Overview
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function
Career Programs
Job Sub Function
Non-LDP Intern/Co-Op
Job Category
Career Program
All Job Posting Locations
Leeds, West Yorkshire, United Kingdom
Job Description
Duration: 12 months
Sectors and locations: Leeds
Medical Devices - Leeds (DePuy Synthes)
Position summary
Today\'s changing healthcare environment presents many exciting challenges for Regulatory Affairs (RA) professionals. RA professionals within DePuy Synthes have opportunities to participate in high-level forums that connect government agencies and industry leaders to shape a complex policy ecosystem.
They are passionate about protecting our customers while ensuring that our business complies with all product-related regulations. RA professionals are involved in all stages of the product lifecycle, so they have numerous opportunities to contribute innovative ideas, product improvements, and service models that advance the health and well-being of patients and consumers. And because they have such a broad perspective on our business activities and product lifecycles, RA professionals find many opportunities to move their careers in a direction that aligns with their individual interests and passions.
As a RA placement student you will be responsible for ensuring effective management of worldwide product registration activities to ensure that registrations are conducted in a timely manner in accordance with regulatory and company requirements.
Main duties and responsibilities
- Liaise with internal departments and worldwide regulatory colleagues to support registration activities
- Facilitate worldwide product registration activities by compiling regulatory submissions and requested documentation to worldwide regulatory affiliates
- Coordinate activities for legalization of regulatory documents
- Maintain regulatory and registration databases, including archiving, purchase requisitions and control of standards, and analyze data to provide reports to immediate manager as required
- Responsible for ensuring compliance with all local, national, international and company regulations, policies and procedures for Health, Safety and Environmental compliance to enable the site to achieve and maintain excellent results
Qualifications
- 2 years of degree level study completed
- A minimum of 2:1 achieved in first year of study
- Scientific degree type is preferable
Key skills and competencies
- Excellent planning and organizational skills
- Communication - listener, learner and thinker
- Thorough and flexible
- Cross-culturally aware
- Team player
- Enthusiastic and committed
- Excellent knowledge of Microsoft office PC packages
- Excellent written and verbal reasoning skills
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