Medical Affairs Manager
4 weeks ago
A Medical Affairs Manager will develop and execute medical strategies, ensuring scientific and regulatory compliance, and serving as a medical expert for internal and external stakeholders.About the RoleKey responsibilities involve managing clinical trial activities, creating and approving promotional materials, and building relationships with healthcare professionals and key opinion leaders. They also collaborate with other departments, provide medical training, and oversee publication processes.Job Location - KolkataResponsibilitiesStrategy and planning: Develop and implement medical strategies that align with the company's commercial and clinical goals.Medical expertise: Serve as a scientific and clinical expert, providing medical input on product development and strategy.Regulatory compliance: Ensure all medical content, activities, and materials comply with industry standards and regulations.Clinical trial management: Plan, coordinate, and oversee clinical trials, including investigator-initiated studies.Medical education: Develop and deliver medical education programs and scientific exchange events for internal teams and external healthcare professionals.Stakeholder engagement: Build and maintain relationships with key opinion leaders (KOLs), medical societies, academic institutions, and other external stakeholders.Cross-functional collaboration: Work closely with other departments like marketing, regulatory, and clinical development to provide medical insights.Content and publication oversight: Approve promotional materials and oversee the publication of scientific data in manuscripts, abstracts, and presentations.Training and support: Provide scientific and clinical training to internal teams. QualificationsAdvanced degree in a relevant scientific or medical field (e.g., MBBS, M.D.). Required SkillsStrong understanding of clinical research and regulatory requirements.Excellent communication, presentation, and interpersonal skills.Ability to collaborate effectively with cross-functional teams.Project management and leadership skills.
-
Regulatory Affairs Associate
3 days ago
Madurai, India HCLTech Full timeExperience: 2 to 5 yearsEducation: Bachelor's degree in Biomedical, Mechanical, or B.PharmWe are looking for talented professionals for roles in Quality Assurance, Regulatory Affairs, and Documentation in the Medical Devices domain.Skills & Requirements:Minimum 3 years of experience in Medical Devices Regulatory Affairs, Quality Assurance, or Documentation...
-
Regulatory Affairs Associate
3 days ago
Madurai, India HCLTech Full timeExperience: 2 to 5 yearsEducation: Bachelor's degree in Biomedical, Mechanical, or B.PharmWe are looking for talented professionals for roles in Quality Assurance, Regulatory Affairs, and Documentation in the Medical Devices domain.Skills & Requirements:Minimum 3 years of experience in Medical Devices Regulatory Affairs, Quality Assurance, or Documentation...
-
Regulatory Affairs Associate
1 day ago
Madurai, India HCLTech Full timeExperience: 2 to 5 yearsEducation: Bachelor's degree in Biomedical, Mechanical, or B.PharmWe are looking for talented professionals for roles in Quality Assurance, Regulatory Affairs, and Documentation in the Medical Devices domain.Skills & Requirements:Minimum 3 years of experience in Medical Devices Regulatory Affairs, Quality Assurance, or Documentation...
-
Regulatory Affairs Associate
12 hours ago
Madurai, India HCLTech Full timeExperience: 2 to 5 yearsEducation: Bachelor's degree in Biomedical, Mechanical, or B.PharmWe are looking for talented professionals for roles in Quality Assurance , Regulatory Affairs , and Documentation in the Medical Devices domain.Skills & Requirements:Minimum 3 years of experience in Medical Devices Regulatory Affairs , Quality Assurance , or ...
-
Regulatory Affairs Associate
4 days ago
Madurai, India HCLTech Full timeExperience: 2 to 5 yearsEducation: Bachelor's degree in Biomedical, Mechanical, or B.PharmWe are looking for talented professionals for roles in Quality Assurance, Regulatory Affairs, and Documentation in the Medical Devices domain.Skills & Requirements:Minimum 3 years of experience in Medical Devices Regulatory Affairs, Quality Assurance, or Documentation-...
-
Regulatory Affairs Associate
3 days ago
Madurai, India HCLTech Full timeExperience: 2 to 5 yearsEducation: Bachelor's degree in Biomedical, Mechanical, or B.PharmWe are looking for talented professionals for roles in Quality Assurance, Regulatory Affairs, and Documentation in the Medical Devices domain.Skills & Requirements:Minimum 3 years of experience in Medical Devices Regulatory Affairs, Quality Assurance, or Documentation-...
-
Regulatory Affairs Associate
5 days ago
Madurai, India HCLTech Full timeExperience: 2 to 5 years Education: Bachelor's degree in Biomedical, Mechanical, or B.Pharm We are looking for talented professionals for roles in Quality Assurance, Regulatory Affairs, and Documentation in the Medical Devices domain. Skills & Requirements: Minimum 3 years of experience in Medical Devices Regulatory Affairs, Quality Assurance, or...
-
Regulatory Affairs Associate
3 days ago
Madurai, India HCLTech Full timeExperience: 2 to 5 years Education: Bachelor's degree in Biomedical, Mechanical, or B.Pharm We are looking for talented professionals for roles in Quality Assurance , Regulatory Affairs , and Documentation in the Medical Devices domain. Skills & Requirements: Minimum 3 years of experience in Medical Devices Regulatory Affairs , Quality Assurance , or...
-
Regulatory Affairs Associate
1 day ago
Madurai, India HCLTech Full timeExperience: 2 to 5 years Education: Bachelor's degree in Biomedical, Mechanical, or B.Pharm We are looking for talented professionals for roles in Quality Assurance , Regulatory Affairs , and Documentation in the Medical Devices domain. Skills & Requirements: Minimum 3 years of experience in Medical Devices Regulatory Affairs , Quality Assurance , or...
-
Regulatory Affairs Associate
2 weeks ago
Madurai, Tamil Nadu, India HCLTech Full time ₹ 6,00,000 - ₹ 8,00,000 per yearPreferred candidate profileQualifications/ JD:Bachelor's degree in Mechanical / Biomedical / SW /HW Engineering, Quality Assurance, Regulatory Affairs, or a related field.In-depth understanding of medical device regulations, including FDA 21 CFR Part and ISO 13485:2016 requirements for design controls and DHF.Experience with risk management principles (e.g.,...
