Global Medical Device QA & Regulatory Consultant

UL Solutions

Mexico

On-site

MXN 350,000 - 700,000

Full time

2 days ago
Be an early applicant

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

UL Solutions in Mexico seeks a Regulatory and Quality Affairs Consultant to support global medical device registrations, liaise with authorities, and guide clients through regulatory pathways.

You will prepare submissions, analyze requirements, brief teams, and help ensure compliance across markets, using strong English communication and MS Office skills. Collaboration with local partners and senior consultants is common.

Qualifications

  • Bachelor's degree in Medical, Engineering or Science field preferred.
  • Strong written and verbal English communication skills.
  • 2–5 years of Quality Assurance and/or Regulatory Affairs experience in medical devices (regulatory, submissions or quality support).
  • Consulting experience a plus.
  • Excellent attention to detail and ability to perform regulatory research.

Responsibilities

  • Assist with preparation and submission of medical device registrations to regulatory markets.
  • Prepare renewals or amendments and support project teams.
  • Develop knowledge of submission requirements and communicate processes clearly to clients.
  • Assist with client documentation review and gap analysis; advise on data acceptability.
  • Escalate complex issues to senior experts and support resolution.
  • Prepare regulatory reports and lead multi-market research projects as needed.
  • Interact with local regulatory authorities on behalf of clients where appropriate.

Skills

English proficiency
Regulatory affairs
Medical device knowledge
Consulting experience
Attention to detail

Education

Bachelor's degree in Medical, Engineering or Science

Tools

Microsoft Office

Job description

UL Solutions in Mexico seeks a Regulatory and Quality Affairs Consultant to support global medical device registrations, liaise with authorities, and guide clients through regulatory pathways.

You will prepare submissions, analyze requirements, brief teams, and help ensure compliance across markets, using strong English communication and MS Office skills. Collaboration with local partners and senior consultants is common.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Global Medical Device Regulatory & QA Consultant
Global Medical Device Regulatory & QA Consultant

UL, LLC • Mexico

Remote
MXN 450,000 - 700,000
Quality & Regulatory Affairs Consultant
Quality & Regulatory Affairs Consultant

UL Solutions • Mexico

On-site
MXN 350,000 - 700,000
Regulatory Affairs Analyst — Global Medical Devices
Regulatory Affairs Analyst — Global Medical Devices

Edwards Lifesciences Gruppe • Ciudad de México

On-site
MXN 420,000 - 800,000
Quality Assurance Engineer - Medical Devices, GMP & QMS
Quality Assurance Engineer - Medical Devices, GMP & QMS

Oferta confidencial • Tijuana

On-site
MXN 180,000 - 240,000
Global QA & Regulatory Director - Life Sciences Logistics
Global QA & Regulatory Director - Life Sciences Logistics

DHL Supply Chain • Cuautitlán Izcalli

On-site
Confidential
Consultant, Regulatory Affairs and Quality
Consultant, Regulatory Affairs and Quality

Parexel • Ciudad de México

On-site
MXN 900,000 - 1,150,000
Regulatory Affairs Specialist - Mexico (Hybrid)
Regulatory Affairs Specialist - Mexico (Hybrid)

Parexel • Ciudad de México

Hybrid
MXN 900,000 - 1,150,000
Senior QA Design Transfer & Validation Engineer
Senior QA Design Transfer & Validation Engineer

Merit Medical • Tijuana

On-site
MXN 900,000 - 1,300,000
Global Quality Leader – Medical Devices & Compliance
Global Quality Leader – Medical Devices & Compliance

WS Audiology • Tijuana

On-site
MXN 900,000 - 1,300,000
Global Quality Systems & Compliance Specialist
Global Quality Systems & Compliance Specialist

Signant Health • Ciudad de México

On-site
MXN 350,000 - 700,000