Regulatory Affairs Jobs | Phillips Medisize is Hiring | Apply Now
Ready to advance your career in global regulatory compliance? Phillips Medisize, a Koch company, is hiring a Regulatory Affairs Specialist in Bangalore. This role is ideal for professionals seeking impactful Regulatory Affairs jobs at the intersection of medical devices and drug regulations. Join a global team and grow within a trusted Koch career ecosystem while building long-term success in high-value life science jobs.
Job Details
- Job Title: Regulatory Affairs Specialist
- Location: Bangalore, Karnataka
- Career Field: Quality
- Job Number: 180901
About the Company
Phillips Medisize is a leading global provider of medical device and drug delivery solutions and is part of Koch Industries. The company supports innovation across medical devices, diagnostics, and pharmaceutical delivery systems. With strong global regulatory expertise, Phillips Medisize works closely with R&D and quality teams worldwide. The organization emphasizes compliance, innovation, and patient safety. It offers structured growth within a broader Koch career framework. Phillips Medisize provides stable and rewarding life science jobs.
Key Responsibilities
- Maintain a deep understanding of country-specific regulatory requirements.
- Execute regulatory strategy by generating country-specific regulatory documentation.
- Work in close cooperation with the project manager and the regulatory team.
- Identify and interface with local representatives worldwide.
- Review and ensure compliance of the technical documentation.
- Assemble regulatory submission packages.
- Submit required documentation to gain market clearance.
- Interact with customers and regulatory authorities to ensure regulatory clearance.
- Support development and improvement of the regulatory affairs & submission process.
- Maintain market clearance and assess change impact on approval status.
Education
Bachelor’s degree in life science, engineering or equivalent.
Skills
- Proven experience in regulatory within the medical device / pharmaceutical industry.
- Experience in preparing technical documentation intended to be used for submission.
- Willingness, and ability to quickly acquire new knowledge.
- Systematic, rigorous, and structured thinking and documentation.
- Strong organizational skills, and the ability for multi-tasking.
- Pro-activity, self-drive, and goal-oriented.
- Ability to work in an evolving, challenging, and multi-disciplinary environment.
- Excellent written and verbal communication skills in English.
- Proficiency with MS Office.
The Regulatory Affairs Specialist role at Phillips Medisize offers a strong opportunity to work in a complex global regulatory environment. Backed by the stability and values of a Koch career, this position stands out among life science jobs for professionals seeking growth, global exposure, and long-term impact in Regulatory Affairs jobs.
