Introduction
The position of Senior Laboratory Analyst – Product Quality Testing is a critical role within our quality assurance division. The successful candidate will lead laboratory activities that ensure our pharmaceutical and consumer‑health products meet the highest standards of safety, efficacy, and regulatory compliance. Reporting to the Head of Quality Control, the analyst will work closely with cross‑functional teams, including R&D, production, and regulatory affairs, to deliver reliable analytical data that supports product releases and continuous improvement initiatives.
Responsibilities
- Plan, execute, and supervise analytical testing of raw materials, in‑process samples, and finished products using techniques such as HPLC, GC, UV‑Vis, and microbiological assays.
- Develop, validate, and transfer analytical methods in accordance with ICH, USP, and local regulatory guidelines.
- Maintain accurate laboratory notebooks, electronic laboratory information management systems (LIMS), and ensure all data are traceable and auditable.
- Interpret test results, generate comprehensive reports, and communicate findings to production and regulatory teams.
- Provide technical mentorship to junior analysts, conduct on‑the‑job training, and promote a culture of continuous learning.
- Coordinate with equipment vendors for calibration, maintenance, and troubleshooting of critical instrumentation.
- Participate in internal and external audits, addressing non‑conformances and implementing corrective actions promptly.
- Monitor and improve laboratory safety practices, ensuring compliance with OSHA, GMP, and company safety policies.
- Assist in the preparation of regulatory submissions, including stability studies, batch release documentation, and product dossiers.
- Contribute to process optimization projects aimed at reducing turnaround time, cost, and waste while maintaining data integrity.
Requirements
- Minimum education: High School Diploma (SMA/SMK) or equivalent; a degree in Pharmacy, Chemistry, or a related scientific field is highly preferred.
- At least 2–3 years of hands‑on experience in a pharmaceutical or related quality control laboratory.
- Proven competency with standard analytical instrumentation and laboratory software.
- Strong communication skills, both written and verbal, to effectively present technical information.
- Demonstrated honesty, responsibility, and a commitment to ethical laboratory practices.
- Ability to work independently as well as collaboratively within multidisciplinary teams.
- Resilience under pressure; capable of meeting tight deadlines while maintaining accuracy.
- Gender: Open to all candidates; diversity and inclusion are core company values.
- Fluency in Bahasa Indonesia and basic proficiency in English for reading technical documents.
Benefits
- Competitive salary package with performance‑based bonuses.
- Comprehensive health insurance covering medical, dental, and vision.
- Retirement savings plan with company matching contributions.
- Professional development allowance for certifications, workshops, and conferences.
- Paid annual leave, sick leave, and national holidays.
- Employee assistance program and wellness initiatives, including gym membership subsidies.
- Opportunities for career advancement within a fast‑growing organization.
About Company
Our company is a leading manufacturer of high‑quality pharmaceutical and consumer health products, serving both domestic and international markets. With a strong commitment to innovation, regulatory excellence, and sustainable practices, we have built a reputation for delivering safe, effective, and affordable solutions to millions of people. Our state‑of‑the‑art manufacturing facilities are ISO‑9001 and GMP certified, and we invest heavily in research and development to stay ahead of industry trends. Joining our team means becoming part of a dynamic, forward‑thinking environment where your expertise will directly impact product quality and patient safety.
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