HRD House Released Job Openings On 29/08/2022.Talent Search & Placements In Pharmaceutical, Nutraceuticals, OTC, Bulk Drugs and Chemical Companies at all levels & across the functions..Application form link provided at the end of post. Eligibility for the Regulatory Affairs Manager as follows.
Vacancy Details:
HRD House Recruiting B.Pharma,M.Pharma,M.Sc Candidates with 15-10 Years Experience for Head – Regulatory Affairs Position.Complete Details for the Head – Regulatory Affairs as follows.
Important Details :
- Location : Nasik/Nashik
- No of Vacancies: NA
- Details of Salary: ₹ 20,00,000 – 25,00,000 P.A.
- Opening date for online Application: 29/08/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
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Job Description/Skills Required
You will be responsible for,
- 1. Candidate will be responsible for Preparation & review of product registration/renewal of
- dossiers (CTC/ACTD) for Asian & African countries (ROW).
- 2. Candidate will be responsible for heading the RA Dept. activities with respect to dossier
- preparation for registration/renewal of registration, manufacturing license with products, WHO-
- GMP Certificate, MSO registration, etc.
- 3. Candidate will be responsible for to obtain additional product permissions, test license,
- certificates, export NOCs from CDSCO, COPPs, plan approvals, technical staff registration and
- approval, public testing labs approval, etc.
- 4. Candidate will be responsible for to submit the required information to regulatory authorities.
- 5. Candidate will be responsible for Obtain product permissions, test license, plan approval, etc.
Required Candidate profile
- 1. Candidate is B.Pharma / M. Pharm / M.Sc with minimum 15+ years experience in Plant Regulatory Affairs in Pharma Formulation for ROW Market.
- 2. Preparation & review of product registration/renewal of dossiers (CTC/ACTD) for Asian &
- African countries (ROW).
- 3. To ensure regulatory compliance as per D&C Act and Marketing authorizations.
- 4. To check the artworks for compliance with regulatory and pharmacopoeia requirements of
- products.
- 5. To ensure regulatory compliance as per D&C Act and Marketing authorizations.
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