[ref. r47439917] View Jobs Description - Raritan
We're disrupting outdated healthcare ecosystems and infusing them with transformative ideas to help people thrive throughout every stage of their lives. With a reach of more than a billion people every day, there’s no limit to the impact you can make here.
Are you ready to reimagine healthcare?
Regulatory affairs (RA) is a profession developed from the desire of governments to protect public health by controlling the safety and efficacy of products in areas including pharmaceuticals, medical devices and consumer products among others, and by the companies responsible for the discovery, testing, manufacture and marketing of these products wanting to ensure that they supply products that are safe and make a worthwhile contribution to public health and welfare.
Position SummaryThe Med Tech Global RA Co Op role will provide an opportunity to develop practical experience in one or multiple areas.Med Tech Global RA Co Op Experiences Include:
- Assist in the compilation of requirements for global regulatory submissions of our products.
- Support the acquisition and management of files to meet applicable regulations.
- Attend project team meetings with RA lead to assist in strategic discussions to hone team collaboration skillset.
- Learn regulatory affairs competencies to ensure product registration lifecycle processes compliance.
- Evaluate current processes and propose opportunities for efficiencies/improvements.
- Data analytics from regulatory information management systems (RIM) and reports/ dashboards /presentations development.
- US and Global Regulatory Policies Understanding and Shaping activities.
Qualifications
Currently enrolled full-time and have completed at least 2 years in an undergraduate program, or enrolled full-time in a graduate program (M.S., M.E., Ph.D. or M.D.)- Pursuing a degree majoring in a scientific, technology, engineering, business or law related field. - Examples include, biomedical, biochemical, civil, mechanical, or electrical engineering, data analytics/applied statistics, quantitative modeling in biology, pharmacy, pharmaceutical sciences, life sciences, medical / scientific writing or public health administration.
- Candidate must be legally authorized to work in the United States and not require sponsorship for employment visa status (e.g., H1-B status) now or in the future.
- Available to work full-time (40 hours per week) during Spring (January-May).
- Problem-solving and time management skills
- Developing graphic communications for data and research
- Ability to work independently with direction and the confidence to seek guidance when needed•Experience within a healthcare setting or industry association
- Experience and familiarity with medical product industry and regulations
- Proficiency with productivity tools including TEAMS and Share Point
- Proficiency with Office 365
- Handle confidential information in a professional and discrete manner
Please contact us to request accommodation.Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.