# Advance Your Career: Career Opportunities at Novell Pharmaceutical Laboratories
Established in 1998, Novell Pharmaceutical Laboratories stands as a distinguished leader in the pharmaceutical manufacturing sector, operating under the highest national and international Good Manufacturing Practice (GMP) standards. As an industry pioneer, Novell achieved a historic milestone in 2013 by becoming the first Indonesian pharmaceutical company to receive GMP approval from the European Union (Germany – Lageso) for its injection facility.
Today, Novell remains a unique force in the industry, holding prestigious GMP licenses from regulatory bodies in Europe, Australia, South Africa (PICS), and the Gulf Cooperation Council (GCC) nations. Driven by a vision of global reach, the company has successfully expanded its footprint, maintaining dedicated marketing teams and offices across the Philippines, Thailand, and Vietnam, supported by a growing workforce of over 30 international professionals.
## Join Our Dynamic Team in 2026
Novell Pharmaceutical Laboratories is currently inviting passionate and highly motivated professionals to join our expanding team. We are looking for talented individuals eager to grow their careers within a company that prioritizes quality, innovation, and global standards. We are currently accepting applications for the following positions:
1. Staff Analytical Development (Data Processing)
2. Staff Quality Control (Data Processing)
## Candidate Qualifications and Requirements
To ensure we maintain our commitment to excellence, we seek candidates who meet the following professional criteria:
* Educational Background: Minimum Bachelor’s degree (S1) in Chemistry or Pharmacy.
* Professional Experience: Previous experience in Research & Development (R&D) or Analytical Development is essential for the AD staff position.
* Technical Proficiency: Strong understanding of laboratory processes and hands-on experience in a laboratory environment.
* Analytical Instrument Expertise: Proficiency in operating analytical instruments, specifically HPLC, GC, and UV-Vis Spectrophotometers.
* Regulatory Knowledge: Deep understanding and application of CPOB and GMP guidelines.
* Soft Skills: Proven ability to communicate effectively, coupled with high levels of discipline, precision, and personal responsibility.
* Availability: Willingness to work in a shifting schedule format.
## Work Location and Application Process
These positions are based at our primary production facility in Gunung Putri, Bogor.
If you are ready to elevate your career and contribute to a world-class pharmaceutical manufacturer, please submit your updated curriculum vitae (CV) to our recruitment team at:
Email: [email protected]
Email Subject Format: Please ensure your email subject follows this structure for proper processing:
Link_Staff AD Lokal* (For Analytical Development)
Link_Staff QC* (For Quality Control)
Take the next step in your professional journey and join a company that bridges the gap between local expertise and global pharmaceutical excellence.