Regulatory Compliance Officer

Sanmina-SCI

$80K — $100K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a scientific discipline
  • 5+ years in a Quality/Regulatory and manufacturing environment
  • Expert knowledge of FDA regulations
  • Strong written and verbal communication skills
  • Proficient in MS Office and Internet resources
  • Professional demeanor across diverse settings
  • Willing and able to travel globally
  • Experience with Device submissions (510K, PMA, IDE) is a plus.

Responsibilities

  • Develop and implement strategies for the medical division
  • Coordinate compliance with quality and regulatory initiatives
  • Act as a liaison with the FDA and other regulatory agencies
  • Review technical reports for regulatory adherence
  • Recommend policies for FDA compliance
  • Assist in scheduling and tracking project activities
  • Stay updated on laws and regulations affecting product development
  • Prepare and review Standard Operating Procedures (SOPs).

Benefits

  • Work for a recognized technology leader in EMS
  • Opportunity to contribute to critical healthcare products
  • Engage with regulatory agencies on a professional level
  • Global travel opportunities
  • Collaborative work environment with a focus on quality and compliance.
Full Job Description
Regulatory Compliance Officer

Job Purpose:

Sanmina, Carrollton, Texas is looking for a Regulatory Compliance Officer to coordinate and prepare documentation packages for regulatory submissions, internal audits and inspections from all areas of the company.

Nature of Duties:
  • Develop and implement strategies to facilitate the progress of Sanmina's worldwide medical

division.
  • Work with assigned Medical Division facilities on conformance to company quality and

regulatory initiatives.
  • Serve as liaison with the FDA and other regulatory agencies as assigned; Interface with

plant management teams, customers and notified bodies as assigned;
  • Review technical reports and summary documents for adherence to regulatory guidelines,

strategies, and commitments.
  • Recommend regulatory policies to assure adherence to FDA requirements.
  • Contribute to the modification, development and implementation of company

practices and policies for quality and regulatory affairs.
  • Assist in the scheduling and tracking of project and operational activities for the

Medical Division.
  • Keep abreast of all pertinent laws, regulations and guidance and provide insight on

current regulations and guidance documents relevant to product development

projects.
  • Provide input on regional regulatory strategies and implementation activities.
  • Prepare Standard Operating Procedures and provide review of SOPs as necessary.


Education and Experience :
  • Bachelor's degree in a scientific discipline
  • A minimum of 5 years experience in a Quality/Regulatory and manufacturing environment.
  • Expert knowledge of FDA regulations
  • Strong written and verbal communication skills necessary
  • Proficient use of technology including MS Office and Internet resources
  • Must demonstrate professionalism in all working environments.
  • Must be able/willing to travel globally.
  • Experience with Device submission is a plus. (510K, PMA, IDE)

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