC, and Regulatory Affairs.
• Oversee production planning, capacity optimization, productivity, and cost efficiency.
• Ensure GMP/CPOB compliance and regulatory standards are met.
• Develop and audit Quality Management Systems, SOPs and quality documentation; conduct audits.
• Manage QA/QC processes including raw materials, in-process inspections, and finished product testing; validate methods.
• Handle RCA and CAPA for quality issues and non-conformances.
• Coordinate across Production, QA, QC, PPIC, Warehouse, Procurement, and Regulatory Affairs.
• oversee product registration, licensing, and BPOM regulatory compliance.
• Lead cross-departmental teams and drive continuous improvement.

Skills

Leadership

Quality Assurance

Quality Control

GMP

Regulatory Affairs

Strategic Planning

Education

S1 Pharmacy

Pharmacist Professional Education

Job description

Factory Manager / Plant Manager for a pharmaceutical and health supplement manufacturing company. The role involves leading and managing end-to-end pharmaceutical manufacturing operations, from raw material procurement, production processes, quality oversight, to finished product distribution.

Key responsibilities

Lead and manage pharmaceutical manufacturing operations across multiple functional areas including Production, Quality Assurance (QA), Quality Control (QC), and Regulatory Affairs (RA)

Oversee production planning and control, factory capacity optimization, productivity, cost efficiency, and operational resource management

Implement and maintain compliance with CPOB (Cara Pembuatan Obat yang Baik) / Good Manufacturing Practice (GMP) and pharmaceutical industry quality standards and regulatory requirements

Develop, implement, and evaluate Quality Management Systems, SOPs, quality documentation, and conduct internal and external audit processes

Manage quality assurance and quality control processes including raw material quality control, in-process inspections, finished product testing, and method and process validation

Handle quality non-conformances, conduct Root Cause Analysis (RCA), and implement Corrective and Preventive Actions (CAPA)

Coordinate across departments including Production, QA, QC, PPIC, Warehouse, Procurement, and Regulatory Affairs

Manage product registration processes, licensing, compliance audits, and BPOM regulations

Lead cross-departmental teams, develop employee competencies, and implement continuous improvement programs

Demonstrate strong leadership, strategic planning, analytical thinking, decision-making, and problem-solving capabilities

About you

Minimum S1 degree in Pharmacy with completed Pharmacist Professional Education and professional competency in pharmaceutical industry

Minimum 5 years of work experience in pharmaceutical manufacturing industry with experience in Factory Manager, Plant Manager, Manufacturing Manager, or similar managerial positions

Extensive professional experience managing multiple pharmaceutical factory operational functions, particularly Production, QA, QC, and Regulatory Affairs

Proficiency in applying CPOB / GMP and pharmaceutical industry quality standards and regulatory compliance

Experience developing, implementing, and evaluating Quality Management Systems, SOPs, quality documentation, and audit processes

Understanding of Quality Assurance and Quality Control processes including raw material control, in-process production inspections, finished product testing, and method and process validation

Experience handling quality non-conformances, conducting Root Cause Analysis (RCA), and implementing Corrective and Preventive Actions (CAPA)

Capability in production planning and control, factory capacity optimization, productivity, cost efficiency, and operational resource management

Understanding of cross-departmental coordination, particularly Production, QA, QC, PPIC, Warehouse, Procurement, and Regulatory Affairs

Knowledge of product registration processes, licensing, compliance audits, and BPOM regulations