Experience in operating and cleaning a Vial Washing machine, Oepyrogenation Tunnel, Automatic Vial Filling and Sealing Machines, and Automatic PFS filling machines 

Department Ophthalmology / Gynaecology / Multi-specialty; Market knowledge update, decision making skills, multi-tasking-planning & organizing, analytical skills, conceptual skills & creativity.

M.Pharm. QMS/AQA/IPQA/ Validation/Documentation. Candidates should have experience in Formulations regulated manufacturing company such as USFDA & MHRA. Exposure to regulatory audits like USFDA, MHRA is mandatory

B.Pharma / B.Sc; Trouble Shooter, Granulation, Compression, Coating, Machine Operators and Executives. Primary Packing, Secondary Packing. Hands on experience in HPLC, Chromatography Analyst, Trouble Shooting, and e-LIMS User, LCMS.

Hetero Drugs is an Indian pharmaceutical company and the world’s largest producer of anti-retroviral drugs. Heteros business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics.

Experience in Regulated Pharma company with knowledge of Manufacturing Process of Tablets, External Preparation and FDA

Having Injectable Experience of Shop floor activities like Vial washing and Depyrogenation, Filling and Sealing, Autoclave, Garment washing machine, Lyophilizes

Candidates having M.Sc, M. Tech, M. Pharm, M.V.Sc. or equivalent qualification in Life Sciences or allied subjects Biochemistry, Biotechnology, Virology, Bioinformatics, Computational Biology, Microbiology, etc with a minimum of 55% aggregate marks

M.Sc. in Chemistry, Organic Chemistry, Pharmaceutical Chemistry, Analytical Chemistry, Biochemistry, B.Pharma alongwith 02 years R&D experience in relevant area. 

Pass in D.Pharmacy, B.Pharmacy or Intermediate vocational course in Pharmacy recognized by Government of AP. Must be registered with the A.P. Pharmacy Council. In case of candidate possess both D.Pharmacy and B.Pharmacy, the maximum percentage secured in any of the above shall be considered.

PhD Pharmaceutical Sciences, Chemistry, Biochemistry a relevant branch of Engineering Industrial Experience min. 1 year in Formulation department of any Pharmaceutical company

M.Sc, M. Pharma, B. Pharma. Analytical methods validation, verification and methods transfer. Validation of cleaning methods. Handling HPLC, GC, DR and other instruments. Preparing method validation verification protocol and report. Reviewing analytical hard copy and electronics data.

Support Established Products technical functions in MEAP and APAC region for Abbott manufacturing facilities and TPMs. Provide technical support to cross-functional teams during test method development, validation, transfer, or problem solving for a given drug product primarily of Biosimilars & Injectables.

Environmental monitoring  Media fill visual inspection  Aseptic area monitoring  Handling of media fill activity  Aseptic area personal qualification

Effectively generate new business leads and opportunities from various sources and engage through proper prospecting, email campaigns, cold-calling and regular follow-ups

As an Associate Regulatory Affairs Director I, you will be a key contributor to regulatory submission strategy, identifying submission risks and opportunities. You will lead regulatory applications and manage procedures through approval.

Leading study setup, including TF design, database structure, specification, and obtaining and providing approvals as needed. Coordinating and documenting the receipt and processing of electronic or ancillary data received from outside sources

Applications are invited from the eligible candidates for filling up of various categories of posts in Urban Clinics/UPHCs under NUHM in Erstwhile Guntur District.