MSN Laboratories Released Job Openings On 08/02/2022.MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has nine API and five finished dosage facilities established across Hyderabad, USA and Myanmar
Vacancy Details:
MSN Laboratories Recruiting B Pharma / M Pharma / MSc candidates with 03-08 Years Experience For API Regulatory Affairs,FR&D Dept Position.Complete Details for the API Regulatory Affairs,FR&D Dept as follows.
Important Details :
- Location : Hyderabad/Secunderabad
- Openings:60
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application: 08/02/2022
- Mode of application :Walk In
- Time And Venue: Walkin Interview on 11th February from 9.30 AM – 1.30 PM onwards,MSN Laboratories Pvt. Ltd, R&D Center, Pashamylaram (V), Patancheru (M), Sangareddy (D.t), Telangana 91-8452304799/4899 & 040-30438786
Related Job : 50 Freshers & Experienced Openings At MSN Laboratories Walk In on 11th Feb 2022
Job Description/Skills Required
Walk- In Drive For Formulation Research and Development – FR&D ( FR&DÂ –Â Oral Solid Dosage / Liquids Oral Dosage / Injectables) Department – Formulation Division- R&D Center – Friday 11-02-2022
Formulation R&D Department ( Formulations R&D) in Formulation Division – R&D Center.
1 ) Candidate Should have minimum 2 to 7 Years of experience in formulation development of solid oral dosage form for regulated market such as USA and Europe. Candidate should have exposure in handling various dosage forms such as tablets and capsules with exposure of scale up activities. Exposure to preparation documents such as MFR, BMR, PDR are consider as added advantage.
2 ) Candidate should have 2 to 7 Years of experience in solid oral dosage forms for regulated market such as USA, Europe, Australia, etc.. He should have exposure in handling various dosage forms like tablets and capsules (ER/SR, IR). Experience in handling MUPS project is an added advantage. He should have exposure in designing strategies, DOE/QbD based development, data compilation and interpretation, basic knowledge about bio study evaluation, etc. Should have scale up exposure for regulated markets and should have appropriate knowledge about regulated market requirement. Should have exposure in preparing and reviewing documents like PDR, MFR, BMR, etc. Supervising and knowledge about handling regulatory queries will be an added advantage
3 ) should have 2 – 7 years experience in FR&D (solids) should have knowledge in QbD & DoE & its application in Formulation Development. should have knowledge on regulatory guidance.
Click here for Official notification and ApplyÂ
Walk-In Drive For for API -Regulatory Affairs -Department in API Division – MSN R&D Center.
1. Collecting and reviewing the documents received from various departments R&D, AR&D, QA, QC and Production etc at each and every stage of manufacturing of drug substances to minimize the errors at the time of submission to regulatory agencies.
2. Hands on experience on the preparation of DMFs and their registration processes in the major regulatory regions [US, Canada, Europe etc]..
3. Hands on experience on preparation of drug master files, Applicants Parts, Tech Pack, life cycle management [updates and amendments] and drafting of response to deficiencies and customer DMF review comments for all global regions.
4. Should have hands on experience on eCTD regulatory submission tools.
5. Should have knowledge on the requirements to respond to the deficiencies.
6. Participation in the cross functional team meetings and providing regulatory inputs to the Product Development Teams.
Click here for Official notification and ApplyÂ
