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: AFFAIRS-API/BULK DRUGS/REGULATORY AFFAIRS-EXECUTIVE/SR.EXECUTIVE-API/EXECUTIVE – QUALITY ASSURANCE-FORMULATION
- Qualification : M.Pharma/B.Pharma/MSC/Any Graduate
- Experienced:0-6 yrs
Job Description: Greetings from HETERO LABS LIMITED.. !
Important Details :
Work Location: Hyderabad/Secunderabad ( Balanagar)
Post of date:01/09/2023
Selection Process: The selection will be on the basis of Interview.
Mode of Interview: Face To face Interview
Interview Rounds of Interview: HR
REGULATORY AFFAIRS-API/BULK DRUGS-HYDERABAD
Preparation, compilation and submission of Drug Master File for China, Japan, US and Europe market.
2. Preparation of response to the Agencies, Agent and Customer queries.
3. Being updated with relevant regulatory guidelines.
4. Discuss and co-ordination with cross- functional teams i.e. plant QA, QC, synthesis (CRD
and ADL) for carryover studies and finalization of DMF documents.
5. Review of regulatory documents on receipt from various departments before inclusion in DMF.
6. Control strategy, KSM evaluation and intermediate specification proposal received from CRD for new
projects filing.
Maintaining a data base to keep track of submissions, amendments and approvals.
Interested Candidates please share your Updated Resume At vivek.s@hetero.com
REGULATORY AFFAIRS-EXECUTIVE/SR.EXECUTIVE-API-HYDERABAD
Depratment:Regulatory Affairs/API
Qualification:M.Pharma/B.Pharma/MSC
Experience:1 to 5 Years
Salary : Negotiable
Location:Hyderabad
Job Roles&Responsibilities
Preparation, compilation and submission of Drug Master File for China, Japan, US and Europe
market.
2. Preparation of response to the Agencies, Agent and Customer queries.
3. Being updated with relevant regulatory guidelines.
4. Discuss and co-ordination with cross- functional teams i.e. plant QA, QC, synthesis (CRD
and ADL) for carryover studies and finalization of DMF documents.
5. Review of regulatory documents on receipt from various departments before inclusion in DMF.
6. Control strategy, KSM evaluation and intermediate specification proposal received from CRD for new
projects filing.
Maintaining a data base to keep track of submissions, amendments and approvals.
Interested Candidates please share your Updated Resume At vivek.s@hetero.com
EXECUTIVE – QUALITY ASSURANCE-FORMULATION-HYDERABAD
Vacancy For Sr. Officer/Executive –Quality Assurance-Formulation-Hyderabad.
Position-Quality Assurance
Exp-1-6yrs
Location -Hyderabad
Designation- Sr.Officer/Executive
Having knowledge on GMP guidelines, Intiation and closure of change controls, incidents, CAPA, review and approval of formulation stability data and validation protocols, reports and raw data.
Interested candidate please update resume email id: Prahalad.U@hetero.com
ABAC
