Sun Pharmaceutical Industries Ltd Walk In Interview 2023. Sun Pharmaceutical Industries Ltd Notification full details below.Interested and eligible candidates can attend interview on scheduled time and venue.Sun Pharma is the fourth largest generic pharmaceutical company in the world. It is also India’s largest and most valuable pharmaceutical enterprise by size and market capitalization. The company provides high quality medicines trusted by customers and patients in over 150 countries and has multiple manufacturing facilities and R & D centers.
Vacancy details:a
- Department:– Executive- Regulatory Affairs
- Qualification: B. Pharm/M. Pharm/B. Tech (Food Technology)/MSc. (Food Technology)
- Experience :2-7 years
Job Description: Greeting from Sun Pharmaceutical Industries Ltd !!!!
Important Details :
- Location: Baroda
- Post of date:30/10/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face interview.
- Interview Rounds of Interview: HR
Job Responsibilities:
Evaluate composition of all food products (like health supplements, nutraceuticals, FSMP, FSDU and others).
Review label of food products, as per Food Safety Standards (Labelling and Display) Regulations.
Apply for license of food products on FoSCoS portal.
Submit Annual Return of Food Products.
File for approval of Food Ingredient under Food Safety and Standards (Approval for Non-Specified Food and Food Ingredients) Regulations.
Prepare product information, safety and claims support data for food products.
Preparation of import license application of Drugs.
Preparation of manufacturing license application of Drugs.
Preparation of Prescribing Information of Drugs.
Preparation of application for grant of BE permission for Drugs.
Duration Required: 31st October 2023
Send your resume to [email protected]
Job Description:
1) Compilation and submission of US- ANDA, DCP and ANDS dossier for US, Europe and Canada
2) Compilation and review of the dossier submissions documents like product development report, specification and analytical procedure, etc
3) Review and Compilation of deficiencies response for EU, US and CA
4) Compilation and submission of Annual report, variation & supplement for the US, EU & Canada
5) Well-versed with all regulatory guidance requirements and with eCTD compilation and RIMS
Send your resume to [email protected]
Note : Freshers need not apply
