At a Glance
- Tasks: Manage quality deviations and support the Quality Management System across departments.
- Company: Join a leading global clinical trials organisation focused on quality and compliance.
- Benefits: Competitive salary, professional development, and opportunities for career advancement.
- Other info: Collaborative environment with a focus on training and cross-functional teamwork.
- Why this job: Make a real impact on quality standards in clinical operations and ensure compliance.
- Qualifications: Scientific degree, 3+ years in QA or clinical operations, and strong English skills.
The predicted salary is between 45000 - 55000 £ per year.
Worldwide Clinical Trials is seeking an experienced QA professional to manage deviations and support the Quality Management System across the department.
You will contribute to sustaining high QA standards and ensure compliant documentation and recordkeeping.
The role emphasizes training development and cross-functional collaboration.
Ideal candidates hold a scientific degree, 3+ years in clinical operations or QA, and strong English proficiency, with experience in CAPAs and audit support.
#J-18808-Ljbffr
Senior QMS Specialist - Quality & Compliance Leader employer: Worldwide Clinical Trials
Worldwide Clinical Trials is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals passionate about clinical research. With a strong emphasis on employee growth, the company offers numerous opportunities for skill development and career advancement, all while working in a diverse environment that values creativity and teamwork. Located in a vibrant area, employees benefit from a supportive atmosphere that encourages meaningful contributions to patient engagement activities.
