Regulatory Affairs Specialist

Job Title: Regulatory Affairs SpecialistLocation: Bengaluru, Karnataka, IndiaContract Type: Full-timeSeniority Level: Mid-Senior levelAbout the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Lifelancer. In this role, you will be responsible for ensuring compliance with various food regulations and laws in...

Job SummaryWelcome to Dozee, a pioneering healthcare company seeking a seasoned Regulatory Affairs Specialist to spearhead our medical device compliance efforts. This is an exceptional opportunity for a highly motivated individual with expertise in navigating the complex landscape of medical device regulations.About the RoleWe are looking for a seasoned...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Dozee. As a key member of our Quality Assurance department, you will play a critical role in ensuring the compliance of our medical devices with regulatory requirements.About the RoleThis is a fantastic opportunity for an experienced professional to leverage...

About the OpportunityGainwell Technologies is a leading technology company that values innovation and excellence. We are seeking a Regulatory Affairs Specialist to join our team and play a critical role in ensuring compliance with regulatory requirements.Key ResponsibilitiesDevelop and update compliance policies and procedures.Disseminate regulations to...

**Job Summary:**We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Dozee. This role will be responsible for ensuring compliance with local and international regulations, including US FDA, EU MDR, and ISO 13485.The ideal candidate will have a strong understanding of medical device regulations, experience with international...

Job Title: Regulatory Affairs Specialist for Medical DevicesLocation: Bengaluru, Karnataka, IndiaContract Type: Full-timeSeniority Level: Mid-Senior levelLifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. We connect talented professionals with opportunities in pharma, biotech, health sciences, healthtech and IT domains.Estimated Salary:...

About the RoleWe are seeking a skilled Regulatory Affairs Specialist to join our team at Biocon. In this role, you will be responsible for preparing and reviewing regulatory documents, including ANDA submissions in the US market.Key Responsibilities:Document Preparation and Review: Prepare, review, and submit high-quality regulatory documents, such as ANDA...

Job Overview: We are seeking an experienced Compliance Officer to join our team at Avenue Code. The ideal candidate will have a strong background in compliance, risk management, and regulatory affairs. This is a full-time position with a competitive salary of $120,000 per year.

Job SummaryWe are seeking a seasoned Senior Regulatory Affairs Specialist to join our dynamic team at AliveCor. As a key member of the regulatory team, you will play a crucial role in overseeing medical device development and market introduction worldwide.Your primary responsibility will be to manage product submissions, perform regulatory pre- and...

Job Title: Regulatory Affairs SpecialistAt Biocon, we are seeking a highly skilled Regulatory Affairs Specialist to join our team. This role will be responsible for ensuring compliance with regulatory requirements and guidelines in the US market.Key Responsibilities:Preparation and Submission of ANDA/ANDS: Hands-on experience in preparing, reviewing, and...

At Biocon, we are seeking an experienced Regulatory Affairs Specialist to join our team and contribute to the development of pharmaceutical products.Job DescriptionKey Responsibilities:We require a skilled professional to prepare, review, and submit ANDA applications for US market approval in a timely manner.The selected candidate will be responsible for...

Job SummaryWe are seeking a seasoned Regulatory Affairs Specialist to join our team at Biocon. As a key member of our formulation and submissions team, you will be responsible for preparing, reviewing, and submitting ANDA/ANDS in the US market, ensuring compliance with regulatory guidelines.The ideal candidate will have hands-on experience with life cycle...

Job Description: As a key member of the MTC Group team, you will be responsible for ensuring the company's compliance with all applicable laws and regulations. Your expertise will be instrumental in maintaining a positive relationship between the company and government departments.Responsibilities:Serve as the primary point of contact between the company and...

About the RoleWe are seeking an experienced Medical Regulatory Affairs Lead to join our team at Bioplus Life Sciences. As a key member of our Medical Affairs team, you will play a crucial role in ensuring compliance with regulatory requirements from various regions (FDA, EU, MHRA, and others) for activities supported.As a seasoned professional in medical...

Lifelancer is a talent-hiring platform connecting professionals with opportunities in life sciences, pharma, and IT.Join us as a Regulatory Affairs Professional to ensure compliance with international regulations for medical devices.We are looking for a skilled professional with 6-10 years of experience in regulatory affairs for Software as Medical Device,...

Job Title:Assistant Manager - Regulatory AffairsCompany Overview:Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT.Estimated Salary:$90,000 - $110,000 per annumJob Description:We are seeking an experienced Regulatory Affairs Professional to join our team at Lifelancer. As a key member of our regulatory affairs department, you will be...

Job OverviewWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at AliveCor, a pioneering healthcare company dedicated to empowering individuals to take control of their heart health.The successful candidate will play a crucial role in ensuring the compliance and regulatory readiness of our medical devices, working closely with...

About Celegence LLC:As a leading provider of regulatory affairs services, we help life science organizations ensure compliance with global regulations and deliver exceptional patient value.Company Overview:Celegence is a privately owned business based in Chicago, IL, with offices in the U.K. and Bangalore. We offer consulting, services, and solutions to...

Job Description:As a Medical Device Regulatory Affairs Specialist at Dozee, you will play a pivotal role in ensuring the company's products meet regulatory requirements. Your primary responsibility will be to plan, establish, and maintain a Quality Management System (QMS) in accordance with EN ISO 13485. This involves implementing regulatory strategies for...

As a Regulatory Affairs Specialist with Biocon, you will be responsible for preparing and reviewing ANDA/ANDS applications for the US market. This role requires a deep understanding of life cycle management for products filed in the US market.About the RoleThe ideal candidate will have hands-on experience with preparation, review, and submission of ANDA/ANDS...