job Description:
Key Responsibilities:- Responsible for preparation applications for obtaining Manufacturing licences, BE-NoC, CT-NoC, WHO GMP, CoPP
across all dosage forms & API
manufacturing locations
- Responsible for the maintenance of import licences for developmental purpose
- Responsible for review of Plant related documents (MFR, PVP,PVR, Stability protocols, Specifications)
Job Requirements
Technical Requirements:
- Understanding of various dosage forms, their development and bulk active manufacturing
- Knowledge of Manufacturing work orders, PVP, PVR, Stability protocols
- Hands on experience of current GMP/GLP requirements and their compliance
- Knowledge of change control management
Key Attributes:
- Excellent planning & organizing skills with attention
- Good people development skills including ability to learn & understand the regulatory guidelines
- Consistent focus on performance, project goals and outcomes
- Collaborative skills
Operating Network:
Internal: Product Development Teams, GG-India marketing teams, Corporate Legal, Plant QA personnel,Corporate Affairs,
FTMR, RA (Other regions), LL QA, Contract Mfg Team, SCM
External: DCG(I), State DCA & Narcotics Department
Educational Qualifications: Masters in Pharmaceutics/Chemistry with about of 7-8 years experience in the Pharmaceutical
Industry preferred.
Experience Required: 8 years experience in manufacturing operations.
across all dosage forms & API
manufacturing locations
- Responsible for the maintenance of import licences for developmental purpose
- Responsible for review of Plant related documents (MFR, PVP,PVR, Stability protocols, Specifications)
Job Requirements
Technical Requirements:
- Understanding of various dosage forms, their development and bulk active manufacturing
- Knowledge of Manufacturing work orders, PVP, PVR, Stability protocols
- Hands on experience of current GMP/GLP requirements and their compliance
- Knowledge of change control management
Key Attributes:
- Excellent planning & organizing skills with attention
- Good people development skills including ability to learn & understand the regulatory guidelines
- Consistent focus on performance, project goals and outcomes
- Collaborative skills
Operating Network:
Internal: Product Development Teams, GG-India marketing teams, Corporate Legal, Plant QA personnel,Corporate Affairs,
FTMR, RA (Other regions), LL QA, Contract Mfg Team, SCM
External: DCG(I), State DCA & Narcotics Department
Educational Qualifications: Masters in Pharmaceutics/Chemistry with about of 7-8 years experience in the Pharmaceutical
Industry preferred.
Experience Required: 8 years experience in manufacturing operations.
Salary:Not Disclosed by Recruiter
Industry:Pharma / Biotech / Clinical Research
Functional Area:Legal, Regulatory, Intellectual Property
Role Category:Drug Regulatory Affairs/Documentation
Role:Regulatory Affairs Manager
Keyskills:Regulatory Affairs, cmc documentation, regulatory compliance, registration, ctd
Desired Candidate Profile
Education:(UG - B.Sc - Any Specialization, Chemistry, B.Pharma - Pharmacy) AND (PG - M.Sc - Any Specialization, Chemistry, M.Pharma - Pharmacy) AND ( Doctorate - Ph.D - Advertising/Mass Communication, Chemistry, Pharmacy)
Please refer to the Job description aboveCompany Profile
Dr. Reddy's Laboratories Ltd.
http://www.drreddys.com
Dr Reddy's is a global, vertically integrated pharmaceutical company with a presence across the value chain, producing and delivering safe, innovative, and high quality finished dosage forms, active pharmaceutical ingredients and biological products. Our products are marketed across the globe, with an emphasis on North America, Europe, India, Russia and other emerging markets. We conduct NCE drug discovery research in the areas of metabolic disorders and cardiovascular indications at our research facilities in Atlanta (USA) and Hyderabad (India). Through our Custom Pharmaceutical Services business unit, we provide drug substanceand drug product development and manufacturing services on a proprietary basis.http://www.drreddys.com
Contact Details
Recruiter Name:Ajitabh Sinha
Contact Company:Dr Reddys Laboratories Ltd
Address:Ankur, Plot No. 187-A, Road No. 13, Jubilee Hills HYDERABAD,Andhra Pradesh,India
Telephone:91-40-44346576
Source: http://jobs.doyouknow.in/Openings/Hyderabad/Pharma-Jobs/Dr-Reddys-Laboratories-Ltd-Opening-For-Regulatory-Affairs.aspx
Source: http://jobs.doyouknow.in/Openings/Hyderabad/Pharma-Jobs/Dr-Reddys-Laboratories-Ltd-Opening-For-Regulatory-Affairs.aspx
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