Eva Pharma
Pharmaceutical
QualityComplianceManager-EuropeCluster(Part-time)
Neural analysis suggests this role is
optimal for Manager candidates.
“Quality Compliance Manager - Europe Cluster (Part-time) at Eva Pharma. Skills: Quality Management System, GxP compliance, Regulatory inspections. Maintain Quality Management System. Improve Quality Management System”
What You'll Achieve.
Ensure organization remains inspection-ready; Ensure organization fully compliant with GxP
Industry & Context.
Process improvement
What They're Looking For.
Must Have
Degree in Pharmacy, Life Sciences, or related scientific discipline, 5-7 years of experience in pharmaceutical or healthcare quality management systems, Experience as a Responsible Person for Wholesale Distribution under German Medicines Act (AMG §52a), Knowledge of GxP requirements, Knowledge of German pharmaceutical regulations, Knowledge of EU compliance standards
What You'll Do.
Maintain Quality Management System
Improve Quality Management System
Manage quality documentation
Coordinate employee training
Coordinate qualification programs
Coordinate compliance records
Lead supplier qualification activities
Lead customer qualification activities
Lead service provider qualification activities
Conduct internal audits
Follow up on internal audits
Plan quality assessments
Conduct quality assessments
Follow up on quality assessments
Manage quality events
Manage process improvement initiatives
Oversee quality-related interfaces with manufacturers
Oversee quality-related interfaces with external service providers
Oversee quality-related interfaces with batch release partners
Prepare for regulatory authority inspections
Coordinate regulatory authority inspections
Support regulatory authority inspections
Ensure ongoing inspection readiness
How You'll Work.
Team & Collaboration
Interact with internal stakeholders; Interact with external stakeholders
Full Job Description
Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members. Job Summary The **Quality Compliance Manager (Part-Time)** is responsible for maintaining and continuously improving the German Quality Management System (QMS), ensuring compliance with German and EU pharmaceutical regulations. The role oversees quality processes, inspections, audits, training, supplier qualification, CAPA management, and quality oversight of external partners to ensure the organization remains inspection-ready and fully compliant with GxP requirements. ### Key Responsibilities * Maintain and continuously improve the local Quality Management System (QMS). * Manage quality documentation, including SOPs, forms, records, and periodic reviews. * Coordinate employee training, qualification programs, and compliance records. * Lead supplier, customer, and service provider qualification activities. * Plan, conduct, and follow up on internal audits and quality assessments. * Manage deviations, quality events, CAPAs, and process improvement initiatives. * Oversee quality-related interfaces with manufacturers, external service providers, and batch release partners. * Prepare for, coordinate, and support regulatory authority inspections while ensuring ongoing inspection readiness. ### Employment Type **Part-Time | Remote (Germany-based)** **Requirements** * Degree in Pharmacy, Life Sciences, or a related scientific discipline. * Minimum 5-7 years of experience in pharmaceutical or healthcare quality management systems. * Experience as a Responsible Person for Wholesale Distribution under German Medicines Act (AMG §52a). * Strong knowledge of GxP requirements, German pharmaceutical regulations, and EU compliance standards. * Manage multiple quality activities, and effectively interact
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