bengaluru karnataka regulatory affairs remote Jobs – 11 Open Jobs Today

Staff Regulatory Affairs - Bangalore
Beckman Coulter Life Sciences —Bengaluru, Karnataka
- Full-time
- Remote
- Master's degree
- Project management
- AI
- Paid time off
- Work from home
Specialist - Regulatory Affairs - Operations 4A
Genpact India Pvt. Ltd. —Bengaluru, Karnataka
- Full-time
- Hybrid work
- Data analysis skills
- English
- Master's degree
Quick apply
14d
Global Regulatory Lead Partner
Syner-G —Bengaluru, Karnataka
- Remote
- Analysis skills
- Project management
- Bachelor's degree
Quick apply
Product Compliance Specialist III
Thermo Fisher Scientific —Bengaluru, Karnataka
- Full-time
- B.Sc
- Master's degree
- Project management
Supervisor, Product Compliance
Thermo Fisher Scientific —Bengaluru, Karnataka
- Full-time
- B.Sc
- Master's degree
- Project management
Head of Clinical Education - APAC
Dexcom —Bengaluru, Karnataka
- Full-time
- Medicine
- Up to 50% travel
- English
Senior Medical Writer
Healthminds Consulting —Bengaluru, Karnataka
- Full-time
- Medicine
- Doctoral degree
- Writing skills
- Health insurance
Webinar Expert
Astellas —Bengaluru, Karnataka
- Hybrid work
- Marketing
- English
- Project management
- Work from home
Global Classification Senior Specialist
Cytiva —Bengaluru, Karnataka
- Full-time
- Remote
- Microsoft Excel
- Engineering
- Windows
- Paid time off
- Work from home
Clinical Marketing Manager
Intuitive Surgical —Bengaluru, Karnataka
- Sales
- Master's degree
- Project management
7d
Senior Group Manager - Product Marketing
Intuitive Surgical —Bengaluru, Karnataka
- Up to 50% travel
- Master's degree
- Analysis skills
7d

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Specialist - Regulatory Affairs - Operations 4A
Genpact India Pvt. Ltd. —Bengaluru, Karnataka
Responsibilities: Research and stay updated on regulations relevant to the industry. Provide guidance and training to staff on compliance matters.
Quick apply
14d

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Staff Regulatory Affairs - Bangalore

Beckman Coulter Life Sciences -
Bengaluru, Karnataka

Apply Now

Job details

Full-time

Benefits

Paid time off
Work from home

Qualifications

Master's degree
Project management
AI
FDA regulations

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.

Apply Now

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regulatory affairs remote jobs in bengaluru karnataka

Staff Regulatory Affairs - Bangalore

Specialist - Regulatory Affairs - Operations 4A

Global Regulatory Lead Partner

Product Compliance Specialist III

Supervisor, Product Compliance

Head of Clinical Education - APAC

Senior Medical Writer

Webinar Expert

Global Classification Senior Specialist

Clinical Marketing Manager

Senior Group Manager - Product Marketing

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