Job Summary
This position performs a wide range of bookkeeping and administrative activities. The individual must be professional, have a strong work ethic, high-level of confidentiality, be highly organized and have the ability to work autonomously as well as in a team.
Job Summary
This position requires an individual who has the experience and ability to handle high call volume in an active call center environment. They must possess enthusiasm, diligence, and resilience.
Job Summary
The Lead Stability Coordinator is a role within a 503B Outsourcing Facility responsible for managing and developing stability studies in accordance with CFR, ICH, and applicable regulatory guidance. This includes protocol development, managing study execution, stability investigation, data management, and data interpretation. The Lead Stability Coordinator reports directly to the Director of Quality.
Job Summary
This position requires an individual who can work within a cGMP environment in collaboration with Operations/Manufacturing Managers and the Production/Procurement Coordinator. The successful candidate must be focused on achieving individual and team productivity goals while maintaining a high level of accuracy.
Job Summary
The Microbiology Analyst I is responsible for supporting microbiology procedures, assisting in investigations, and performing routine analysis of raw material and finished product according to established specifications and procedures.
Job Summary
The Quality Assurance Analyst is responsible for ensuring cGMP standards are maintained to ensure
process and product quality.
Job Summary
The Quality Assurance Manager is a leadership role within a 503B Outsourcing Facility responsible for ensuring FDA compliance is met in accordance with 21 CFR Part 11, 210, and 211. This includes managing quality systems, quality procedures relating to raw materials and finished product, product stability, managing day-to-day operations, and finished product release. The Quality Assurance Manager reports directly to the Director of Quality.
Job Summary
This position requires an individual who can work collaboratively with production personnel to optimize
quality aspects of operations.
Job Summary
Quality Control Analysts are responsible for ensuring the quality of materials and that finished drug products are manufactured to meet current Good Manufacturing Practice (cGMP) and Epicur Pharma standards.
If you are interested in applying to any of the positions listed above, please email your resume to recruiter@stokeshealthcare.com.
Thank you for your interest in becoming part of Epicur Pharma®, a division of our Stokes Healthcare team.
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