Clinical Quality Specialist: CAPA, Audits & Compliance

ProPharma; Greater London; On-site; GBP 30,000 - 45,000; Full time

Job summary

ProPharma seeks a Quality Specialist in Greater London to ensure compliance with quality standards in Clinical services. The role includes generating reports, analyzing quality deviations, and supporting audits. Candidates should have a university degree and at least 2 years in a Quality Assurance role, alongside knowledge of GxP systems. ProPharma offers an inclusive work environment, emphasizing continuous monitoring to enhance compliance and quality within the organization.

Qualifications

• Maintain compliance with GVP, GCP, and GDP requirements.
• Ability to identify trends and outliers.
• Requires proactive work with minimal supervision.

Responsibilities

• Generate and prepare reports on quality activities.
• Review, approve and communicate corrective actions.
• Track documentation related to quality metrics.
• Support external audits and regulatory inspections.
• Facilitate eQMS activities including document management.

Skills

Knowledge of Good Pharmacovigilance Practices

Excellent computer skills (Microsoft Word, Excel)

Analytical skills

Written and verbal communication skills

Attention to detail

Ability to organize and prioritize

Education

University degree and/or relevant work experience

Job description

ProPharma seeks a Quality Specialist in Greater London to ensure compliance with quality standards in Clinical services. The role includes generating reports, analyzing quality deviations, and supporting audits. Candidates should have a university degree and at least 2 years in a Quality Assurance role, alongside knowledge of GxP systems. ProPharma offers an inclusive work environment, emphasizing continuous monitoring to enhance compliance and quality within the organization.