QA GCP Auditor

Our European activities are growing rapidly, and we are currently seeking a full-time QA GCP Auditor to join our Quality Assurance team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous GCP expertise and can develop and grow within an individual career path, then this is the opportunity for you.

We are interested in office-based individuals in Prague. Hybrid working is available following 6 months of employment. To support the commute into the office, Medpace offers a generous commuting allowance benefit.

Please note that we are looking for individuals who are available to travel across Europe as necessary and up to 70% of your working time.

Candidates must have direct GCP QA experience to be considered.

• Work as a trusted partner with Medpace operations to promote a culture of continuous improvement;
• Coordinate and conduct internal system audits and external investigative site/vendor audits;
• Create, maintain, and revise departmental Standard Operating Procedures, forms, and templates;
• Develop training materials and applicable tests and guides;
• Work with outside clients/sponsors.
• Host Sponsor audits and Regulatory Inspections
• Act as QA Project Leader, managing timelines and coordinating workload amongst QA Auditors

• Bachelor’s degree in life sciences or nursing;
• 2 or more years of experience in a QA GCP department in a related industry;
• Experience of GCP site audits and vendor audits is highly preferred
• Excellent written and verbal communication skills
• Exceptional teamwork skills
• Ability to work independently.

Travel: Average of 50% across Europe

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

• • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
  • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

• • Office based environment with on-site mentors
  • Defined career paths with clear advancement opportunities
  • Industry renowned onboarding and training programs designed to accelerate professional development
  • Ongoing training and continuous learning opportunities throughout your career
  • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

• • Competitive compensation programs that recognize and reward performance
  • Comprehensive health, wellness, retirement, and PTO benefits
  • Office based culture with occasional WFH that provides flexibility for eligible positions after training
  • Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.