Ind Swift Laboratories Jobs - Vacancies for Formulation in Drug Regulatory Affairs
Ind Swift Laboratories Jobs Opening 2022- Careers at Ind Swift Pharmaceuticals company, Grab this career opportunity to work in Ind-Swift Laboratories Ltd. Ind Swift Laboratories hiring for Freshers and Experienced Jobs candidates to work with the Company Pharma posting new jobs Vacancy frequently as per availability of vacant post, Here you can check eligibility criteria and qualifications, experience required for the position, and jobseeker candidates can Apply Online or Offline or by scheduled walk-in interview for Current Job Openings find more Pharma Jobs post.
About
Ind-Swift Laboratories Ltd. was named after the Bird “Indian Swiftlet” that is amongst the fastest flying bird in the world spending most of its life flying in air from which we derive our philosophy of inception that lies in speed, growth and persistence. Twenty Years on, what has stayed in our organization’s inheritance is the same spirit of flying high with pride. We are today an integrated pharmaceutical organization with global footprints.
Interested & eligible candidates need to apply online/offline via the given official website/address. You will get brief information on Ind Swift Laboratories jobs openings like educational qualifications, selection process, eligibility criteria, and important dates given in the below article. So read this article till the end to get all the information regarding this recruitment. For more jobs visit www.tyropharma.com.
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Ind-Swift Laboratories Ltd Jobs. Hiring for Formulation Site in Drug Regulatory Affairs- Executive/ Officer/ Sr. Officer
OPEN POSITIONS for Formulation Site
Drug Regulatory Affairs (Executive / Officer / Sr. Officer)
B Pharma / M Pharma with 3-5 years of experience
Job Location: Panchkula (3) & Gurugram (3)
Responsibilities :
1. Preparation and review of registration dossiers as per CTD/ACTD and country specific formats.
2 Review of quality documents like API’s DMF, Finished Product Specification, Certificate of Analysis, BMR, BPR. Process Validation and Stability etc. for guidelines Compliance.
3. Plan and coordinate with various departments like QA, QC and Production, to project the document requirements for appropriate submissions
4 Co-ordination with clients for the tracking and status update of project plans. eries raised 5. Preparation of response to queries I by regulatory authorities as well as by clients.
6. Preparation of Product Questionnaire, MAF and all related documents for bidding of international tenders. 7. Literature search/survey to compile clinical and non-clinical part within registration dossiers.
8. Preparation and review of SPC, Product monograph, package insert and labeling information. 9. Involved in drafting & review of applications for Product Approval, CPP, MMC, Non-Conviction Certificate and FSC
10. Involved in preparation of renewal application for certificates like GMP, CPP WHO-GMP, GLP & Non- Conviction Certificate
Note : Only MHRA, EU GMP & ROW exposure candidates will be entertained.
Selection Process
- Based on Written / Personal Interview
How to Apply
- Interested candidates fulfilling the eligibility criteria can apply for this job.
- Candidates can easily apply online through the following link. You can also visit the company's official website career page for further details.
- If a job opening is scheduled Walk-in-Interview then candidates are requested to read Walk-in Date, Time & Venue carefully.
- Open Positions for Formulation site in Drug Regulatory Affairs. Candidate can contact at;+91-7087978441 hr.gbu@indswiftlabs.com
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