Search Jobs
Quality Management Associate, PV Quality Management, CSPV
211 Mount Airy Rd Basking Ridge, NJ 07920 US
Job Description
Target Pay Rate: 25-27.86hr **salary will be commensurate with experience
Job Description:
This position supports the head of PV Quality Management in the delivery and oversight of global and regional PV quality management activities including Compliance and performance monitoring, Quality management, Procedural document and records management, Audit/Inspection Readiness, and Training program management in alignment with Global PV strategy. This position is responsible for administrative support including but not limited to mailbox management, scheduling meetings, documentation of meeting minutes, organizing files and records, and other administrative tasks. This position is responsible for facilitation and/or coordination of activities including but not limited to following:
Responsibilities:
· Compliance and Performance Monitoring:
Coordinates activities for the monitoring of key performance indicators (KPIs) and compliance metrics of relevant PV activities including the compilation, collation, and documentation of data including non-compliant (late) single cases and aggregate safety reporting, adherence to PV agreements, signal management activities, and other relevant global KPIs and metrics.
· Quality:
Supports activities related to issue and CAPA management for all PV processes to ensure internal processes are evaluated, summarized, and fed back for implementation of actions and process improvement.
Track implementation of corrective and preventive actions related to findings from compliance monitoring, quality issue management, audits and inspections.
· Inspection and Audit Readiness:
Supports audit/inspection readiness activities including identification of PV subject matter experts (SME) and points of contact, notification of involved PV functions, and maintenance of PV SME contact lists.
Supports the collaboration with the Global R&D/PV-QA Audit and Compliance department in preparing for internal audits and regulatory inspections, including collection, review, tracking and provision of relevant documents and other inspection/audit requests.
Facilitates and coordinates relevant activities during all phases of audits/inspections (pre-, conduct, and post-)
· Training Program Management:
Collaborates with relevant CSPV functions to support onboarding and ongoing training activities.
Works with ALTOS Administrator to assign training, generate and access necessary training reports, and ensure proper training documentation.
Supports the maintenance of the training documents and materials including role-based curriculum. May participate in creating, reviewing, and revising training documents.
· Procedural Document Management:
Support activities related to documentation control, including retirement schedules, file structures, and delivery mechanisms (ALTOS, etc.).
Supports the lifecycle management of CSPV-related policies, procedures, and operating guidelines, including but not limited to SOPs, SOIs, guidance documents, associated forms, and templates). Supports process redesign initiatives by updating relevant documentation for changes to processes.
Supports the maintenance of all documentation files, including forms and templates, and communicates updates/revisions to documents.
Skills:
· 3 or more years of Pharmacovigilance experience in a pharmaceutical, biotechnology or related environment preferred
· Possesses knowledge of Food and Drug Administration (FDA) regulations, European Union (EU) regulations, and International Conference on Harmonization (ICH) guidelines preferred
· Possesses knowledge of Good Clinical Procedures (GCP) and Good Pharmacovigilance Procedures (GVP)
Education:
· Bachelor’s degree required, preferably in healthcare or life sciences field
Equal Opportunity Employer: We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert: Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.
Share This Job:
Related Jobs:
About Basking Ridge, NJ
Are you sure you want to apply for this job?
Please take a moment to verify your personal information and resume are up-to-date before you apply.