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Regulatory Affairs Specialist 
(Job)

adzuna-us  |  United States  |  

Ref:
ADZUNA-US-DN2F8
Direct:
Employer:
Location:
United StatesProcter & Gamble Plaza, OH, 45202
Category:
Information Technology/Computing
Work Type:
Permanent
Work Time:
Full Time
Tags:
job,united-states,adzuna

Description 

The candidate will work with client Client teams to deliver best in-class solutions for regulatory submissions.

Assist in the creation of technical documentation (technical files and design dossiers) for Spine products that will meet the requirements of the new Medical Device Regulation (MDR) in the European Union.

Strong knowledge of EU Medical Device regulations and guidance documents as well as relevant standards.

Experience of Tech File and technical Documentation for submission to notified bodies Ability to work with cross-functional team members including (but not limited to) RD, Quality, Labelling, Sterility, Medical and Clinical.

Experience in working with PLM systems (i.e.

Agile and Windchill) Proficient with MS Office applications such as MS Word, PowerPoint, Excel.

Excellent communication and inter-personal skills.

Ability to manage multiple tasks and be detail-oriented.

Experience in coordinating with offshore teams, preferably experience of working with teams in India Responsibilities Identify reference documents for technical documentation including, but not limited to design and risk documents, verificationvalidation documents, standards conformance, and labeling.

Identify and adhere to policies, procedures and work instructions which support technical documentation activities.

Provide support for Clinical Evaluation Reports including references to required documentation.

Align technical documentation according to OneMD technical documentation structure proposed by the MDR team.

Prepare technical documentation for submission to and reviewed by Notified Bodies, as required.

Facilitate worldwide product registration activities by compiling appropriate dossiers, submissions and responses to regulatory bodies.

Maintain information on worldwide regulatory requirements and the status of product registrations.

Be responsible for adherence to timelines and ensure milestones are achieved.

Report issues to the Customer and Client management to ensure appropriate closure.

Qualifications BS Years of experience required for position 4-10