Regulatory Consultant

About the job

Key Responsibilities

1. Provide strategic regulatory guidance and support to clients, primarily manufacturers of medical devices and IVD devices

1. Prepare, review, and manage regulatory submissions and documentation for local and international markets

1. Coordinate with regulatory authorities and respond to regulatory queries effectively

1. Support clients in achieving and maintaining regulatory compliance

1. Monitor changes in regulatory requirements and provide timely recommendations

Why Join Neujin?

1. Opportunity to work with leading medical device and IVD manufacturers

1. Exposure to global regulatory frameworks and international markets

1. Collaborative and growth-oriented work environment

1. Continuous learning and career development opportunities

Skill(s) required

Medical Writing Quality Assurance/Quality Control (QA/QC)

Who can apply

Only those candidates can apply who

1. have minimum 1 years of experience

Other requirements

Qualifications:

1. Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Biotechnology, or a related field

1. 3–5 years of relevant experience in Regulatory Affairs (RA), Quality Assurance (QA), or Design within medical device or IVD manufacturing companies