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Regulatory Affairs

Regulatory Affairs & Compliance Manage and coordinate regulatory submissions certifications registrations permits licenses and other regulatory requirements relevant to Bosch products and business activities.Provide regulatory guidance to BUs and ensure timely approvals renewals and compliance.Coord...

17 days ago
Full Time

Clinical Operations Manager

Job DescriptionClinical Operations ManagerBrief Description of PositionThis role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations internal policies and procedures quality standards and adverse event reporting require...

19 days ago
Full Time

Senior Advance Quality Engineer

Work Flexibility: HybridWhat you will do- Serve as the Quality representative on New Product Development (NPD) and sustenance engineering projects.Defining the quality and compliance requirements for development of SaMD and ensuring the requirements are communicated to the stakeholders and met.Devel...

30+ days ago
Full Time

Staff Clinical Evaluation Specialist

Work Flexibility: Not availableWhat you will do- Drive the establishment of a coherent Clinical evidence strategy plan throughout the new product development cycle and ensure alignment with adjacent complex processes (Marketing strategy and claim regulatory strategy research strategy)Prepare clinica...

30+ days ago
Full Time

Senior Regulatory Affairs Specialist

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain restore health and extend life. Our 95000 employees work across more than 150 countries to put patients first developing innovative medical technologies that improve the lives...

30+ days ago
Full Time

Regional Associate, Quality And Regulatory Affairs...

Dealing with lifecycle management of pharmaceutical product and medical devices in Asia Pacific Markets including administrative and CMC variations Labelling Safety updates and Annual reports.Work with Country LRA Cluster Hub Global CDRA labelling team for strategy preparation and implementation for...

30+ days ago
Full Time

Product Stewardship & Regulatory System Specialist

Product Stewardship & Regulatory System Specialist Reports To: Product Stewardship and Regulatory SupervisorDepartment: Product Stewardship and Regulatory AffairsLocation: Gurugram IndiaGeneral DescriptionThe Product Stewardship & Regulatory Affairs (PSRA) Specialist supports the companys compliance...

30+ days ago
Full Time

Product Stewardship & Regulatory Specialist Cb3 Nm

Product Stewardship & Regulatory Specialist - CB3 - NM Reports To: Product Stewardship and Regulatory SupervisorDepartment: Product Stewardship and Regulatory AffairsLocation: Gurgaon IndiaGeneral DescriptionThe Product Stewardship & Regulatory Specialist supports the companys compliance with global...

30+ days ago
Full Time

Staff Regulatory Specialist- Post Market Intellige...

Work Flexibility: HybridWhat you will do-Perform adverse event assessment and regulatory reporting activities for medical devices in accordance with applicable global regulatory requirements.Review and evaluate product complaints and post-market information to determine reportability regulatory time...

30+ days ago
Full Time

Senior Regulatory Affairs Specialist

DescriptionSupport new product registrations and license renewals for medical device and fertility products in India Sri Lanka and Nepal ensuring compliance with applicable local regulatory requirements. Act as the primary regulatory liaison with external consultants distributors and local health au...

30+ days ago
Full Time

Ra Senior Specialist (regulatory Affairs)

This is whereyour work makes a difference.At Baxter we believe every personregardless of who they are or where they are fromdeserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater...

30+ days ago
Full Time

Regulatory And Quality Specialist

Would you like to join an international team working to improve the future of healthcare Do you want to enhance the lives of millions of people Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in p...

30+ days ago
Full Time

Senior Engineer, Gpe Lifecyle Management

Work Flexibility: HybridWhat You Will Do / Roles & ResponsibilitiesAs a member of the Global Product Engineering team you will gain in depth knowledge about Strykers Trauma & Extremities portfolio. You will learn how Bone Plates & Screws External Fixators Surgical Instruments and many other products...

30+ days ago
Full Time

Lead Government Relations, India

Location:Gurugram Haryana IndiaJob ID: R0142307Date Posted:Company Name:HITACHI ENERGY INDIA LIMITEDProfession (Job Category):Communications & Corporate AffairsJob Schedule:Full timeRemote:NoJob Description:About Hitachi EnergyHitachi Energy is a global leader in electrification powering the electri...

30+ days ago
Full Time

Senior Regulatory Affairs Manager, India & South A...

Job Description SummaryProvides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launch premarket submissions/registrations and postmarket compliance working closely with healthcare regulatory bodies globally. Has knowledge of best p...

30+ days ago
Full Time

Senior Advanced Quality Engineer

Work Flexibility: HybridWhat you will do-Support New Product Development (NPD) Design Quality Engineering activities for orthopedic medical devices with a primary focus on risk management usability engineering and design control as per the project and business need.Effectively collaborate with cross...

30+ days ago
Full Time

Clinical Trial Coordinator

Job DescriptionClinical Trial CoordinatorUnder the oversight of the line-manager this role is responsible for comprehensive trial and site administration and involves preparing collating distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management...

30+ days ago
Full Time

Clinical Trial Coordinator

Job DescriptionClinical Trial CoordinatorUnder the oversight of the line-manager this role is responsible for comprehensive trial and site administration and involves preparing collating distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management...

30+ days ago
Full Time

Assistant Manager Regulatory Affairs

Our client is looking for an Assistant Manager - Regulatory Affairs to monitor interpret and ensure compliance with automotive regulations coordinate product certification and homologation and act as the liaison between engineering teams certification bodies and regulatory authorities. Mandatory Req...

30+ days ago
Full Time

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