We are hiring for Production Assistant Manager & Executive to work with our manufacturing operations, ensuring consistent production of high-quality branded generics across our diverse portfolio of oral liquids, solids, and topical dosage forms. This is a critical role for our organization, and the ideal candidate will be a strategic leader with a proven track record of driving productivity improvements, operational excellence, optimizing efficiency, and ensuring strict adherence to cGMP compliance. Responsibilities: • Oversee the day-to-day operations of all production departments, including: Oral Liquids Manufacturing Solid Dosage Manufacturing Collaboration with Quality Control, Quality Assurance, Engineering, Warehouse, Production Planning, Marketing, Finance and Research & Development • Manage relationships with key stakeholders, including R&D, Quality Assurance, and Supply Chain teams. • Identify and implement new technologies and processes to improve production efficiency and product quality. • Prepare and present production reports and metrics to leadership team.

We are seeking a skilled and detail-oriented Analytical FR&D Executive to join our Formulation Research & Development team. The ideal candidate will have hands-on experience in analytical method development, validation, and routine analysis supporting formulation projects. This is a critical role that ensures product quality, compliance, and supports regulatory filings for both domestic and international markets. Key Responsibilities: Conduct analytical method development and validation for finished pharmaceutical dosage forms (solid, liquid, semi-solid) Perform routine analysis of stability and development samples as per ICH guidelines Prepare and review analytical documentation , including method validation protocols, SOPs, and reports Support formulation teams by providing timely and accurate analytical data Handle instruments such as HPLC, UV-Vis Spectrophotometer, FTIR, Dissolution Tester, GC, etc. Ensure adherence to GLP , GMP , and data integrity practices in the laboratory Coordinate with cross-functional teams including formulation, QA, and RA during product development and scale-up Support in compiling data for regulatory submissions (ANDA, CTD, Dossier, etc.)

Position: Production Executive / Officer Injectables Location: Ankleshwar,Gujarat Experience: 2-4 years Key Responsibilities: Carry out production activities as per SOPs and schedule Ensure adherence to cGMP and regulatory guidelines Maintain accurate production documentation (BMRs, logbooks) Coordinate with QA/QC for line clearance and sampling Support equipment cleaning, operation, and minor troubleshooting Follow all safety and hygiene protocols Requirements: B.Pharm/M.Pharm/B.sc/ Msc or equivalent 2- 4years experience in parental production Good knowledge of GMP and pharma documentation Strong attention to detail and communication skills

Job Description: Regulatory Affairs Assistant Manager / Manager Injectable & OSD Facility Department: Regulatory Affairs Location: GIDC Ankleshwar Key Responsibilities: Prepare and submit dossiers (CTD/ACTD) for ROW & US markets. Ensure compliance with local regulatory guidelines and GMP standards. Liaise with regulatory agencies and respond to queries promptly. Manage product registrations, renewals, and variations. Monitor regulatory updates and ensure adherence to changes. Support quality audits and review labeling/artwork for compliance .