Global Regulatory Jobs in India

About AstraZenecaAstraZeneca is a global science-led patient-focused biopharmaceuticalcompany that focuses on the discovery development and commercialization of prescription medicines for some of the worlds most serious diseases. But were more than one of the worlds leading pharmaceutical companies....

About Apotex Inc.Apotex is a Canadian-based global health company. We improve everyday access to affordable innovative medicines and health products for millions of people worldwide with a broad portfolio of generic biosimilar innovative branded pharmaceuticals and consumer health products. Headquar...

About Apotex Inc.Apotex Inc. is a Canadian-based global health company that produces high-quality affordable medicines for patients around the world. Apotex employs almost 7200 people worldwide in manufacturing R&D and commercial operations. Apotex medicines are accessible to patients in more than 7...

At EY were all in to shape your future with confidence.Well help you succeed in a globally connected powerhouse of diverse teams and take your career wherever you want it to go.Join EY and help to build a better working world.Solution Architect GMA - global medical affairs - GPS - global patient sa...

Job Description: Head of Projects (Technical Services)Location: Ahmedabad Reports to: Chief Technical Officer (CTO) Team Size: 50 Vertical: Technical Services (Formulation Manufacturing)Role OverviewWe are seeking a dynamic and experienced Head of Projects (Technical Services) to lead the creation o...

Job Description:Position: RA & QA AssociateLocation:DelhiWorking Days:5 Days Monday - Friday Timings: 9:00 AM 5:00 PMRole OverviewResponsible for regulatory submissions product registrations license renewals and compliance for medical devices in India and neighboring countries. Supports Quality M...

Additional Location(s):US-MN-Maple Grove; Canada-QC-Montreal; India-Maharashtra Pune; US-MA-WalthamDiversity - Innovation - Caring - Global Collaboration - Winning Spirit- High PerformanceAt Boston Scientific well give you the opportunity to harness all thats within you by working in teams of divers...

Responsibilities:Dossier Preparation:Compile review and prepare regulatory documentation ensuring accuracy and completeness.Collaborate with cross-functional teams to gather necessary information for dossier submissions.Maintain and update regulatory files and databases.DMF Management:Manage Drug Ma...

What youll do As an (Senior) Business Analyst in Regnology you will be part of ourinternational Research & Development Teamand youll work within ouragile development cyclein the RegTech area during on enhancing and re-launching our product calledRegnology Transactions.Your key...

Position Description:Company:Founded in 1976 CGI is among the largest independent IT and business consulting services firms in the world. With 94000 consultants and professionals across the globe CGI delivers an end-to-end portfolio of capabilities from strategic IT and business consulting to system...

We are currently looking for: Global IT Security Expert - IAM Position of broad specialization with main area focusing on Identity and Access Management (IAM). In this role employee will lead and advance the strategic security operations and engineering initiatives across GGH related to Identity an...

Job TitlePH Quality & Regulatory regional lead - JAPACJob DescriptionJob Title : PH Quality & Regulatory regional lead - JAPACJob Responsibilities: Ensures monitoring of global regulatory requirements for products by leading the development of monitoring systems delegating responsibilities and ensur...

Position Description:Position DescriptionCompany Profile:Founded in 1976 CGI is among the largest independent IT and business consulting services firms in the world. With 94000 consultants and professionals across the globe CGI delivers an end-to-end portfolio of capabilities from strategic IT and b...

Position Description:Position DescriptionCompany Profile:Founded in 1976 CGI is among the largest independent IT and business consulting services firms in the world. With 94000 consultants and professionals across the globe CGI delivers an end-to-end portfolio of capabilities from strategic IT and b...

Required Attributes : Masters degree/Ph.D in Biomedical Engineering Life Sciences Biotechnology or a related field. 6-10 years of experience in regulatory affairs and quality management within the IVD or medical device industry. In-depth knowledge of global regulatory standards and quality ma...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

We are seeking an experienced Restraints and Occupant Safety Engineer to join our Vehicle Safety team. The role involves end-to-end responsibility for occupant protection development including CAE test validation and regulatory/NCAP compliance for passive safety systems (airbags seatbelts seats). Ke...

Regulatory Affairs Team Leader Authoring. Role detailed classificationRegulatory Affairs AuthoringJob Summary: We are seeking highly skilled and experienced Life Sciences (LS) Regulatory Affairs (RA) Team Leader (TL) Authoring to join our LS Practice team. The successful candidate will be responsi...

Job Title: Regulatory Affairs Associate Authoring. Role detailed classificationRegulatory Affairs AuthoringJob Summary: We are seeking highly skilled and experienced Life Sciences (LS) Regulatory Affairs (RA) Associate Authoring to join our LS Practice team. The successful candidate will be respon...

Job TitleProduct Owner - IFUJob DescriptionJob title:You are a part of the IFU team in System Development Cluster within the R&D Department of the Image Guided Therapy (IGT) Business within Philips Healthcare. This Business Unit is responsible for marketing service development and manufacturing of I...