Jr. Quality Engineer with English (with Life Science or Biomedical Experience)

Meet your

Carolina March
  • English
  • Spanish

A leading biomedical company is looking for someone ready to proactively bring new ideas to the team, push boundaries, and constantly look for innovation. The company believes in shared success and diverse ways of thinking, here you’ll learn, grow, and advance in an innovative culture.

As a Jr. Quality Engineer, you’ll support the quality team in implementing the Quality Management System, ensuring it’s understood and applied across the company. You’ll collaborate closely with other teams to maintain and enhance overall quality standards.

If you’re ready to drive the next generation of medical device development, we’re eager to hear from you.


  • Full professional level of English
  • Spanish is a plus 

Main Responsibilities

  • Support the quality department to maintain the overall quality system
  • Execute and maintain various QMS processes and assist process owners
  • Create and maintain QMS documentation, like standard operating procedures
  • Collaborate with departments to investigate non-conformances and process failures
  • Analyze and improve processes, implementing corrective actions to prevent compliance issues
  • Ensure QMS procedures are followed, providing advice on quality-related aspects
  • Support maintenance and calibration of equipment in labs and other premises
  • Oversee product acceptance and inspection activities as per procedures and Control Plans
  • Establish inspection standards, plans, and test methods for product realization
  • Support risk management activities
  • Lead and coordinate the creation and maintenance of FMEAs
  • Support internal and supplier audits according to ISO 13485 requirements
  • Manage eQMS system activities, including supplier monitoring and incoming inspection
  • Monitor lab activities to ensure compliance with Control Plans

Core Skills/experience

  • Master's degree or equivalent in Engineering, Life Sciences, or a related discipline (preferred)
  • 2-3 years of experience in quality assurance within the medical device industry
  • Strong knowledge of ISO 13485, ISO 14971, MDR 2017/745, and FDA 21 CFR 820
  • Collaborative team player with a positive attitude
  • Detail-oriented with a high degree of accuracy
  • Innovative and practical problem solver
  • Self-motivated and proactive

What’s on offer

  • Permanent contract

  • Hybrid working model

  • Private Health Insurance

  • 23 vacation days per year + 24th and 31st of December
  • A collaborative environment with a great team where innovative ideas flourish

  • Meaningful and challenging projects that have a positive impact on the industry and society as a whole

  • Payflow & Flexflow

  • Training bonus for professional development

  • Relocation Package

Our recruitment process

Step 1: Interview with our Recruiter to get to know you better

Step 2: Technical Interview with the Hiring Manager

Step 3: Interview with Head of HR

Step 4: Coffee chat with CEO