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Looking to build a strong Molex career in regulatory affairs within the medical device industry? This Regulatory Affairs Job at Molex offers life science graduates and professionals an exciting opportunity to work in a global regulatory environment, handling worldwide medical device registrations while collaborating with international teams at Molex’s Bangalore innovation center.
Job Details
- Job Title: Regulatory Affairs Specialist
- Location: Bangalore, Karnataka
- Career Field: Quality
- Job Number: 180901
About the Company
Molex, through its Phillips-Medisize division, is a global leader in medical device and drug delivery solutions. The company operates at the intersection of healthcare innovation, quality, and regulatory excellence. Its Global Innovation & Development Center in Bangalore supports worldwide regulatory submissions and lifecycle management. Molex is known for its structured regulatory processes and strong compliance culture. Working at Molex offers exposure to global markets and international regulatory authorities. This makes Molex a preferred destination for professionals seeking long-term growth in regulatory affairs.
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 a 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.
This Regulatory Affairs Job at Molex is a valuable opportunity for candidates aiming to build a stable and impactful career in regulatory affairs. With global exposure, structured learning, and strong industry relevance, this role is especially suitable for those seeking long-term growth in life science jobs within the medical device sector.
