Regulatory Affairs Intern

internship - , paid

Zimmer Biomet
Parsippany, NJ
Closed
Posted 41 Days ago
Zimmer Biomet
Parsippany, NJ
internship - , paid
Posted 41 Days ago
Closed

Description

Regulatory Affairs Intern Zimmer Biomet - Parsippany, NJ3.7 Full-timeEstimated: $39,000 - $55,000 a year Save Skills * Computer Skills * Writing Skills * Analysis Skills * Microsoft Office Responsible for assisting the team with regulatory information. This is an educational position, providing an overview and training in Regulatory Affairs (RA). This position requires basic knowledge and understanding of medical device industry and technical concepts. May perform some or all of the following functions, depending upon their specific assigned focus. Principal Duties and Responsibilities Coordinate and assist in the preparation of technical documentation for use in regulatory submissions worldwide Assist with the research, analysis and communication of information pertaining to the appropriate regulatory pathway for new or modified products Assist in the development and review of departmental work instructions, submission templates and/or training materials Assist in the review of labeling for compliance with applicable regulations Assist in the review of advertising and promotional items Follows Zimmer Biomet RA policies and procedures Miscellaneous administrative RA responsibilities as assigned Expected Areas of Competence Strong writing and communication skills Strong interpersonal skills Versatility, flexibility, and willingness to work with changing priorities Strong organizational, problem-solving and analytical skills Affinity for details Ability to work with rapid changes Ability to learn regulations pertinent to medical devices Ability to learn basics of medical device regulations Ability to handle multiple projects and meet deadlines, working closely with RA Specialists and Managers Basic computer skills, including Microsoft Office Suite Education/Experience Requirements Actively enrolled student (at least a sophomore standing), pursuing a degree in life sciences, technical/engineering or related field, or non-US equivalent required. Other degrees may be considered. GPA of 3.0 or higher, strongly preferred Travel Requirements Up to 5% Additional Information EOE M/W/Vet/Dis Save

Skills

regulatory affairs, research, regulatory submissions, life sciences, medical device directive, regulations, regulatory filings, microsoft office, medical devices, analysis, communication, engineering, training, problem solving, writing

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