Exposure in investigation of UPD , OOS, OOT, EM and Change control & CAPA Management. Preferable for exposure in Regulator}’ and FDA Audits, Knowledge and exposure for aseptic operations and principal of its relevant equipment.
2-7 years of experience in production planning, change control, line clearance, deviation handling, autoclave operation TS and component, aseptic and control area operation, documentation, both SVP and LVP manufacturing 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, Warehouse, Engineering & IPQA (OSD Formulations)
Respond to medical information requests from internal and external customers and ensure the responses are medically and scientifically accurate, timely, balanced, and meet customers’ needs.
Lead and enable strong cross-functional partnership between Regulatory Affairs and all key stakeholders including R&D, Product Management, Quality, Clinical Affairs, and other functions at all levels within the business, and the local Regulatory Affairs teams in the Philips market organization.
Supports audit readiness by ensuring files are reviewed according to the schedule detailed in the organization's SOP and department guidance document. Aids the development of the critical path for site activation within assigned projects in support of rapid site activations.
The National Seminar on ADVANCES IN PHARAMCEUTICAL TECHNOLOGY is a platform designed to explore the forefront of pharmaceutical innovation and application. Over two days, this seminar will delve into cutting-edge advancements shaping the future of the industry, offering participants a unique opportunity to gain insights from distinguished experts.
Registered under clause c of Section 31 or Section 32 of the Pharmacy Act 1948. Person serving in similar, equivalent or higher grades in the civil posts in the Defence Services and possessing the following qualifications. Storing medicine, distribution/ issue medicine, maintaining records and making indent.
M.Sc. in Chemistry, Bio-chemistry, Analytical Chemistry or Forensic Science Chemistry or M. Pharma Pharmaceutical Analysis. experience in GC-MS/MS. National Dope Testing Laboratory, an autonomous body, Government of India, is a premier scientific Institute and one of the World Anti-Doping Agency Accredited Laboratories dedicated to human sports dope testing & allied research.
Degree in Pharmacy or Diploma in Pharmacy from a recognized university, institution. Registration with Pharmacy Council under section-12 of Pharmacy Act 1948.
4 Years Degree from any Recognized Board, University in concerned Branches. Maximum age limit 26 years for General Candidate, Relaxable by 03 years in case of OBC, 05 Years in case of SC, ST Candidate.
Applications are invited from eligible candidates for the following posts on contractual and contractual basis as per the table below recruitment process for Nandurbar districts under National AYUSH Mission.
Diploma in Pharmacy, Degree in Pharmacy from a recognized University, Institution; Should be registered with the Pharmacy Council under Section 12 of Pharmacy Act, 1948.
B.Pharm/D.Pharm; The posts in the advertisement are not regular posts of the State Government but purely contractual posts. There will be no right to permanency in the said post and the service rules of the Government will not be applicable for these posts, also the applicant will not have the right to be included in the regular service of the Government or to claim protection of service through the Government or the same.
PhD in any branch of Life Sciences from a recognized university or equivalent with a minimum of three years of post- qualification research experience in the relevant field. At least one publication as first author in a scientific journal.
M.Sc, M.Tech Life Science, Bioscience, Biochemistry, Zoology, Biotechnology, Forensic Science; Knowledge in cell culture, hands- on in vitro and in vivo neuronal models, molecular biology techniques, Animal handling
B. Pharm, M. Pharm, B.Tech. experience supervising and controlling production areas like Aseptic Filling, Vial Washing, Autoclave and Lyophilizer. Exposure of machine qualification activity will be added advantage.
PhD. in Chemical, Biological, Pharmaceutical Sciences in relevant fields from a UGC, AICTE recognized University, Institute, Ten years post doctorate experience in research and development and, or scientific activities in relevant area of drug analysis out of which two years in a responsible capacity in scientific administration