Candidate Opportunities

Sr. Regulatory Affairs Specialist - 2019-002

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Location
Dane County, WI
Job Type
Direct Hire
Date
Apr 08, 2019
Job ID
2651903
My client is an industry leader that provides innovative life sciences solutions.
 
Provide regulatory support to ensure products comply with relevant domestic and international medical device and electrical equipment regulations. Provide regulatory guidance to cross-functional partners and demonstrate strategic thinking and creativity in support of programs. Lead the preparation and submission for regulatory approvals and act independently to identify and resolve problems. Develop and maintain required documentation to support regulated products.
 
PRIMARY FUNCTIONS:
1. Prepares robust regulatory applications to achieve departmental and organizational objectives
2. Creates, reviews and approves change records
3. Acts as a regulatory representative on core product development teams, communicates regulatory requirements and impact of regulations to the development team
4. Provides guidance and expertise
5. Acts as liaison between the Company and the various appropriate regulatory agencies, ensuring that communications on both sides are germane, specific and convey all necessary detail
6. Maintains ongoing surveillance and analysis of all pertinent domestic and international medical device regulations to ensure submission requirements world-wide are current, up-to-date and are entered into regulatory submission data base and file systems
7. Reviews device labeling and marketing materials for compliance with FDA submissions and applicable regulations.  Interfaces directly with FDA and other regulatory agencies
8. Conducts reviews of product and manufacturing changes for compliance with applicable regulations.  Reviews protocols and reports to support regulatory submissions
 
ESSENTIAL DUTIES:
1. Evaluate regulatory impact of proposed products.
2. Understand, investigate and evaluate regulatory requirements.
3. Provide regulatory guidance and assess regulatory implications for products throughout the product lifecycle.
4. Prepare regulatory applications, registrations, and submissions to authorities, e.g. FDA.
5. Maintain documentation needed to support regulated product throughout the product’s lifecycle.
6. Review and approval of product labeling (label disclaimers).
7. Review and approval of product literature as well as advertising and promotional materials for compliance to applicable regulations.
8. Facilitate risk assessments for regulated products.
9. Evaluate risks based on regulatory factors; provide options and recommendations to mitigate risk.
10. Understand and comply with ethical, legal and regulatory requirements applicable to our business.
 
DUTIES:
1. Organize, facilitate, or lead meetings to discuss review findings and planning issues.
2. Provide regulatory support for corporate branches.
3. Develop and conduct regulatory training, as needed.
4. Ability to develop concise, clear communication and presentations that contain both analysis and possible solutions. Experience in writing procedures and reviewing documents required to support regulated products.
5. Provide regulatory input for complaint investigations and product recalls.
 
QUALIFICATIONS:
1. BS degree; technical discipline preferred. Bachelor’s degree in life science, chemistry, or biochemical field.
2. Minimum of 8 – 10 years experience in the medical devices or in vitro diagnostic devices industry, including at least 4 years of regulatory affairs experience.
3. Comprehensive knowledge of applicable FDA regulations and experience with EU Directives and other international medical device regulations and submissions.
4. Experience with 510(k) applications, PMA supplements and US device regulations.
5. Proficiency in MS Word, Excel and other standard software programs.
6. Strong verbal and written communication skills with ability to effectively communicate at multiple levels in the organization and with work constructively with a broad range of people, both internally and externally, to achieve results.
7. Experience working in a broad cross-organizational business model preferred.
 
PREFERRED:
1. Regulatory Affairs Certified (RAC) certification.
2. Experience in developing EU Technical Files to support regulated product.
3. Experience in developing compliance files or submissions to support regulated product in other markets.
4. Ability to travel up to 10%.