Current jobs related to Sr. Specialist Regulatory Affairs - Bengaluru, Karnataka - Baxter

  • Sr. Demand Generation Associate

    4 months ago

    Bengaluru, Karnataka, India ANSR Global Corporation Full time

    ANSR Is hiring for Sr Demand Generation AssociateJob Overview:We are seeking a highly motivated and experienced Email Marketing Specialist & Contact Database execute to join our team. The ideal candidate will be responsible for developing and executing email marketing campaigns and managing our contact database to ensure that our email communication efforts...

  • Senior SEO Specialist

    4 months ago

    Bengaluru, Karnataka, India ANSR Global Corporation Full time

    Role: Sr. SEO SpecialistExperience: 5 Years of SEO experienceLocation: From Bangalore Office.ANSR is seeking an experienced SEO Lead to spearhead our digital presence and drive organic growth. The ideal candidate will have5 years of hands-on experience in all aspects of SEO, with a proven track record of implementing successful strategies in both B2B and B2C...

  • Sr HCP Analyst

    2 months ago

    Bengaluru, Karnataka, India Kenvue Full time

    Job Title: Health Care Professional AnalystWe are seeking a Health Care Professional Analyst to provide actionable insights and strategic recommendations that enhance our engagement with health care professionals (HCPs). In this role, you'll analyze data from multiple sources to ensure the effectiveness of our HCP-focused strategies, supporting the...

  • EH&S Data Steward

    2 months ago

    Bengaluru, Karnataka, India Leading-Biotechnology-Company Full time

    Position Summary:We are seeking an EHS Specialist to join our talented team in Bangalore. The EHS Specialist will support the Global EHS strategy for compliance and risk management in the delivery of Safety Data Sheets (SDS) and related product and chemical management information and processes. This individual will author product SDS using the SAP EHS module...

  • AVP (Invoice Payment & Invoice Validation)

    3 weeks ago

    Bengaluru, Karnataka, India MUFG Global Service Full time

    About the Role:Position Title: AVP - Invoice ManagementCorporate Title: Assistant Vice PresidentLocation: BengaluruJob ProfileMAIN PURPOSE OF THE ROLE:The Invoice Management Specialist plays a crucial role in supporting the organization's strategic HR initiatives through effective vendor and invoice management. Designed for a dynamic professional skilled...

  • AVP - Market Research

    3 weeks ago

    Bengaluru, Karnataka, India MUFG Global Service Full time

    About the Role:Position Title: Market, industry, and best practice researchCorporate Title: Assistant Vice PresidentLocation: Bengaluru Job Profile MAIN PURPOSE OF THE ROLE:This position will play a crucial role in supporting the organization's strategic HR initiatives by providing in depth market, industry, and HR practice research. This position is...

  • Regulatory Affairs Associate

    3 months ago

    Bengaluru, India Parexel Full time

    **Regulatory Affairs Associate** 2 to 5 years of experience in Regulatory Affairs-CMC, should be willing to work in EU Shifts. - To provide regulatory input on procedural and CMC documentation requirements specific to as defined by Health Authorities for assigned deliverable(s) including: - Submission delivery strategy - Review of documents - Analysis of...

  • Specialist- Regulatory Affairs

    3 months ago

    Bengaluru, India Baxter Full time

    This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in...

  • Regulatory Affairs Associate

    2 months ago

    Bengaluru, India Dozee Full time

    Job Description - Regulatory Affairs AssociateYour mission, if you choose to accept, will be :ResponsibilitiesParticipate in the development of regulatory submission and approval strategy in multiple countries.Ensure compliance with FDA, ISO 13485, MDR, and other relevant regulatory requirements.Maintain awareness and understanding of new and existing...

  • Regulatory Affairs Associate

    2 months ago

    Bengaluru, India Dozee Full time

    Job Description - Regulatory Affairs AssociateYour mission, if you choose to accept, will be :ResponsibilitiesParticipate in the development of regulatory submission and approval strategy in multiple countries.Ensure compliance with FDA, ISO 13485, MDR, and other relevant regulatory requirements.Maintain awareness and understanding of new and existing...

