Pegasus Laboratories, Inc.

Pegasus Laboratories, Inc. is a full-service Contract Development and Manufacturing Organization, or CDMO, with a very special purpose: improving the lives of animals. Through our leading veterinary brand, PRN Pharmacal, we create trusted veterinary products that promote animal wellness, including behavior modification, urinary incontinence, and seizure management. Our team of professionals, including manufacturing, quality assurance, business development, scientists and chemists, regulatory experts, and veterinarians, offers the complete package, from idea through development and regulatory approval, to production and marketing.

Pegasus Labs, part of the PBI-Gordon Companies, Inc., is 100% employee-owned with more than 500 employee-owners, working together in pursuit of mutual success. We are growing – come join us!

Job Summary:

The Packager Line Lead I will be responsible for reviewing all batch records for completeness to ensure the batch records accurately reflect the process times, equipment, and personnel involved in the packaging of a product lot. General labor duties as assigned. Monitor and ensure cGMPs and our SOPs are followed. All other duties assigned by management.

• Work with the training department to ensure all current and new personnel are trained and current and all documentation of training is complete and up to date.
• Ensure personnel follow cGMPs and SOPs during the process and ensure the suite is in a state of compliance.
• Responsible for ensuring equipment and rooms are documented in correct logbooks.
• Coordinate with the maintenance department with any equipment repairs needed.
• Review the completed Batch Records for completeness and correctness.
• Responsible for evaluating personnel and providing feedback to supervisor and personnel during semi-annual and annual reviews
• Provide training on all equipment assigned to the production department.
• Any additional duties that may be assigned by management.

Qualifications:

• Education: High School Diploma required.
• Experience: 2 years’ experience in a FDA/cGMP regulated production facility, with at least 1 year in a leadership role preferred or an associate’s or bachelor’s degree in lieu of leadership experience.
• Specialized knowledge or training: Production equipment setup and operation.