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Cook Group

Medical devices for minimally invasive care

Regulatory Affairs Specialist 1

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBloomington, IN, USANo salary listed

About the Job

Requirements

  • An associate degree in Regulatory Affairs, or experience of such kind and amount as to provide a comparable background; a bachelor's degree in a related field is preferred.
  • Proficient in reading, writing, and speaking English.
  • Must be legally authorized to be employed in the United States.
  • Must be able to perform the essential functions of the job, subject to reasonable accommodation requirements under the ADA.
  • Must maintain all training requirements for the position.
  • Must work and interact effectively and professionally with others throughout various levels of the global organization.
  • Must strictly adhere to safety requirements.
  • Must maintain regular and punctual attendance.
  • Must maintain company quality and quantity standards.
  • Must have effective communication skills and be able to work collaboratively and independently with minimal supervision.
  • Ability to remain calm and receptive in fast-paced situations.

Responsibilities

  • Plan and prepare submissions to obtain regulatory approvals for new and modified Class I, II, III, and IV medical devices in specific markets.
  • 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 Regulatory Specialist and Regulatory Science team leaders, and assist with regulatory strategies.
  • Prepare regulatory submissions for new products, product changes, and re-registrations for specific regions.
  • Maintain registration information, including license numbers and expiration dates, and obtain re-registration approvals before license expirations to prevent 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 collection of clinical data.
  • Support currently marketed products as necessary, including providing input on change requests.
  • Maintain and organize regulatory records to demonstrate compliance with applicable regulations.
  • Communicate and interface directly with regulatory authorities to ensure timely product approvals.
  • Adhere to the Quality Management System and its processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements.
  • Travel internationally and domestically as required.

Desired Qualifications

  • A bachelor's degree in a related field.

About the Company

Cook Group

Medical devices for minimally invasive care

Cook Group manufactures medical devices focused on minimally invasive procedures. Its Cook Medical division develops and produces a broad portfolio—over 16,000 products—across cardiology, urology, gastroenterology, endoscopy, and vascular care. The company sells to hospitals and clinics worldwide, operating a B2B model in about 135 countries, with a European footprint centered in Ireland. As a family-owned business led by Carl Cook, it aims to support clinicians with reliable technologies and clinical support to expand alternatives to open surgery.

Company size
5,001-10,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Paris, France
Founded
1963

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