Regulatory Affairs Operations Specialist

Full Time
Northfield, IL
$72,560 - $115,440 a year
Posted
Job description

Primary Location US-IL-Northfield

JOB SUMMARY:

Under general supervision, the Regulatory Specialist is responsible for planning and executing operational regulatory activities necessary to store and distribute regulated products. Prepare comprehensive regulatory strategies for regulated product distribution ensure the content, context, organizations and quality of supporting information is sufficient to meet all regulatory requirements, commitments, and agreements. May review complex regulatory issues with RA management and other team members by applying their specialized experience to solve issues and complete short-term department goals.

MAJOR RESPONSIBILITIES:

  • In support of business priorities, determine the requirements for completing and maintaining product submissions and regulatory filings for storage and distribution.
  • Communicate requirements of regulations to internal or external customers. Recommend regulatory pathways and strategies.
  • Review and provide feedback on documentation and supporting evidence to ensure applicable regulatory requirements are met.
  • Complete and maintain regulatory filings by collaborating with internal and external groups, evaluating supporting technical in-formation, writing appropriate summary documentation, and supporting the response to non-conformances and questions from regulators.
  • Present project objectives with team members, solve problems, and act as a regulatory resource and subject matter expert.

Education

  • B.A. or B.S. degree in life science field (biology, microbiology, chemistry, etc.), engineering, medical technology, regulatory science, or related.

Work Experience

  • 2 years of experience in distribution of regulated products, regulatory affairs or quality assurance.

Knowledge / Skills / Abilities

  • Understanding of the current Regulatory environment and demonstrating the ability to perform within.
  • Applied knowledge of FDA regulations and guidelines or state licensing and distribution requirements.
  • Ability to evaluate information to determine compliance with standards, laws, and regulations.

Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization. The anticipated salary range for this position is $72,560-115,440. This salary range is an estimate and the actual salary will vary based on applicant’s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold. Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For a more comprehensive list of our benefits please click here. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.

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