Validation Jr Manager

PT Pyridam Farma Tbk; Desa Ciranjeng; On-site; IDR 260,000,000 - 420,000,000; Full time

Job summary

PT Pyridam Farma Tbk is seeking a Junior Manager – Validation to lead and oversee validation activities ensuring GMP/CPOB compliance and quality standards. You will provide leadership across CSV, process validation, cleaning validation, and qualification programs, while supporting GMP audits and CAPA follow-up.

The role focuses on developing the validation team and improving capabilities, with willingness to be based in Cikarang.

Qualifications

• Licensed Pharmacist (Apoteker) required.
• 7+ years of validation experience in pharma or 2+ years as Validation Supervisor.

Responsibilities

• Lead validation activities across CSV, process validation, cleaning validation, and qualification of equipment and facilities.
• Support GMP audits, CAPA follow-up, and continuous improvement initiatives.

Skills

Licensed Pharmacist

7+ years Validation experience

GMP/CPOB knowledge

CSV expertise

Audit and CAPA experience

Leadership and people management

Strong analytical skills

Detail-oriented

Tools

CSV (Computerized System Validation)

Process Validation

Job description

Hi Pharmacist!
We are looking for a Junior Manager – Validation who will be responsible for leading and overseeing validation activities to ensure compliance with GMP/CPOB, applicable pharmaceutical regulations, and company quality standards.

The position will provide leadership and technical direction across validation activities, including Computerized System Validation (CSV), Process Validation, Cleaning Validation, Equipment & Facility Qualification, and other applicable validation programs. The role will also support GMP audits, CAPA follow-up, and continuous improvement initiatives while developing the capability and performance of the validation team.

• Must be a Licensed Pharmacist (Apoteker)
• Minimum 7 years of experience in Validation within the pharmaceutical industry, or minimum 2 years of experience as Validation Supervisor
• Strong knowledge and hands-on experience in Good Manufacturing Practices (GMP/CPOB) and applicable pharmaceutical regulations.
• Experienced in GMP audits, including audit preparation, participation, response to audit findings, and CAPA follow-up.
• Proven experience in Computerized System Validation (CSV), including validation planning, risk assessment, documentation, and execution.
• Good understanding of process validation, cleaning validation, equipment/facility qualification, and other applicable validation activities.
• Strong leadership and people management skills, including coaching, delegation, performance evaluation, and competency development.
• Strong analytical, problem-solving, communication, and coordination skills.
• Detail-oriented, organized, and committed to quality, compliance, and continuous improvement.
• Willing to be based in Cikarang.

Pharmaceuticals, Biotechnology & Medical Devices 101-1,000 employees

Start in 1976 Pyridam established with small factory. In 1985, Pyridam established its Pharmaceutical Division, which develop quickly. Pyridam was awarded the title “Partner with Good Performance” in 1994 by the Ministry of Agriculture and Accelerated improvement enabled Pyridam to build a brand new production plant on 35,000 sqm land in Cianjur, West Java, with state of the art design, machinery, and environmental management. The plant started its operation in April 2001.

We manufacture a wide range of products from modern and traditional medicine i.e., Antibiotics, Vitamins, Supplements, and Traditional herbal care.

The products have met the GMP - Good Manufacturing Process Standard

Start in 1976 Pyridam established with small factory. In 1985, Pyridam established its Pharmaceutical Division, which develop quickly. Pyridam was awarded the title “Partner with Good Performance” in 1994 by the Ministry of Agriculture and Accelerated improvement enabled Pyridam to build a brand new production plant on 35,000 sqm land in Cianjur, West Java, with state of the art design, machinery, and environmental management. The plant started its operation in April 2001.

We manufacture a wide range of products from modern and traditional medicine i.e., Antibiotics, Vitamins, Supplements, and Traditional herbal care.

The products have met the GMP - Good Manufacturing Process Standard