... with 2+ direct reports - Regulatory affairs expertise in drug, biologic, or medical device approvals - Knowledge of product registration, submissions, and regulatory strategy - Experience serving as regulatory liaison with agencies and internal teams - Understanding of manufacturing, CMC, labeling, and regulatory interpretations ...
Senior Regulatory Affairs Specialist supporting medical device regulatory submissions and compliance at a global healthcare technology company. The role involves managing regulatory documentation, coordinating with health authorities, and maintaining compliance systems across international markets. Responsibilities - Establish ...
Nānakrāmguda, भारत
View vacancyMedtronic seeks a Senior Regulatory Affairs Specialist in Gurgaon to lead regulatory strategies for medical device product portfolios in India. The role manages registrations, submissions, and compliance activities while partnering with global and local teams to support market access and product lifecycle management. Responsibilities ...
Gurgaon, भारत
View vacancyAbbott seeks an Assistant Manager in Regulatory Affairs to manage global labeling portfolios, maintain compliance documentation, and support product registrations across international markets. The role involves developing core data sheets, coordinating with cross-functional teams, and providing regulatory guidance to affiliates ...
AstraZeneca seeks a Regulatory Affairs Manager I to lead end-to-end planning and execution of global regulatory deliverables for established pharmaceutical products. This individual contributor role involves managing submissions, labeling strategy, and cross-functional coordination across multiple regions with minimal supervision. ...
Bangalore, भारत
View vacancyAstraZeneca seeks a Regulatory Affairs Manager II to lead end-to-end planning and execution of global regulatory deliverables for established pharmaceutical products. The role manages moderate to complex submissions, labeling maintenance, and cross-functional coordination across regions as an individual contributor within ...
Bangalore, भारत
View vacancyRegulatory Affairs Specialist at Masimo (Danaher) responsible for obtaining and managing Indian regulatory clearances for medical device products. The role involves supporting APAC regulatory filings, maintaining product registrations, and serving as the primary regulatory representative for project teams. Responsibilities ...
Bangalore, भारत
View vacancy... Job Description - Supports the preparation of documentation and submissions under EUCTR guidance. - Coordinates and manages client deliverables supporting regulatory compliance. - Liaises with internal and external clients in the tracking and status update of project plans and overall support of projects. - Maintains knowledge ...
Bangalore, भारत
View vacancyPosition: Regulatory Affairs Specialist Location: Kochi Qualification: Bachelor's degree in Regulatory Affairs, Biomedical Engineering, Engineering, Life Sciences, or related field Experience: Min 3 years of Regulatory Affairs experience in the medical device industry Salary : 8 LPA (Negotiable) Job Summary: We are looking ...
Ernakulam, भारत
View vacancy... by Mastery, Impact and Respect, we continuously improve, focus on meaningful results and collaborate with trust and openness. Become part of our team as a Regulatory Affairs Specialist. Job Purpose The responsibility of the Regulatory Affairs Specialist is to support customers’ requests regarding referencing of Datwyler ...