Manager CPVQA - 1 Year FTC (Remote UK & Ireland)
1 Days Old
In addition, the Manager will support Global Quality/ R&D leaders in providing strategic input and tactical implementation for pharmacovigilance system activities and projects, identify and communicate compliance risks, oversee action plans to mitigate risks (if applicable), and be actively involved in inspections and inspection-readiness activities. This person will participate in interdepartmental teams meetings and at times may be asked to perform activities to support other GxP areas, quality operations, and global quality systems.
Gain and maintain professional expertise and knowledge of local and international regulations relative to pharmacovigilance system and quality
Contribute to the execution of Global PV system audit strategy, and implementation within the Quality Management System
participate in the development of SOPs for Quality or PV System stakeholders
Support updates of the quality related sections in the Pharmacovigilance System Master File (PSMF) or similar documents
Perform execute and evaluate PV-System auditee risk assessments
Coordinate and implement strategic audit plans for pharmacovigilance system activities that include service providers, vendors, business partner, and internal audits.
Present QA findings/observations to in-house staff and, if appropriate, to the responsible service provider, vendor, or partner company.
Contribute to the evaluation of corrective and preventative action (CAPA) findings to identify quality-related signals and trends for improvement; Participate in inspection readiness and inspections as assigned. May perform one or more inspection roles during an inspection (e.g. inspection readiness training, runner, scribe, backroom lead, SME preparation, QA checks, etc.)
Identify and escalate critical quality issues to senior Quality management
Contribute to the development of continuous quality process improvements and the identification of identifying root causes for investigations and effectiveness checks if appropriate
Represent CPVQA within interdepartmental teams / project groups and innovation projects
Maintain current training in accordance with the training curriculum
This position may require up to 30% travel
Established Pharmacovigilance or Quality professional Strong GVP knowledge & expertise
Disciplined, detail orientated, and strong time management skills
Inspection experience with FDA, MHRA (or other EU Competent Authorities); experience with emerging markets Regulatory Authority such as PMDA a plus.
Bachelor’s degree in a related field is required; Master’s degree in management, leadership or scientific discipline a plus.
Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.
The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation.
- Location:
- London
- Job Type:
- FullTime