Medical Affairs Strategist

Medical Content StrategistWe are seeking a skilled Medical Content Strategist to join our team. As a key member of our medical communications group, you will be responsible for developing high-quality scientific, medical, and educational materials.This role involves creating engaging content for various audiences, including healthcare professionals,...

Job Overview:The General Manager of Medical Affairs will lead the strategic development of medical affairs at a multinational pharmaceutical company, focusing on providing robust medico-marketing support and facilitating collaboration between the medical and marketing teams. This role encompasses the creation of medical materials, training programs, and...

Medical Device Regulatory SpecialistWe are seeking a seasoned professional with extensive experience in medical devices, including quality management and regulatory affairs.About the Role:• Assess and audit medical devices to ensure compliance with ISO 13485, MDD 93/42/EEC, Indian Medical Device Regulations, and MDR 2017/745.• Develop and implement risk...

Job Title: Medical Device Quality Assurance SpecialistIn this role, you will have the opportunity to establish and lead Design Quality Control, Assurance, and Regulatory Affairs teams within a regulated industry.The ideal candidate will have experience in developing and implementing quality management systems for medical devices, ensuring regulatory...

Your Opportunity CSL Behring is a global leader in biopharmaceuticals, dedicated to saving lives and improving the quality of life for people with rare and serious diseases. Our commitment to innovation, collaboration, and patient focus drives us to deliver superior performance and integrity in everything we do. We are looking for a Medical Science Liaison...

Medical Devices SpecialistWe are seeking a highly skilled Medical Devices Specialist to join our team. As a key member of our engineering department, you will be responsible for ensuring the quality and safety of medical devices.Main Responsibilities:Lead a team of engineers in the development, testing, and certification of medical devices.Ensure compliance...

Job Overview:We are seeking a seasoned Regulatory Affairs professional with expertise in pharmaceutical and medical device regulatory compliance. The role involves preparing, reviewing, and submitting regulatory documentation to global health authorities.Key Responsibilities:Prepared, reviewed, and submitted regulatory filings, including IND, NDA, ANDA, DMF,...

About This OpportunityWe are seeking a talented Senior Medical Writer to join our team. As a key member of our medical communications group, you will be responsible for developing high-quality scientific and educational materials that meet the needs of our clients.You will work closely with our scientific leads to develop client-ready materials such as...

About the RoleThis is a critical role in our organization, responsible for navigating the regulatory environment and ensuring alignment with business goals within India's policy framework.Key ResponsibilitiesProvide strategic direction and guidance on policy strategies that align with business objectives.Represent the company's interests with regulatory...

Regulatory Data CoordinatorAbout the JobThis role is a key position in monitoring and analyzing global regulatory trends within the life sciences industry. You will support our team by actively participating in data acquisition, surveillance, and analysis activities.You will work closely with cross-functional teams to identify emerging trends in the...