Manufacturing Associate

Job Description

Company Description Novala Biotech Pvt Ltd is an in vitro diagnostic (IVD) research and manufacturing company in Nepal, driven by a multidisciplinary team of healthcare and research professionals. The organization focuses on developing high-quality diagnostic kits through evidence-based research to support accurate and timely medical decisions. Novala Biotech collaborates closely with Shikhar Biotech Pvt Ltd to advance molecular biology and create diagnostic solutions tailored to the needs of the local population. The company is committed to maintaining rigorous standards of quality, reliability, and precision while continuously innovating to meet the evolving needs of the healthcare sector. By strengthening national IVD capabilities, Novala Biotech aims to make a lasting impact on healthcare delivery in Nepal.

Role Description The Manufacturing Associate is a full-time, on-site role based in Kathmandu, responsible for supporting the production of IVD kits in a controlled manufacturing environment. Day-to-day tasks include operating and monitoring manufacturing equipment, preparing materials and reagents, and performing routine processes in clean rooms according to established protocols. The role involves following Good Manufacturing Practice (GMP) standards, documenting production activities, and assisting with in-process quality checks to ensure product consistency and compliance. The Manufacturing Associate will collaborate with cross-functional teams, communicate effectively with supervisors and colleagues, and proactively report any deviations or equipment issues. This position contributes directly to the reliable, high-quality manufacturing of diagnostic products used in healthcare settings across Nepal.

Qualifications

• Experience with controlled environments and clean rooms, including adherence to safety and contamination control procedures.
• Knowledge of Good Manufacturing Practice (GMP) and manufacturing operations in a laboratory, pharmaceutical, or biotech setting.
• Understanding of basic quality control principles, including in-process checks, documentation, and compliance with standard operating procedures.
• Strong communication skills for effective coordination with production, quality, and research teams.
• Diploma or bachelor’s degree in biotechnology, microbiology, chemistry, pharmacy, or a related scientific/technical field.
• Ability to follow detailed instructions, maintain accurate records, and work with meticulous attention to detail.
• Comfort with standing for extended periods, handling laboratory materials, and working in a regulated manufacturing environment.
• Prior experience in IVD, pharmaceutical, or medical device manufacturing is an advantage.