Hobson Prior is seeking a PV Quality Management Associate to join our client's team in New Jersey. In this role, you will support the management of quality activities related to drug safety and compliance. You will assist with monitoring performance, managing documents, preparing for audits, and coordinating training programs. This position requires strong organizational skills and attention to detail.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
- Help monitor and document key performance indicators and compliance metrics.
- Assist in managing quality issues and implementing corrective actions.
- Support preparation and coordination for audits and inspections.
- Collaborate on training programs and maintain training records.
- Manage procedural documents and ensure they are up-to-date.
Key Skills and Requirements:
- A bachelor's degree is required.
- Experience in drug safety or related fields.
- Familiarity with FDA, EU regulations, and international guidelines is preferred.
- Understanding of clinical and pharmacovigilance procedures is beneficial.
For more information, please contact William Tyler.
Apply now
If you are interested in learning more or applying to this exciting opportunity then please click 'Apply' and upload a copy of your CV. Alternatively for further details or to talk directly to a life sciences recruitment specialist directly please select 'Contact me' at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
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