Hiring.Camp

Senior Auditor, Quality Assurance

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·

2 weeks ago

Location
Mexico, Mexico City
Workplace
Onsite
Type
Full-time
Department
IT
Seniority
Senior
Experience
5+ years
Visa
Not sponsored
Closing date
Today
Source
Workday

Description

Senior Auditor, Quality Assurance

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


We are currently seeking a Senior Auditor, Quality Assurance to join our diverse and dynamic team. As a Senior Auditor, Quality Assurance at ICON, you will play a pivotal role in ensuring the quality and compliance of clinical trials, interpreting regulatory requirements, and contributing to the advancement of innovative treatments and therapies.


What you will be doing

  • Leading and conducting comprehensive audits of clinical trial processes, systems, and documentation to ensure compliance with regulatory standards and guidelines.

  • Contributing to inspection readiness and participating in health authority inspections as needed.

  • Developing and implementing audit plans and strategies to assess the effectiveness of quality management systems.

  • Providing expert guidance and practical recommendations to stakeholders regarding GCP and quality assurance best practices.

  • Identifying areas for improvement and contributing to the continuous enhancement of QA programs and initiatives.


Your profile

  • Bachelor’s degree in Life Sciences, Pharmacy, or a related field, or equivalent relevant experience.

  • Minimum of 5 years of experience in quality assurance, auditing, or inspections within the pharmaceutical, biotechnology, or CRO industry.

  • Proven experience with GCP’s (Good Clinical Practices), site audits, and clinical quality oversight. (NOT other GxP’s)

  • Strong understanding of regulatory requirements and quality systems related to clinical research.

  • Analytical mindset with excellent problem-solving abilities and attention to detail.

  • Effective communication and interpersonal skills, with the ability to work collaboratively across cross-functional teams.

  • Advanced English proficiency — fluent in reading, writing, and speaking.

#LI-DT2

#LI-Remote


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

Skills

GCPClinical TrialsCompliance

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