Medical Affairs Manager

Role - Regulatory Affairs - Medical Devices Experience - 1 to 3 Years Location- Madhavaram Chennai Budget - As per the industry Key Responsibilities 1 Regulatory Submissions Prepare and submit regulatory documents to authorities for approval such as new product applications amendments and supplements 2 Compliance Ensure products meet regulatory requirements...

We are in the process of hiring Regulatory Affairs **Job Title**: Regulatory Affairs Executive **Key Responsibilities**: **Qualifications**: Bachelor Degree in a related field such as Biomedical engineering, Mechanical engineering with minimum of 5 to 7 years’ progressive Regulatory affairs experience in medical device & quality...

Job Title: Senior Regulatory Affairs Team Lead Medical DevicesLocation: Chennai, IndiaDepartment: Regulatory AffairsExperience Required: Minimum 5 yearsReports To: Head of Regulatory Affairs / Director of Quality & RegulatoryJob Summary:We are seeking a highly skilled and experienced Senior Regulatory Affairs Team Lead to manage and lead our regulatory...

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds. ClinChoice, is searching for an Executive - Regulatory Affairs (PLMDS) to join one of our clients. **Main Job Tasks and Responsibilities**: - Complete...

**Medical Writer Immediate Joiner** **Job description** **Industry**: Pharmaceuticals, Cosmetics, Medical Devices, Food Supplement, Labeling and Scientific Communications **Position**: Intern **Reports to**: Pubrica Business Head **Work Schedule**: Full Time, Monday to Saturday, 10:00a.m. to 7:00pm. Hours may vary on occasion, depending on workload. Second...

**Medical Writer Immediate Joiner** **Job description** **Industry**: Pharmaceuticals, Cosmetics, Medical Devices, Food Supplement, Labeling and Scientific Communications **Position**: Intern **Reports to**: Pubrica Business Head **Work Schedule**: Full Time, Monday to Saturday, 10:00a.m. to 7:00pm. Hours may vary on occasion, depending on workload. Second...

**Medical Writer Immediate Joiner** **Job description** **Industry**: Pharmaceuticals, Cosmetics, Medical Devices, Food Supplement, Labeling and Scientific Communications **Position**: Intern **Reports to**: Pubrica Business Head **Work Schedule**: Full Time, Monday to Saturday, 10:00a.m. to 7:00pm. Hours may vary on occasion, depending on workload. Second...

**Medical Writer Immediate Joiner** **Job description** **Industry**: Pharmaceuticals, Cosmetics, Medical Devices, Food Supplement, Labeling and Scientific Communications **Position**: Intern **Reports to**: Pubrica Business Head **Work Schedule**: Full Time, Monday to Saturday, 10:00a.m. to 7:00pm. Hours may vary on occasion, depending on workload. Second...

Responsibilities High clinical quality in the Company’s programs and improvement in outcomes of patients participating in the programs Serve as professional anchor for the registration as Clinical Establishment including liaison with patient’s doctors where needed Primary Execute ongoing oversight on patient reviews by Clinical Pharmacists to ensure...

Company Description Bosch Global Software Technologies Private Limited is a 100 owned subsidiary of Robert Bosch GmbH one of the world s leading global supplier of technology and services offering end-to-end Engineering IT and Business Solutions With over 28 200 associates it s the largest software development center of Bosch outside Germany indicating that...