Job Summary
This position requires an individual who has the experience and ability to educate offices about Epicur products or services in order to increase business growth.
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
Supports cGMP analytical chemistry analysis associated with processes related to routine testing, stability testing and method transfer.
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 the Manufacturing Manager.
Job Summary
This position performs a wide range of administrative responsibilities and clerical support activities related to office management, general administration, sales and marketing, and special projects as needed. The individual must be professional, have a strong work ethic, be highly organized and have the ability to work autonomously as well as in a team.
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
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 in collaboration with other Supply Chain Technicians and the Production/Procurement Coordinator under the direct supervision of the Manufacturing Manager.
Job Summary
The Validation Specialist is responsible for commissioning, qualifying, and validation activities associated with equipment and processes related to cGMP operations.
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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