Founded in 2007, Biophore India Pharmaceuticals Pvt. Ltd has established itself as a trusted partner for niche and complex products. With 4 US FDA and EU approved API manufacturing facilities, one dedicated intermediate facility and a world class R&D lab housing 400 scientists with varied expertise, Biophore has emerged as one of the leading API companies globally.
DATE AND TIME:
DATE:10th May
TIME: 9.30 AM – 4.00 PM
VENUE:Plot no 231, IDA Phase -II, Pashamylarm, Patancheru (M), Medak District, Biophore Road, Pashamylaram, Telangana 502307
Contact – Bhavani Reddy
Prefers women candidates
EXP:2 – 5 years
SALARY:Not Disclosed
LOCATION:HYDERABAD
Job description
- Organizing, maintaining, and filing regulatory documents globally, ensuring compliance with regulatory guidelines.
- Prompt regulatory support to the customers.
- Collaboration & engaging in periodic customer teleconferences to resolve queries
- Change control evaluation and plant support
- Scheduling the life cycle management activities globally for all the regulatory submissions complying with region specific requirements
Ensure the Drug Master File (DMF) deficiency letters received from various regulatory agencies globally are responded in time with adequacy and accuracy
Role:
Legal & Regulatory – Other
Industry Type:
Pharmaceuticals & Lifesciences
Department:
Legal & Regulatory
Employment Type:
Full Time, Permanent
Role Category:
Legal & Regulatory – Other
Education:
M.Pharma, MS/M.Sc(Science) in Chemistry
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