-
-
Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process, which may…
-
what is CRED? CRED is an exclusive community for India's most trustworthy and creditworthy individuals, where the members are rewarded for good…
-
Job Title: Regulatory Global Submission Manager Key Responsibilities In close collaboration with Regulatory Asset Oversight, GRL and RMT, provides project management support…
-
Job Title: Manager 2 Regulatory Labelling Business Unit: Clinical Development Job Grade G11A/11B Location : Gurgaon/Mumbai At Sun Pharma, we commit to…
-
Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the…
-
MEDICAL REPRESENTATIVE (ASSOCIATE) FOR A FASTEST GROWING PHARMACEUTICAL COMPANY FROM KOLKATA FOCUSING ON GASTROS,SURGEONS,GYNAE AND PHYSICIAN. Relationship Building: Build and maintain positive…
-
Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may…
-
The Position Although one or more potential candidates for this position have been identified, we will consider applications from any interested applicants."…
-
? Prepare, review, and submit DMFs/CTDs (USDMF, EDMF, CEP, etc.) for regulated and semi regulated markets ? Maintain regulatory documentation and lifecycle…
-
Job Title: Technical Documentation Specialist - CE Compliance Department: Compliance / Regulatory Affairs / Engineering Location: Mohali Sector 82 Employment Type: Full…
-
-
Position Overview: The Drug Regulatory Affairs Executive plays a critical role in ensuring that pharmaceutical products meet all regulatory requirements. This position…
-
Perform case processing of Adverse Event (AE) reports from various sources (spontaneous, literature, clinical trials). Enter and update safety data into safety…
-
Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process, which may…
-
Job Overview Under general supervision, Prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization activities for either internal…
-
Job Title: Assistant Manager - Drug Regulatory Compliance Industry: Pharmaceuticals Experience Required: 3-5 Years Job Summary: We are seeking a detail oriented…
-
Job Description: 1. New submissions: a. Review & prepare CMC (Chemistry, Manufacturing and Controls) dossiers for fresh submissions. b. Review documents (Development…
-
We are looking for RA executives with 2 5 years experience in EU Submissions or at least with Drug product submissions to…
-
Why join Stryker? Looking for a place that values your unique talents? Discover Stryker's award winning culture. We are proud to offer…
-
Compile, prepare, review and submit ANDA submissions and Amendments to FDA with an overall objective to avoid major deficiencies and contribute to…
-
DigitalX our new information technology function is spearheading this value driven transformation across Astellas. We are looking for people who excel in…
-