Hetero Drugs Walk In Interview 2023. Hetero Drugs Notification full details below.Interested and eligible candidates can attend interview on scheduled time and venue.Hetero is an Indian pharmaceutical company and the world's largest producer of anti-retroviral drugs. It is also among the world's leading producers of key Active Pharmaceutical Ingredients with presence in 145+ countries and backed by 30 years of experience in the pharma sector.
Vacancy details:
- Department: Regulatory Affairs-API/Bulk Drugs/Sr.Executive/Asst.Manager-API/AR&D
- Qualification: B.Pharma/M.Pharma/MSC
- Experienced: 1-10 year(s) of experience
Job Description: Greetings from HETERO LABS LIMITED.. !
Important Details :
- Work Location: Hyderabad/ Secunderabad,Telangana
- Post of date:01/07/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To face Interview
- Interview Rounds of Interview: HR
HETERO – Walk-In Interview Details
We have Openings in Regulatory Affairs-API/Bulk Drugs
Experience(Requried):1 to 10 Years
Qualification:MSC/M.Pharma/B.pharma
Salary :Negotiable
Greeting from Hetero Labs-R&D (Formulation)
Immediate Opening for AR&D(Formulation) Position.
Department: AR&D
Designation: RA-I/RA-II
Experience: 2 to 5 Yrs
Job Location: Hyderabad
Area of Work
Analytical Method development .
Handling HPLC, GC, UV, IR, KF , Dissolutions
Interested Candidates please share profiles to edukondalu.m@hetero.com
Roles and Responsibilities
Regulatory Affairs-API(EXEPERIENCED ONLY)
Industry: Pharma Industry
Qualification: M.Pharma/B.Pharma/MSC
- DMF Compilation, Review and Submission in eCTD format to Various regions like USFDA, EDQM, EU, TGA, TPD and other regulatory authorities by ensuring compliance with regulations pertaining to respective Health authorities and ICH guidelines.
- Responsible for handling and submitting of various deficiencies received form regulatory bodies & customers on Drug Master Files.
- Submitting the DMF fee reimbursement through Pharmexcil and collecting, reviewing documents from respective departments.
- Coordination and supporting internal formulation CFT teams with API requirements / documents.
- Regulatory support and review for pre-filing and development documentation.
- Search and review published literatures related Clinical and Nonclinical data.
- Compilation of Dossiers and quality documents as per checklist in the guidelines.
- Preparation and review of Quality Documents.
- Preparation, Review and Submission of Dossiers as per CTD/ACTD /eCTD guidelines as well as country specific guidelines.
- Authoring, Compilation and review of ANDA dossier in eCTD format, followed by publishing, validation and submission of dossier.
- Ensure regulatory compliance by completing the appropriate filings and documentation pertaining to product registrations / approvals, as required by procedures relating to the regulatory requirements.
Desired Candidates Please Share your Updated Profiles to vivek.s@hetero.com
Note: Only Experienced Candidates Required.Freshers Don't Apply for this Job
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