  • Regulatory Affairs Associate

    3 months ago

    Bengaluru, India Parexel Full time

    **_Regulatory Affairs Associate _**: **Experience: RIM**: **Relevant experience in Regulatory and should be willing to work in EU Shifts (12:00 - 9.00 PM)**: - **Experience of handling RIM tools - Veeva Vault specifically.**: - **Basic Regulatory knowledge on regulations and Health Authorities.**: - **Excellent communication skills.** **Knowledge and...

  • Regulatory Specialist

    2 days ago

    Bengaluru, India Tag Full time

    REGULATORY SPECIALISTAt Tag, we help brands stand out and sell more by delivering impactful content, at speed and scale and across channels & geographies. With over fifty years of production experience for some of the world’s biggest brands, we partner with our clients to create work that is efficient, effective and more importantly tells a story.We...

  • Regulatory Affairs

    2 weeks ago

    Bengaluru, India Recruise India Consulting Pvt Ltd Full time

    Experience: 8 to 20 YearsLocation: Bangalore OR RemoteSkills: Regulatory Affairs, Clinical trial application, Clinical Trial Regulation, CDSCO10+ yrs relevant experience in Clinical Trial Regulatory Submissions.Experience in managing clinical trial studies, playing Regulatory Leads for Global trials, and exposure to the European market.Expertise in handling...

  • Regulatory Affairs Associate

    2 weeks ago

    Bengaluru, Karnataka, India Planet Science Full time

    **About Us**: An established player in the B2B Pharma raw material space has recently launched an exciting new E-commerce platform **- CLYZO** **Position - Regulatory Affairs Associate.** An organization with a reputed history of 10+ years in the Pharma raw material industry, dealing in excipient products is looking for Regulatory Affair Executive having...

  • Regulatory Specialist

    3 weeks ago

    Bengaluru, India Tag Full time

    REGULATORY SPECIALISTAt Tag, we help brands stand out and sell more by delivering impactful content, at speed and scale and across channels & geographies. With over fifty years of production experience for some of the world’s biggest brands, we partner with our clients to create work that is efficient, effective and more importantly tells a story.We...

  • Regulatory Specialist

    1 day ago

    Bengaluru, India Tag Full time

    REGULATORY SPECIALISTAt Tag, we help brands stand out and sell more by delivering impactful content, at speed and scale and across channels & geographies. With over fifty years of production experience for some of the world’s biggest brands, we partner with our clients to create work that is efficient, effective and more importantly tells a story.We...

  • Regulatory Affairs Professional

    4 months ago

    Bengaluru, India Siemens Healthineers Full time

    **Internal Title**:Regulatory Affairs Professional **External Title**:Deputy General Manager **Position Summary** To perform regulatory tasks as applicable to SHPL products pertaining to regulating authorities like radiation safety related certification from Atomic Energy Regulatory Board (AERB) for Zone India (India, Bangladesh, Nepal, Sri Lanka &...

  • Regulatory Specialist

    3 days ago

    Bengaluru, India Tag Full time

    REGULATORY SPECIALIST At Tag, we help brands stand out and sell more by delivering impactful content, at speed and scale and across channels & geographies. With over fifty years of production experience for some of the world’s biggest brands, we partner with our clients to create work that is efficient, effective and more importantly tells a story.We...

  • Regulatory Affairs

    2 weeks ago

    Bengaluru, India Recruise India Consulting Pvt Ltd Full time

    Experience: 8 to 20 Years Location: Bangalore OR Remote Skills: Regulatory Affairs, Clinical trial application, Clinical Trial Regulation, CDSCO10+ yrs relevant experience in Clinical Trial Regulatory Submissions.Experience in managing clinical trial studies, playing Regulatory Leads for Global trials, and exposure to the European market.Expertise in...

