Monitor and supervise production process to ensure compliance with SOP and cGMP. Maintain documentation as per regulatory authorities requirement like change control, deviations. Highlight technical problems and take corrective actions.
interface with the Amgen Global, Site, Biosimilars, and/or Device RA CMC teams for specific strategies or activities that impact a product. Lead submission for annual reports, facility registrations, facility renewals, and product renewals. Interact with authors, reviewers and subject matter experts with respect to delivery of CMC documents required for regulatory submissions.
1 to 3 Years of experience in Production Department of Pharma Formulation. HOF Pharmaceuticals Ltd are a pharmaceutical formulation manufacturing company that is committed to shine through its quality products and exceptional customer service.
Accuprec Research Labs Pvt Ltd. is FDCA approved, OECD-GLP, NABL accredited and ISO 9001:2015 certified CRO. Head Quarter of the CRO is located at Ahmedabad and branch offices at Canada and USA.
Syngene is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.
Manage R&D development related research for specific Drug Delivery Systems to ensure on-time, within budget quality delivery along with a continuous focus on improvements. The candidate will be responsible for conducting hypothesis testing, designing and developing novel formulations using various materials for diverse applications, including development of Liposomal formulations, Nano- and submicron particulate formulations, Polymeric-Based Formulations, etc.
Granules India is a vertically integrated, high-growth pharmaceutical company with 38 years of proven performance and increasing performance and increasing presence across the world. Headquartered in Hyderabad, India, Granules offers collaborative and strategic partnership to global pharmaceutical leaders by producing best quality API, PFI and FD through manufacturing excellence, process innovation and regulatory expertise.
WALK-IN INTERVIEW Production & Quality (OSD Formulations)
Ability to understand and interpret complex and detailed drug, press release-related information from source material. Ability to research and synthesize scientific information
B.Pharm/M.Pharm/D.Pharma; Having relevant experience to operate and maintenance of Compression Granulation, Coating m/c. Documentation QMS for Manufacturing Dept. experience in operation and supervision of CAM/ IMA/Blister/ CVC/ Cartonator/ Documentation QMS for Packing Dept.