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!

The Analytical Chemist performs routine and non-routine analytical quality control analysis of raw materials, in-process, finished products and stability samples in compliance with GMPs and corporate standards.

• Perform testing of raw materials as described in compendia or by vendor supplied methodology
• Perform testing of in-process, finished and stability samples versus specifications
• Responsible for documenting all lab work per cGMP and company standards
• Management and ownership of laboratory systems such as laboratory purchasing systems, analytical standards, calibrations, etc.
• Working with instrumentation such as HPLC, GC, FTIR, UV-Vis, pH meter, and Karl Fischer
• Testing performed in a high quality and timely manner and meets all procedure and regulatory requirements
• Writes and revises specification documents with their associated test sheets and SOPs
• Must be able to understand the purpose and objective of validation protocols
• Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
• Incorporates the company’s core values of Integrity, Innovation, Partnership and Pride daily by aligning actions with department goals and company culture
• All other duties as may be assigned

Qualifications

• Education: BS in Chemistry or related science field.
• Experience: 1 years in Pharmaceutical industry or GMP laboratory.
• Specialized knowledge: USP Testing & Standards, GMP Requirements for Pharmaceutical Laboratories, ICH Guidelines & Eur.Pharm. Testing & Standards.
• Experience and knowledge of HPLC, GC, AAS and Wet Chemistry procedures, etc.
• Knowledge of Laboratory systems for Reference Standards, Chemical Inventory, Calibrations, Volumetric Solution Preparation and Expiration, Notebook documentation standard, calculations and reporting standards.
• Excel and Microsoft Word
• Other skills:
• Experience in cGMP documentation
• Knowledge of USP/NF/EP testing procedures
• Attention to detail
• Able to communicate and listen effectively
• Effective verbal and written communication skills
• Ability to follow written procedures and document all activities in an accurate manner
• Ability to work effectively in a team environment
• Ability to perform testing with high precision and accuracy