Introduction
We are seeking a dedicated Pharmacist – Manufacturing Specialist to join our dynamic team at our state‑of‑the‑art facility in Majalengka. This full‑time position offers a stimulating environment where pharmaceutical manufacturing excellence meets rigorous quality standards. The ideal candidate will bring at least three years of hands‑on experience in the pharmaceutical sector, a solid educational foundation (minimum S1), and a passion for ensuring that every batch produced meets the highest safety, efficacy, and regulatory expectations.
Responsibilities
- Oversee and coordinate all manufacturing activities to guarantee compliance with Good Manufacturing Practices (GMP) and internal quality policies.
- Lead cross‑functional collaboration between Production, Quality Assurance (QA), and Quality Control (QC) teams to maintain product consistency.
- Develop, review, and approve batch records, standard operating procedures (SOPs), and validation protocols.
- Monitor critical process parameters, identify deviations, and implement corrective and preventive actions (CAPA) promptly.
- Conduct risk assessments and trend analyses to proactively address potential quality issues.
- Ensure accurate documentation and traceability for all manufacturing steps, from raw material receipt to final product release.
- Participate in internal and external audits, providing evidence of compliance and addressing auditor findings.
- Mentor junior pharmacists and production staff on GMP principles, safety practices, and continuous‑improvement initiatives.
- Collaborate with R&D and engineering departments to facilitate technology transfers and scale‑up projects.
- Maintain a safe working environment by enforcing occupational health and safety guidelines.
Requirements
- Minimum Bachelor’s degree in Pharmacy (S1) from an accredited university.
- At least 3 years of professional experience in pharmaceutical manufacturing, preferably within a GMP‑regulated environment.
- Demonstrated expertise in Production, QA, or QC functions, with a strong grasp of regulatory frameworks such as FDA, EMA, and local health authority guidelines.
- Excellent analytical and problem‑solving abilities, capable of making data‑driven decisions under pressure.
- Exceptional attention to detail, especially concerning documentation accuracy and batch record integrity.
- Proven ability to work both independently and as an integral member of multidisciplinary teams.
- Strong communication skills, both written and verbal, to effectively liaise with internal stakeholders and external auditors.
- Willingness to be based at the Majalengka site and to work the standard schedule of Monday‑Saturday, 08:00‑17:00.
- All genders are welcomed; the role values diversity and inclusion.
Benefits
- Competitive salary package with performance‑based bonuses.
- Comprehensive health insurance covering medical, dental, and vision care.
- Retirement savings plan with company matching contributions.
- Professional development allowance for certifications, conferences, and advanced training.
- Paid time off, including annual leave, sick leave, and national holidays.
- Employee assistance program (EAP) for personal and family support.
- Transportation allowance or company‑provided shuttle service to the Majalengka site.
- Opportunities for career advancement within a growing pharmaceutical organization.
About Company
Our company is a leading player in the Indonesian pharmaceutical market, dedicated to delivering high‑quality medicines that improve the health and wellbeing of patients nationwide. With a robust portfolio spanning generic, over‑the‑counter, and specialty products, we operate cutting‑edge manufacturing facilities that adhere to the most stringent international standards. We foster a culture of innovation, continuous improvement, and ethical responsibility, encouraging every employee to contribute ideas that drive operational excellence. Join us and become part of a forward‑thinking team that values scientific expertise, teamwork, and a commitment to patient safety.
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