Company Jobs

Seeking a highly motivated and results-driven Production In-charge to oversee the manufacturing operations for our range of high-quality DNA/RNA Extraction Kits and Lateral Flow Kits

Strong knowledge of country-specific labeling regulations and guidelines across the US, EU, Canada, Australia, and Switzerland, combined with hands-on experience in label development, including CCDS, USPI, and packaging components. 

Personnel monitoring. Trend analysis and reporting. Sample handling. EM monitoring in aseptic process area including Grade A,B,C and D

The Manager, Regulatory Affairs – CMC is responsible for developing and implementing regulatory strategies related to Chemistry, Manufacturing, and Controls (CMC) for pharmaceutical or biologic products.

Qualification of equipment & Documentation, IPQA, QMS-Ohange Control CAPA, Deviation, Process Validation, Cleaning Validation, APQR, Audit Compliance.

Operation of Blister machines. Troubleshooting, BQS Cartonator: Operation of Cartoning machines. Troubleshooting

Coordination with quality control department & quality assurance department for getting analytical data with respect to , process optimization batches & validation batches.

Look for system / process-focused analysts with RIM / Veeva experience. Excellent communication and stakeholder management skills.

Basic organic chemistry and reaction mechanisms. Literature search and patent search activities.