Regulatory Affairs Specialist 2

Requisition ID 2023-12728
Posting Date 3 weeks ago(9/15/2023 8:57 AM)
Job Location(s)
Bloomington IN United States
Position Type
Full Time
Cook Inc - Bloomington
Regulatory Affairs


The Regulatory Affairs Specialist 2 is responsible for the planning and preparation of submissions to obtain regulatory approvals for new and modified Class I, II, III and IV medical devices in specific markets. In addition to submissions, the Regulatory Affairs Specialist will serve as a communication liaison between the Cook manufacturer and the Cook Local Office / Cook Distributor.


- Serve as a liaison on regulatory issues between the Cook manufacturer and Cook Local Office and/or Cook Distributor
- Communicate region-specific regulatory requirements to the Regulatory Specialist/Regulatory Science team leaders and assists with the regulatory strategies
- Prepare regulatory submissions for new products, product changes, and re-registrations as required for the specific regions
- Maintain registration information (license numbers, expiration dates, etc.) and obtain re-registration approvals in advance of license expirations to ensure no disruption in product availability
- Collaborate with Regulatory Scientific Affairs on all high risk devices and new technologies
- Collaborate with the Clinical Functional Unit on projects requiring the collection of clinical data
- Mentor other RA Specialists regarding technical content and processes
- Provide support to currently marketed products as necessary including input on change requests, etc.
- Maintain and organize appropriate regulatory records to demonstrate compliance with applicable regulations
- Excellent problem solving skills and ability to work in collaborative and independent work situations and environments with minimal supervision
- Must maintain all training requirements for the position, while seeking out opportunities for continuous development and growth.
- Adhere to the Quality Management System and its processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements.

- Must work and interact effectively and professionally with and for others throughout various levels of the global organization.
- Must strictly adhere to safety requirements.
- Maintain regular and punctual attendance.
- Must maintain company quality and quantity standards.
- Must have effective communication skills and ability to work in a collaborative and independent work situations and environments with
minimal supervision.
- Ability to remain calm and receptive in fast paced situations.



- Bachelor’s degree in a related field; or experience of such kind and amount as to provide a comparable background required
- 3+ years of regulatory experience required
- Regulatory Affairs Certification (RAC) preferred
- Proficient in reading, writing and speaking the English language


Physical Requirements:

- General office environment
- Sits for extended periods
- Requires close visual acuity when working with computers, etc.
- Requires occasional early morning or late evening teleconferences
- International and domestic travel as required

- Must be able to perform the essential functions of the job, subject to reasonable accommodation requirements under the ADA.


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