Medical Affairs

Medical Affairs **Job Overview**: As an Medical affairs, you will play a pivotal role in supporting the marketing and sales teams with scientific expertise. You will collaborate across functions to ensure the accuracy and scientific integrity of marketing materials, product launches, and ongoing brand management. This role requires a deep understanding of...

Company OverviewOMC Medical Limited is a healthcare company based in the UK, specializing in UK MHRA Registration, European Authorized Representation, global product registrations, and other regulatory services.Salary £40,000 - £60,000 per annum, depending on experience.Job DescriptionThis is a full-time, remote-based role for a Regulatory Affairs Human...

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you've got big plans '“ so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix...

Company OverviewOMC Medical Limited is a UK-based healthcare company specializing in medical device regulations, Brexit customs clearance, and EUDAMED registration. We provide comprehensive solutions to the healthcare industry.SalaryThe estimated salary for this role is £30,000 - £40,000 per annum, depending on experience.Job DescriptionThis is a full-time...

Primary Responsibilities Partner closely with internal stakeholders such as commercial (marketing and sales), regulatory, Medical Information, Drug safety, Clinical development, legal, compliance and other BU medical affairs teams to develop, lead and execute an integrated set of medical plans in alignment with commercial for supporting the allocated...

Company Description OMC Medical Limited is a healthcare company based in UK, specializing in UK MHRA Registration, European Authorised Representation, global product registrations, and other regulatory services. We provide services such as Brexit customs clearance, EUDAMED registration, and software as a medical device (SaMD) registration, offering...

Job Description: - Responsible for writing clinical evaluation reports. - Able to interpret, analyse and draw conclusions from the clinical data obtained from clinical trials, literature, etc. - Responsible for preparing software documentation - Responsible for preparing technical documentation for regulatory compliance (EU MDR, CDSCO) - Responsible for...

We are seeking a highly skilled Regulatory Affairs professional to lead our medical device regulatory strategy and submission processes.Job OverviewG&L Healthcare Advisors is a leading consulting firm in the medical device industry, providing expert guidance and support to clients worldwide.Estimated Salary: $120,000 - $180,000 per yearAbout the RoleThis...

Key Job DetailsJob Title: Regulatory Affairs Professional for Medical DevicesLocation: Flexible working arrangements (remote/hybrid)Estimated Salary: £85,000 - £105,000 per annumAbout the RoleWe are seeking a highly experienced Regulatory Affairs professional to join our international team at G&L Healthcare Advisors. As a key member of our team, you will...

ABOUT THE COMPANY THE OPPORTUNITY As a Medical Advisor at J&J Innovative Medicine India, you will play a key role in leading and shaping one of the Oncology Portfolio strategy closely in collaboration with cross functional team, developing and executing strategic robust and innovative medical plans with impact, leading and developing targeted evidence...

A regulatory affairs (RA) professional in the in vitro diagnostics (IVD) industry typically has responsibilities that include: - **Developing regulatory strategies**: Creating and implementing global regulatory strategies for IVD products - **Reviewing submissions**: Reviewing and revising submissions to regulatory agencies - **Managing change control**:...

**JOB TITLE: Medical Advisor For Nutraceuticals Division** **Job description**: - MBBS with M.D. Pharmacology/Medicine or full time post-graduate qualification in any discipline of medicine Experience: 2- 4 yrs **Role and Responsibilities** - Core scientific member of cross-functional franchise team and a disease area expert, responsible for scientific...

**Company Description** Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because **Good Health Can’t Wait**. We started in 1984 with a modest...

**Company Description** RESPONSIBILITIES: **2. **Serve as a point of contact within the Medical Affairs team for external experts within an assigned geographic area in order to satisfy their needs for scientific knowledge in assigned therapeutic area and, when requested, relevant AbbVie medicines, to support their safe, effective and appropriate use. **3....

Responsibilities High clinical quality in the Company’s programs and improvement in outcomes of patients participating in the programs Serve as professional anchor for the registration as Clinical Establishment including liaison with patient’s doctors where needed Primary Execute ongoing oversight on patient reviews by Clinical Pharmacists to ensure...

VACANCY REGULATORY AFFAIRS EXECUTIVE (Pharma Company is manufacturing veterinary products) Job Location: Mumbai Maharashtra Eligibility: - M. Sc / B. Sc / M. Pharm / B. Pharm. Degree / Diploma in Regulatory Affairs. - Should have good knowledge of preparing registration of Drugs & Feed Supplements in different countries - Minimum 2 years experience in...

Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 125 years. We embrace research and science - bringing creative ideas, products and services to advance the health and well-being of people. Every day, our more than 130,000 employees across the world are blending heart, science and ingenuity to...

Regulatory affairs officers ensure that products such as foods, cosmetics, pharmaceuticals and veterinary medicines - and the steps involved in developing, testing and marketing them - meet legislative requirements. **Typical duties include**: - studying scientific and legal documents to check they meet legal requirements. - gathering, evaluating,...

**Key Responsibilities**: - Manage regulatory submissions for Class 1 medical devices in India. - Ensure compliance with Indian medical device regulations (MDR). - Maintain regulatory documentation and support product registration processes. - Liaise with regulatory bodies for approvals and updates. **Qualifications**: - Proven experience in regulatory...

Provide scientific expertise, build knowledge and activity based relationships with Key Opinion Leaders to advance medical practice and research for the benefit of the society, thus enhancing Pfizer’s image in the scientific community. - To actively contribute to the organization/business by taking responsibility for the scientific, technical and ethical...