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Job Summary
This position requires an individual who can work within a cGMP environment in collaboration with other Aseptic Processing Technicians under the direct supervision of the Manufacturing Manager. The successful candidate must be focused on achieving individual and team productivity goals while maintaining a high level of precision and quality.
Job Summary
Supports cGMP analytical chemistry analysis associated with processes related to routine testing, stability testing and method transfer.
Job Summary
This position requires an individual who can work within a cGMP environment in collaboration with members of the warehouse and cross-functional teams under the direct supervision of the Manufacturing Manager.
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 other Manufacturing Technicians and under the direct supervision of the Aseptic Manufacturing Supervisor. The successful candidate must be focused on achieving individual and team productivity goals while maintaining a high level of precision and quality.
Job Summary
The Manufacturing Technician-Equipment Prep is responsible the set-up, cleaning and packaging of materials and equipment that will be used for batch production, while following appropriate procedures in a clean and safe work environment meeting all cGMP, FDA, DEA, OSHA and other applicable regulations. This individual will work with other Equipment Prep Manufacturing Technicians under the direct supervision of either the Manufacturing Manager or Aseptic Manufacturing Supervisor (dependent on area assigned (aseptic vs. non-sterile)).
Job Summary
This position requires an individual who can work within a cGMP environment in collaboration with other labeling technicians and under the direct supervision of the Manufacturing Manager. The successful candidate must be focused on achieving individual and team productivity goals while maintaining a high level of precision and quality.
Job Summary
This position requires an individual who can work within a cGMP environment in collaboration with other Manufacturing Technicians and under the direct supervision of the Manufacturing Manager. The successful candidate must be focused on achieving individual and team productivity goals while maintaining a high level of precision and quality.
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 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.
The scheduled work hours for this position are 12:00 pm to 8:30 pm.
Job Summary
The Procurement Manager (PM) is responsible for monitoring costs to assure competitive pricing from vendors. This individual will collaborate with suppliers and/or manufacturers to maximize inventory objectives and assist in optimizing cost of operation. This includes negotiation with suppliers to maintain and improve pricing terms, quality, and on-time deliveries as required for all materials, components, subcontracted finished goods, and equipment.
Job Summary
The Quality Assurance Analyst is responsible for ensuring cGMP standards are maintained to ensure
process and product quality.
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.
Job Summary
This position requires an individual who can work collaboratively with production personnel to optimize
quality aspects of operations.
Job Summary
This position requires an individual who can work within a cGMP environment and is hard-working, dedicated, and reliable. The successful candidate must be focused on achieving both individual and site goals by showing an innate ability to manage equipment, remediate both planned and unplanned issues, be flexible and respond effectively to changing priorities at a moment’s notice.
Job Summary
The primary responsibility of the Veterinary Equine Representative is to generate new business, continue to service and develop relationships and grow our business with existing customers, while providing the highest level of service and support. The position will encompass a large multi-state territory focusing sales coverage on Large Animal and Mixed Animal Practices with an emphasis on Equine.
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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All information provided on this site is for educational purposes only. Every effort has been made to provide accurate and up-to-date information. It is not intended to be used as medical advice for the diagnosis of health problems nor does it include all possible uses, actions, safety measures, side effects, or interactions. Please consult a healthcare provider or veterinarian for the diagnosis and treatment of any health conditions. Epicur Pharma® manufactured veterinary orders are for non food chain animals only. Epicur Pharma® is registered with the FDA as an outsourcing facility.
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