Regulatory Affairs Specialist IV

Responsibilities The incumbent possesses knowledge of regulatory requirements gained through experience and is able to perform the essential duties and responsibilities with some direct supervision.
Domestic and international travel may be required up to 25% of time.
1. Prepare global regulatory submissions such as; 510(k), PMA, for new and modified devices.
2. Work closely with teams to develop regulatory strategies, testing requirements and other documentation to assure that regulatory submissions are prepared and approved to meet the Company s product launch timelines in US market.
3. Communicate with FDA regarding submissions.
4. Maintain a working knowledge of existing and proposed regulations, standards and guidance documents, internal procedures, and facility registration, device listing and import/export requirements.
5. Review package inserts (labeling) and promotional materials to insure compliance with FDA requirements.
1. Development of departmental and corporate Standard Operating Procedures and departmental procedures, when necessary.
2. Assist in the development of project specific and departmental budgets.
3. Represent Company in industry associations, standards organizations, and corporate regulatory/clinical group meetings.
4. Other duties as assigned.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Experience & Knowledge Essential EDUCATION and/or EXPERIENCE:
Bachelor s or Master s degree in Engineering or life sciences preferred, but other degrees may be considered.
The candidate should have a minimum of 5 years of regulatory submissions experience in the medical device industry specifically with US FDA submissions. Wound, and reconstructive device experience is desired.
Extensive knowledge of FDA regulations required.
Excellent English written and verbal communication skills including presentation skills, Microsoft Office application skills, self motivated, attention to detail, able to prioritize and manage multiple projects. Able to lead projects with minimal supervision.
Ability to read, analyze, and interpret regulations, technical standards, guidance documents, test reports, clinical and medical terminology and complex documents.
Ability to respond to inquiries and complaints from customers and regulatory agencies.
Ability to write detailed technical regulatory submissions, reports and business correspondence.
Ability to effectively present information to other employees, management and regulatory agencies.
Ability to compute ratio, percent and draw and interpret raw data into graphical representations.
Ability to convert English units into metric units and vice versa.
Ability to comprehend and apply principles of algebra, statistics, calculus and mathematical operations used in various engineering and clinical analysis.
Ability to interpret a variety of instructions furnished in written, oral, diagram or schedule form. Ability to define problems, collect data, establish facts and draw valid conclusions.
Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Ability to deal with a variety of abstract and concrete variables.
The physical demands described here are representative of those that must be met by an employee to successfully perform the essentials function of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Requires sitting, talking or listening, more than 2/3 of the time. Walking or standing less than 1/3 of the time. Use of hands to use computer or write documents less than 2/3 of the time.
Ability to travel by air and motor vehicle both domestically and internationally required. Some overnight travel required. Searching for, lifting and carrying records weighing up to 25 pounds less than 1/3 of the time.
Close vision (clear at 20 inches or less) required to review documents and operate personal computers more than 2/3 of the time.
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Requires working most of the time in an office setting.

Company Description:

About Ascent:

Ascent is a leading national technology consulting and professional services firm that focuses on tactical and strategic consulting. Ascent’s fundamental business is providing staffing services to Large Enterprise clients in our core market verticals: Financial Services, Healthcare, and Life Sciences. We focus the majority of our efforts in Staff Augmentation support of Large Enterprise Clients who utilize a Vendor Management System. Ascent works as both a reliable supplier in support of programs, as well as a Strategic Advisor in support of enterprise efforts to establish best in class preferred vendor programs. Ascent was ranked in the 2007 and 2008 Inc. 500 and recognized specifically for its innovative work in staff augmentation support of Large Enterprise preferred vendor accounts.

If you are ready to propel your career to new heights… read on. We are looking for talented and dedicated colleagues to join our phenomenal team. At Ascent, we have created an environment where culture, commitment and opportunity converge to yield a truly unique place to work. We know that every employee has something important to say and that every employee is integral to our success. Where else can you walk over to a founder and talk about your ideas to help build our business and have that idea implemented in 48 hours? More importantly, we do everything we can to make sure our employees not only have great jobs, but great lives.

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