  • Regulatory Affairs Executive

    4 months ago

    Bengaluru, India Indian Institute of Science, Bangalore Full time

    **Responsibilities**: - Work closely with Engineering team through product development process and design activities - Author/participate in the design validation and process validations, IQ, OQ, PQ. - Prepare, review risk management files and support risk management activities including hazard analysis and FMEA. - Identify relevant guidance documents,...

  • Lead - Regulatory Affairs

    4 months ago

    Bengaluru, India Indegene Full time

    Title: Lead - Regulatory Affairs Date: May 10, 2024 Location: Bangalore, KA, IN We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious and nimble. With Indegene, you gain a...

  • Sr. Electronic Submission Specialist

    2 weeks ago

    Bengaluru, India IN19 Alcon Laboratories (India) Pvt Ltd Company Full time

    Summary of the position: Alcon is looking to hire Sr. Electronic Submission Specialist whowill be responsible for providing Submission Management and Publishing support for Global Regulatory Affairs for submissions to US, Canada, and EU. Roles & Responsibilities: Veeva Vault RIM Submission Management & Publishing to support Global Regulatory...

  • Regulatory Affairs Intern

    3 months ago

    Bengaluru, India Indian Institute of Science, Bangalore Full time

    **Lab/Affiliation**:UTSAAH Lab, CPDM, Indian Institute of Science, Bangalore **Project**: Ikshana - An integrated system for adaptive stimulation treatment of urinary incontinence - (ikshanahealthcare.co.in)_ **___________________________________________________** **OPEN POSITION: Internship - Regulatory Affairs** **Desirable Qualifications**: Final year...

  • Lead Regulatory Affairs

    2 weeks ago

    Bengaluru, India Halma plc Full time

    About Halma:Halma is a global group of life-saving technology companies, driven by a clear purpose. We are an FTSE 100 company with headquarters in the UK and operations in 23 countries, including regional hubs in India, China, Brazil, and the US.Our diverse group of nearly 50 global companies specialise in market leading technologies that push the...

  • Regulatory Affairs Executive

    3 months ago

    Bengaluru, Karnataka, India Tresbien HR Consultancy Full time

    Hi Opening with a client into medical Devices at Nayandahalli Job Description Job Title: Sr. Executive - Regulatory Affairs Reporting To: RA Manager. Key responsibilities Duties: - Experience in preparation of Device master file and other documents as per CDSCO MDR-17 requirements and submission of documents in CDSCO portal. - Experience in preparation...

  • Regulatory Affairs Associate I

    4 months ago

    Bengaluru, Karnataka, India AstraZeneca Full time

    **Job Title: Regulatory Affairs Associate I** **Career Level - C** **Introduction to Role**: **Accountabilities**: As a Regulatory Affairs Associate, you will be responsible for document management, including uploading and tracking regulatory files and systems according to established AZ procedures and regulatory requirements. You will maintain...

Sr. Specialist Regulatory Affairs

3 months ago

Bengaluru, Karnataka, India Baxter Full time

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

Create and Review regulatory documentation for Drug, Device and Combination product renewals. Interact with non-regulatory support groups (i.e., manufacturing, product stability, quality, clinical, etc.) to request documentation necessary to support product renewals Track status and progress of regulatory documentation that will be used for renewals Coordinate and compile responses to regulatory authority renewal questions (under supervision) Use an electronic document management system to compile documents to support product renewals for submission to Health Authorities Answer internal queries for assigned products Maintain Database of Regulatory Requirements for renewals Knowledge of regulations Scientific knowledge Administrative and project management skills Ability to contribute to multiple projects from a regulatory affairs perspective Ability to multitask and prioritize Interpersonal and communication skills Technical system skills (e.g. word processing, spreadsheets, databases, online research) Proofreading and editing skills Ability to independently identify compliance risks and resolve or escalate as necessary