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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)
The DePuy Synthes companies are inspired by the opportunity to help people return to living active and fulfilling lives. We deliver a broad array of orthopaedic and neurological solutions – inspired solutions that go beyond quality implants and include services, education, instruments and emerging technologies.
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 - External
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