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Regulatory Affairs Specialist III

Phoenix, AZ, United StatesPosted 113 months ago
ContracthybridAssociate

Job Description

JOB DESCRIPTION:

The Regulatory Affairs Specialist III works with a team of regulatory affairs professionals to ensure the establishment of best practices within the assigned area of responsibility.

Key responsibilities/essential functions:

  • Support continuous improvement activities, including such areas as regulatory procedure development and documentation, standards compliance, and metrics development and implementation.
  • Support regulatory compliance and optimization of quality system procedures relating to new product registration submissions and post market reporting through the development, maintenance and improvement of documented processes.
  • Support regulatory inspections as required
  • Work closely with regulatory, engineering, marketing, legal, and other professionals across the company to communicate company-wide programs and processes for regulatory compliance.
  • Work with regulatory colleagues to ensure a consistent approach to regulations is adopted throughout the business within areas of responsibility.
  • Collect & summarize performance metrics to identify program weaknesses & recommend improvements in procedures or oversight.

REQUIRED QUALIFICATIONS:

  • Bachelor’s Degree (or international equivalent) in a related field such as: Regulatory Science, Biomedical Engineering, Biology, Chemistry, English (with a technical writing emphasis), Legal Studies, Law, Nursing, Physician Assistance, Pharmaceutical Science, Pharmacy OR minimum of 8 years progressive regulatory affairs experience in medical device or pharmaceutical industry or medical product regulation agencies, including knowledge and experience applying drug or device laws and regulations
  • 5 years of relevant work experience
  • Strong analytical skills
  • Ability to work in a team environment with minimal supervision on projects and activities
  • Ability to prioritize, plan & evaluate deliverables
  • Knowledge & experience conducting scientific, regulatory, legal, or business research.
  • Excellent verbal and written communication and presentation skills with the ability to communicate in English in an easy to understand manner
  • Experience using spreadsheet and presentation software

Thanks

Warm regards
Avleen Kaur
732-318-6945

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Regulatory Affairs Specialist III at Integrated Resources INC | Renata