For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
The Quality Manager provides leadership for quality activities and drives positive change and process improvement in the assigned region. This role functions as an independent and objective entity and operates in a multifaceted function by working and supporting various operational teams. The Quality Manager performs quality activities as outlined in ProPharma Group’s Quality Policy and procedures. Serves as the central/regional point of control for Audit Management, Deviation and CAPA Management, Document Control, and other Quality Management System activities. Develops, manages, and executes quality management processes to ensure quality standards are maintained and compliant with regulatory requirements.
Essential Functions Include:
Personnel Management
General
Qualifications:
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.