First Class Post Graduate Degree, including the integrated PG degrees, with three Years Experience or PhD. Second Class Post Graduate Degree, including the integrated PG degrees, with PhD and three Years Experience
Good Academic record with at least 70% marks in Masters Degree in Life sciences, Microbiology, Biotechnology, Chemistry, Physics, Biochemistry are eligible to apply.
Ensure preparation, review and submission of CTD sections in compliance with requirements of EMA, USFDA and other global markets. Timely update and preparation of dossier and documents as well as responses to the queries raised by regulatory agencies
Must have experience in the development of nasal spray, nebuliser and other respiratory dosage form. Exposure of regulated and domestic product development
Planning and execution of batch packing activities such as Dispensing & Line clearance. Expertise in handling Blister, Bottle and Sachet packing machineries like BQS, CAM, Maspack, Auto Cartonator etc.
Review all data and documents related to product registrations for various health authorities. Compile registration dossiers for submission to various health authorities like – US, Canada, Europe, Australia
Diploma in Pharmacy or Bachelor of Pharmacy from AICTE approved Institutions. Registered as a Pharmacist under Section 31 or 32 of the Pharmacy Act, 1948 but excluding clause of Section 31 of the said Act.
District Welfare Association Thanjavur District. Medicine is a department of public welfare. Completed applications are invited to fill the vacancies mentioned below in Urban Health Centers, Rural Health Centers and Local Government Primary Health Centers in Thanjavur district on contract basis within 18.10.2024 by 5.00 p.m
A Scientific Professional with Bachelor, Masters degree in Pharmacy, Life Sciences, Chemistry, Biological Sciences with a business management degree, MBA is preferred. A minimum of 9 years experience with at least 5 years in a technical field analytical background and at least 4 year of experience in a customer facing role.
Co-ordination with product development team to keep track of various projects. Sample seeding from suppliers for project initiation. Co-ordination with supplier, principle for arranging quality documents.
Ensure outcomes of variations are communicated in timely manner and databases/lists are up to date at all times, in accordance with agreed procedure as applicable
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.