Quality Assurance Auditor II

KCR Placement is a full-service functional sourcing and recruitment provider. We specialize in high-speed and high-quality talent sourcing for the CRO, Pharmaceutical, Biotech and Medical Device industries across Europe. 
Our employees are KCR Placement's most crucial asset. We commit to placing our candidates at the center of all we do and prepare them for long-term career development and success with competitive benefits and vibrant work environment. 
The KCR Placement team is supported by a specialized referral network of expert professionals and is dedicated to providing sourcing services and client support from job requisition to job offer. 

On behalf of our partner, one of the global leaders in clinical research, we are seeking an experienced Quality Assurance Auditor to join their innovative and collaborative team.

In this role, you will be instrumental in upholding the highest standards of quality and compliance for clinical trials, applying regulatory expertise, and supporting the development of groundbreaking therapies and treatments.

Quality Assurance Auditor II

Location: Bulgaria or Poland (hybrid/ home-based)

Duties and Responsibilities:

• Assisting in the development and implementation of quality assurance strategies and processes to support clinical trial activities;

• Conducting comprehensive quality assessments and audits to ensure compliance with regulatory standards and guidelines;

• Collaborating with cross-functional teams to identify and address quality issues and implement corrective actions as needed;

• Participating in the review and approval of clinical trial documentation and data to ensure accuracy and completeness;

• Contributing to the continuous improvement of quality assurance practices and procedures.

Qualifications, Skills & Experience:

• Bachelor's degree in Life Sciences, Pharmacy, or related field; advanced degree preferred.

• Minimum of 2 years of experience in quality assurance within the pharmaceutical, biotechnology, or CRO industry;

• Familiarity with regulatory requirements and guidelines governing clinical trials (e.g., ICH-GCP, FDA regulations);

• Strong attention to detail and analytical skills, with the ability to identify and resolve quality issues effectively;

• Excellent communication and interpersonal skills, with the ability to collaborate effectively with colleagues and stakeholders at all levels.

Benefits:

• Various annual leave entitlements;

• A range of health insurance offerings to suit you and your family’s needs;

• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead;

• Global Employee Assistance Programme;

• Life assurance;

• Country-specific flexible benefits, including options like gym membership discounts, childcare vouchers, and more.

Our Privacy Policy

As KCR became part of the ICON group, your personal data will be shared with ICON and processed in accordance with privacy notice: https://www.iconplc.com/privacy/job-applicants

If you want your candidacy to be considered also for future recruitments, please send us an additional consent: “I agree to the processing of my personal data for any future recruitments conducted by ICON”. Such consent may be placed in your CV or electronic correspondence addressed to us. You can withdraw your consent at any time. Withdrawal of consent does not affect the legality of the processing carried out prior to its withdrawal.

KCR is an equal opportunity employer. In line with our motto, ‘We see human behind every number,’ KCR is committed to fostering an inclusive culture and maintaining a diverse, safe, and respectful working environment with equitable treatment for all.

We are committed to non-discriminatory practices and provide an equal opportunity for all qualified employees and job applicants within all employment sectors. We believe that in developing a desirable culture of belonging in which diverse perspectives and voices are welcomed and heard, the full potential of employees can be achieved.