# Elevate Your Pharmaceutical Career: Join PT Novell Pharmaceutical Laboratories
Established in 1998, PT Novell Pharmaceutical Laboratories has solidified its position as a cornerstone of the healthcare manufacturing industry. Operating under the highest international standards, the company is synonymous with excellence in Good Manufacturing Practice (GMP). A major milestone in the firm's history occurred in 2013, when it became the first Indonesian pharmaceutical company to receive GMP approval from the European Union (Germany – Lageso) for its injection production facility.
Today, Novell Pharmaceutical Laboratories stands as a premier industry leader, holding a rare collection of GMP certifications from Europe, Australia, the South African PICS, and the Gulf Cooperation Council (GCC) nations. Driven by an aggressive international growth strategy, the company maintains a robust physical presence in the Philippines, Thailand, and Vietnam, supported by a dedicated team of over 30 international professionals.
As we continue to innovate and expand our pharmaceutical footprint, we are inviting high-caliber professionals to join our team in September 2026. This is an exceptional opportunity to advance your career with an organization that values quality, precision, and global standards.
## Current Career Opportunities
We are currently seeking talented individuals to fill the following roles at our Gunung Putri facility in Bogor:
1. Staff Analytical Development (Data Processing)
2. Staff Quality Control (Data Processing)
## Candidate Qualifications
To thrive in these critical roles, applicants should possess the following expertise and background:
* Educational Background: Hold a Bachelor’s degree (S1) in Chemistry or Pharmacy.
* Experience: Previous experience in Research & Development (R&D) or Analytical Development is essential for the AD position.
* Compliance Knowledge: A comprehensive understanding of CPOB and GMP guidelines is mandatory, alongside a strong sense of discipline, responsibility, and meticulous attention to detail.
* Technical Proficiency: Proven experience working in a laboratory setting, with hands-on capability in operating analytical instrumentation, including HPLC, GC, and UV-Vis Spectrophotometers.
* Soft Skills: Strong interpersonal and communication skills to collaborate effectively within a team environment.
* Availability: Must be willing to work within a shifting or off-shift schedule as required by production demands.
## How to Apply
If you are ready to contribute to a world-class pharmaceutical manufacturing team, we encourage you to submit your updated curriculum vitae to our recruitment office.
* Email Address: [email protected]
* Subject Line Requirements: Please ensure your email subject matches the specific role:
* For Analytical Development: `Link_Staff AD Lokal`
* For Quality Control: `Link_Staff QC`
Take the next step in your professional journey and join a company that bridges local expertise with international standards. We look forward to reviewing your application and exploring how your skills can support our mission of delivering high-quality healthcare solutions.