Hetero Drugs Ltd Released Job Openings On 19/05/2022. Hetero Drugs Ltd is an Indian pharmaceutical company and the world’s largest producer of anti-retroviral drugs. Hetero’s business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics.Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Hetero Labs Recruitment 2022 are provided below. Interested and eligible candidates can submit application along with resume.
Vacancy Details:
Hetero Drugs Ltd Recruiting B.pharma,M.Pharm,M.Sc Candidates with 03-08+years of Experience for Regulatory Affairs Department.Complete Details for the Regulatory Affairs as follows.
Important Details :
- Job location : Hyderabad/Secunderabad
- No of Vacancies:NA
- Details of Salary: NA
- Opening date for online Application: 19/05/2022
- How To Apply:Desired Candidate Please Share Your Profile vivek.s@heterodrugs.com
Related Job : IQVIA Released Work From Home Job Opportunity For B.Pharma,M.Pharma,M.sc,BHMS,B.U.M.S
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Job Description/Skills Required
- Preparation and review of Dossiers as per the current prescribe ICH guidelines for the
- ASEAN, African, CIS, Europe & Latin American Countries,Brazil,UAE
- • The List of Countries are mention below-
- • ASEAN- Malaysia, Vietnam, Philippines, Myanmar and Cambodia.Africa- Tanzania, Uganda, Ethiopia, Kenya, Rwanda, Ivory coast, Cameroon, Burkina Faso, Benin, Togo, Mali, Chad, Madagascar, Gabon, Senegal, Guinee, Niger and Congo.CIS- Ukraine, Uzbekistan, Moldova, Kazakhstan, Kyrgyzstan, Tajikistan, Armenia,Azerbaijan, Georgia and Belarus.Europe- Portugal, Malta, Italy, Austria, Germany.Latin America-Bolivia, Dominique Republic, Haiti
- • Provided Regulatory guidance and expedite response to regulatory authorities and Ensured documentation complies with regulatory agencies.
- • Filling the post approval variation of Type IA, Type IB & Type II, and Grouping of Variations.
- • Review of Quality and analytical data as per the pharmacopeia, specification, MOA, STP,
- Annual product report, Change control documents, Batch Record, Stability, Finish products/Packing material data for the purpose of compilation of the dossier.
- • Review of documents required for regulatory agencies (Viz , Analytical report, Process validation Protocol, process validation Report, Pharmaceutical development report, Protocols & stability data)
- • Preparation of various Pharmacological, Preclinical & Toxicological data based on published literature.
- • Preparation and review of labeling & packing materials and packing inserts of Finish formulation.
- • Preparation and review of SPC, packing insert and labeling information.
Click here for Official notification and Apply
