USV Pvt. Ltd Released Job Openings On 02/09/2022.USV Pvt. Ltd is an Indian multinational pharmaceutical and biotechnology company in Mumbai, India. The company operates across 75 countries globally, and is a leading producer of Metformin in India. The company was founded by Vithal Balkrishna Gandhi to provide affordable and quality healthcare to every Indian..Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for USV Pvt. Ltd Recruitment 2022 are provided below. Interested and eligible candidates can submit application along with resume.Â
Vacancy Details:
USV Pvt. Ltd Recruiting M.Pharm,M.Sc Candidates with 02-04+ Years of Experience for Regulatory Affairs – API – Executive Position.Complete Details for the Regulatory Affairs – API – Executive Departments as follows.
Important Details :
- Location :Mumbai( Govandi )
- No of Vacancies: NA
- Details of Salary: NA
- Opening date for online Application:02/09/2022
- 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
Related Job : 50+ Openings : QC,QA,R&D,Production,AR&D,Purchase,Warehouse,HR Walk In 3rd to 5th Sept 2022 At Manvi Biopharma Pvt. LtdÂ
Job Description/Skills Required
- Collect / Prepare and file dossiers in a timely & accurate manner for Formulation & API product to get licenses from various targeted markets.
- Review & regulatory impact analysis of the change control, communication with customer for notification and approval as applicable
- Review and regulatory impact analysis of the changes notified by the vendor as per current regulatory requirements (country specific), as desired.
- Evaluate any changes proposed post-approval. Prepare and file necessary amendments/ supplements/ annual reports as applicable to ensure regulatory compliance (Post-approval Life Cycle Management)
- Prepare the checklist for documentation for regulatory fillings as per current regulatory requirements.
- Collect & conduct first-level review/ overview of relevant standard technical documentation like stability, TTD, PDR, method validation.
- Conduct initial review of labeling/ artwork as per the market where the dossier is being filed
- e-CTD compilation/ publishing of DMF/ Dossier & Submission to customer/ Health Authorities
- Assist in resolution of queries received from customer/ agency/ regulator and assessing them before sharing with team leader
- Preparation of Tech-packs for APIs
- Prepare & e-file documents for registration of any facility used (in process for drug) with USFDA
- Submission of Renewals, Re-registrations, Tender
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