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  LUPIN LIMITED - Urgent Openings for Pacing / Regulatory Affairs Departments - Apply Now

Interested candidates can share with the below-mentioned mail-Id:  raghu@virchowbiotech.com Raghurami Reddy Palugulla, Sr. Manager-HR, Virchow Biotech Pvt. Ltd –Hyderabad., Mob- 09642996045  

 

 

 

 

 

 

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  REGULATORY AFFAIRS/EXPERIENCE-BULK DRUGS/API-HYDERABAD Department: Regulatory Affairs Designation: Executive/Sr. Executive Industry: Pharma/API Experience: 2 to 6 years CTC: Negotiable Job Location: Sanath Nagar, Hyderabad Roles and Responsibilities Preparation of Drug Master Files (DMF) in CTD / eCTD / Nees format for US, European Countries, Canada, Australia, Japan, GCC, Turkey and Korea as per customer/ business requirement. Preparation of amendments/ Annual Reports to USDMFs, CEP variations, EDMF Updates, Biannual updates to Canada DMFs and Annual updates to Korea DMFs, Japan DMFs. Review and approval of change controls. Submission of notifications to the customers pertaining to regulatory submissions as per the applicability. Responding to deficiency letters received from various regulatory agencies like USFDA, EU Agencies, TGA, Health Canada etc. Hands-on experience in Electronic submissions-Lorenz. Maintaining query database and response timelines. Tracking of variation submis

  Walk- In Drive for Regulatory Affairs Dept. in API Division- R&D Center. Regulatory Affairs API RA Dept. in API Division, Openings: 70 Job Title: Executive / Senior Executive Experience: 1 to 8 years in API RA field Education: B Pharma / M Pharma / M.Sc Department: Regulatory Affairs Job Profile: 1. Collecting and reviewing the documents received from various departments R&D, AR&D, QA, QC and Production etc at each and every stage of manufacturing of drug substances to minimize the errors at the time of submission to regulatory agencies. 2. Hands on experience on the preparation of DMFs and their registration processes in the major regulatory regions [US, Canada, Europe etc].. 3. Hands on experience on preparation of drug master files, Applicants Parts, Tech Pack, life cycle management [updates and amendments] and drafting of response to deficiencies and customer DMF review comments for all global regions. 4. Should have hands on experience on eCTD regulatory submission t

  Accuprec Research Labs is hiring in multiple Domains! Accuprec Research Labs Pvt. Ltd.® is a service provider for various testing services required for pharmaceuticals, chemicals and phytochemicals as well as herbal formulations. Job Opening for below Positions: • Genotoxicology • Quality Assurance • ADL • Formulation Development • Pharmacology & Toxicology • Accounts • IT • DCO Interested candidates send your updated resume to  👉 career@accuprec.in  along with mention the below details, -Current CTC -Onhand salary -Expected Salary -Notice Period

Intas Pharmaceuticals Ltd - Openings for R&D (Analytical) / Manufacturing / Quality Control / Regulatory Affairs - Apply Now

  HETERO Biopharma - Urgent Openings for Quality Control - Apply Now

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  Walk -in Interview for API Quality Control (2-6 years) on 20th Feb’ 2021 Openings: 10 Roles and Responsibilities : Handling instrumentation analysis for raw materials, stability samples, inprocess, intermediate samples and finished products of the instruments UV, GC, and HPLC. Calibration of HPLC, UV, GC Weighing Balance, Analytical Balance, Micro Balance, pH meter, Conductometer. Reagents preparations and maintenance of related records. Maintaining online entries of Reference/Working standards, instrument log books etc. Preparations of SOPs, Specifications, STPs and GTPs. Maintaining Good Laboratory Practices. Maintaining Good Documentation Practices. Maintaining Hygienic conditions and following dress code in QC laboratory. Maintaining related raw data and logbooks. Informing OOS, OOT, OOC, Incidents and Deviations to supervisor. Volumetric solutions preparations, standardizations and maintenance of related records. Desired Candidate Profile Qualification: B.Sc/ M.Sc. Experience: 2

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Walk-in-interview for QC - IP & FG and QA- IPQA & Validation on 14th Feb 2021 at Bachupally, Aurobindo, Unit 3

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ORBIT PHARMACEUTICALS - Walk-In Interviews for Freshers & Experienced in Regulatory Affairs / Business Development on 12th Feb' 2021

  Glenmark is hiring for "Officer - Regulatory Affairs (US Market) Location: R&D Centre Taloja. Interested candidate can share their resume at  Simran.Gill@glenmarkpharma.com

NOVICK BIO-SCIENCES - Walk-In Drive for Freshers & Experienced Chemist / Research Associate / Associate Scientist / Scientist - R&D on 13th Feb' 2021

  Aurobindo Pharma Ltd - Multiple Openings for Regulatory Affairs - Formulations

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