The base salary for this position ranges from $110,000 - $140,000 per year. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, with this position within the first 12 months.
Responsibilities
Achieve all product sales performance goals and objectives for geographical assignment (territory).
Distribute samples and record sample transactions in accordance with Company Policy and PDMA guidelines.
Develop comprehensive and accurate sales presentations using all approved marketing and selling materials.
Maintain proficient knowledge of promoted product disease states and indications.
Deliver proficient sales presentations to a defined list of current and prospective customers with a frequency based on assigned call goals.
Requirements
Bachelor's Degree (BA/BS) Business, Life Sciences, Marketing or relevant field
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. Salary Range 107,545.40USD -145,502.60 USD
Responsibilities
Own, manage, and close quality records (Supplier Event Notifications and Investigations (EN/SICAR), Change Controls, Deviations, Corrective and Preventive Actions (CAPAs), and CAPA-Effectiveness Verifications) under the company's quality management system procedures and ensure compliance with regulatory agency requirements.
Facilitation of cross-functional teams (internal and external to the site) with the goal of achieving robust and detailed investigation performance or timely implementation of supplier/raw material related changes.
Partner cross-functionally across the network to ensure maturity and execution of robust quality record process.
Lead investigation teams to identify meaningful root causes and robust corrective and preventative actions by effectively utilizing advanced root cause analysis tools (Causal Factor Analysis, Fault Tree Analysis, Kepner-Tregoe, etc.).
Manages closure of multiple quality records simultaneously and in a timely matter (Deviations, Change Controls, ENs, SICARs, CAPA, CAPA-EV).
Lead the operational implementation of the Pharmacovigilance Quality Management System within the Global Patient Safety functional area.
Locations (3)
Gent, Belgium
Switzerland
United States
Responsibilities
Provide pharmacovigilance oversight for the management and operational maintenance of third‑party contractual obligations.
Drive the growth of the GPS Quality Management function.
Drive & implement the Comprehensive Training Program.
Manage GPS Procedural Document activities.
Actively participate in and coordinate GPS Audit & Inspection Readiness, Support & Management.
Requirements
Bachelor’s degree in pharmacy, nursing, healthcare or other life‑science or technical field or country equivalent combination of education and experience