Regulatory Affairs India jobs
- Beckman Coulter Life SciencesBengaluru, Karnataka
- Paid time off
- Work from home
- Master’s degree in life sciences, engineering, or related field; advanced degree preferred.10+ years of experience in regulatory affairs or regulatory…
- ProductLife GroupRemote
- Document and track regulatory submissions and regulatory authority approval.
- Provide regulatory support to clients and associate companies.
- View all ProductLife Group jobs - Remote jobs
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- Vincit Labs PVT LTdDelhi, Delhi
- Experience in interacting with regulatory authorities and managing regulatory inspections and audits.
- Strong knowledge of regulatory affairs principles,…
- PharmanoviaMumbai, Maharashtra
- Familiarity with EU regulatory requirements, guidelines and regulatory procedures.
- Monitoring regulatory developments and communicating regulatory risks,…
- sarah visionLower Parel, Mumbai, Maharashtra
- Lifecycle Management: Monitor post-approval supplements and address regulatory agency queries.
- Compliance: Ensure all research, development, and commercial…
View similar jobs with this employerGenpact India Pvt. Ltd.Bengaluru, Karnataka- The Role demands for a publisher with demonstrated ability to execute responsibility in a highly regulated & process driven environment, the Person will be…
View similar jobs with this employerMercy For AnimalsRemote- Knowledge of central and state legislative and regulatory processes.
- Elected officials and bureaucrats to advance legislative, regulatory and campaign.
View similar jobs with this employerMercy For AnimalsRemote- Knowledge of central and state legislative and regulatory processes.
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- Vitane Pharmaceuticals Pvt LtdThane District, Maharashtra
- Cell phone reimbursement
- Provident Fund
- Lead and mentor the regulatory affairs team.
- Manage regulatory databases and documentation systems.
- Identify regulatory risks and develop mitigation strategies.
- Senores PharmaceuticalsAhmedabad, GujaratDETAILS: Experience in regulatory affairs for ROW market EXPERIENCE: 2-3 years EDUCATION: B. Pharm/ M. Pharm LOCATION: Ahmedabad, India To apply, please write…
- INFINIUM PHARMACHEM LIMITEDAnand, Gujarat
- Food provided
- Provident Fund
- Support audits and inspections by regulatory authorities.
- Ensure compliance with regulatory guidelines and filing procedures.
- Abbott LaboratoriesDelhi, Delhi
- Serves as regulatory representative to marketing, research teams and regulatory agencies.
- Serves as regulatory liaison throughout product lifecycle.
View similar jobs with this employerDIFGEN PHARMACEUTICALS PRIVATE LIMITEDKukatpally, Hyderabad, Telangana- Prior experience or coursework in regulatory affairs or the pharmaceutical industry is preferred.
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- ParexelDelhi
- Understanding of regulatory documentation and compliance standards.
- Contribute to regulatory strategy development for global and regional submissions.
- View all Parexel jobs - Delhi jobs - Regulatory Affairs Specialist jobs in Delhi
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Job Post Details
Staff Regulatory Affairs - Bangalore - job post
Job details
Job type
- Full-time
Benefits
Pulled from the full job description
- Paid time off
- Work from home
Full job description
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Beckman Coulter Life Sciences, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
At Beckman Coulter Life Sciences, we know time is the most critical facet in the laboratory today: time to get life-saving therapies to patients faster; reclaiming time by automating tedious manual workflows; and saving time spent addressing erroneous or complex results.
We are partners in time and accelerate answers to critical questions through the power of automation. We develop innovations for scientists by scientists, with many of our 3,300+ global colleagues coming from the laboratory.
It’s all part of our time-tested approach to bringing meaningful innovations at the speed of life since 1935. And we’re just beginning. Working together, let’s put our time and talents together to advance human health for tomorrow.
Learn about the Danaher Business System which makes everything possible.
The Staff Regulatory Affairs is responsible for driving compliance through Regulatory change and regulatory intelligence activities including but not limited to identification, interpretation, assessment and project management of changes. The purpose of this role is to maintain compliance with regulatory requirements on products and business systems and avoid audit observations and shipping delays.
This position reports to the Senior Manager, Regulatory Affairs and is part of the Global Quality and Regulatory affairs team and will be fully remote.
In this role, you will have the opportunity to:
- Monitor and analyze global regulatory intelligence across: IVD and medical device regulations (e.g., EU IVDR, US FDA regulations and guidance),AI/Software regulations, Chemical and environmental regulations (e.g., EU REACH, RoHS, PFAS, EPA, EU CLP requirement)
- Develop detailed assessments of regulatory changes, providing actionable insights and impact analyses for internal stakeholders. Create business cases for regulatory-driven changes, including cost, resource, and timeline impact for compliance activities.
- Support global regulatory strategy development by providing intelligence-driven recommendations. Maintain regulatory intelligence repositories, dashboards, and communication tools.
- Prepare and deliver regulatory intelligence briefings, cross-functional reports, and executive summaries.
· Leverage AI-enabled tools to automate horizon scanning and early detection of regulation changes· Lead compliance gap analyses and risk assessments to proactively identify areas of regulatory exposure and develop mitigation plans in partnership with Quality and Legal teams. Ensure alignment with internal SOPs and global regulatory standards.
The essential requirements of the job include:
- Master’s degree in life sciences, engineering, or related field; advanced degree preferred.10+ years of experience in regulatory affairs or regulatory intelligence within the IVD/medical device industry.
- Strong knowledge of global IVD regulations including FDA, EU IVDR, ISO 13485, ISO 20916, and related standards. Demonstrated experience managing regulatory compliance programs, including compliance tracking systems, and audit readiness activities.
- Experience implementing regulatory intelligence systems or digital tools.
- Experience with AI/software or chemical/environmental regulations strongly preferred
- Experience interacting with regulatory agencies or notified bodies is a plus.
It would be a plus if you also possess previous experience in:
- Previous experience in a regulatory intelligence role handling gap assessment and/or coordinating remediations
Beckman Coulter Life Sciences, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
At Beckman Coulter Life Sciences we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Life Sciences can provide.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.