Regulatory Affairs Associate Job at Medline Industries, Santa Clarita, CA

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  • Medline Industries
  • Santa Clarita, CA

Job Description

Value Proposition As a leading partner in healthcare, Medline Canada's sole purpose is Together Improving Care – this means being deeply committed to the health and well-being of our customers, employees, partners and our communities. We employ a diverse group of top talent focused on growing and making a difference in the lives of Canadians, coast-to-coast. Compensation is only one part of the Employee Value Proposition that Medline Canada offers our employees. As part of our mission, we offer one of the most competitive and engaging employee experience programs in Canada, which includes: Collaborative work environment with highly engaged employees Market competitive compensation and benefits plan, including LTD & Insurance DPSP match program Annual Employee Appreciation Week Paid vacation and personal days Lifeworks® Employee Assistance Program (EAP) Resources supporting mental, physical, family and financial well-being Career growth and training programs Open communication with Senior Leaders Tailored incentives for eligible employee groups, such as home office reimbursement and Sylvan Learning Centre credit Employee referral program Education support programs Fitness subsidy Recognition programs Social activities And much more…

JOB SUMMARY

The Regulatory Affairs Associate assists with the preparation of regulatory applications and helps overall in obtaining regulatory clearance for selling products on the Canadian market. This is an entry-level role, supporting the RA department

CORE JOB RESPONSIBILITIES

  • Perform regulatory screening of new products to ensure compliance with Health Canada requirements.
  • Prepare summary reports for devices, drugs and NHPs, but collecting and compiling data, as well as providing an analysis.
  • Assist in the preparation and submission of medical device licence applications, and support amendments and renewals of MDELS and DELs.
  • Manage and requisition regulatory and quality documents, maintaining accuracy and timely access for stakeholders.
  • Respond to customer requests for regulatory information.
  • Respond to miscellaneous requests from Medline personnel on regulatory matters and other miscellaneous duties as required from time to time.
  • Work directly with Medline Corporate Divisions to obtain required information for product applications. Medline Industries

Job Tags

Home office,

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