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 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 the Manufacturing Manager.
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
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
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
The LIMS Specialist works directly with the Director of Quality and Leads to the development and support of the LIMS system at Epicur Pharma.
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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