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Validations Specialist

2 months ago

Pensacola, United States Skywalk Group Full time
Are you a detail-oriented professional with a passion for upholding the highest standards of quality and compliance?

Pegasus Laboratories, Inc., an innovative veterinary pharmaceutical and medical product company, is hiring a Validation Specialist to join its team in Pensacola, FL.

As a Validation Specialist, you will create and update Product Validation Master Plans (PVMP) and Validation Summary Reports (VSR) for annual FDA reporting. Responsibilities include performing cleaning, process, and packaging validations, as well as managing the Product Cleaning Validation lifecycle post-FDA approval through ongoing cleaning verification.

Position Responsibilities:
•Independently conducts sampling and sample preparation to support cleaning, process, and packaging validation protocols
•Develops operational and cleaning procedures to support manufacturing equipment and product lines
•Oversees ongoing product validation activities to ensure the completion of cleaning validations
•Monitors equipment and facility commissioning projects through protocol development and execution
•Supports operations in facility environmental monitoring and the calibration program

Benefits & Perks:
•Competitive compensation
•Healthcare coverage
•Flex Spending Account
•401(k) retirement plan
•Disability Insurance
•Pet Insurance
•Employee Stock Ownership Plan (ESOP)
o What is ESOP? It's an ownership stake in the company that provides an additional form of compensation directly tied to PBI-Gordon's financial success. All regular employees are eligible to participate in the ESOP and will be partially vested after two years with the companies; all employees are 100% vested after six years of service

Position Requirements:
•AA degree, professional accreditation, or coursework in a relevant field or equivalent experience required; Bachelor's or Master's degree in a related discipline preferred
•3+ years experience of FDA regulated manufacturing, facilities, quality, or laboratory environment with an AA degree OR 1+ years of experience with Bachelor's or Master's degree
•Pharmaceutical, cGMP, and/or experience with an FDA-regulated facility required
•Familiarity with SUPAC, USP, ICH, and VICH guidelines and strong technical writing/documentation skills

Take the next step toward an exciting career and help contribute to our mission of delivering exceptional quality and innovation-apply today

This organization is an Equal Employment Opportunity employer and a supporter of affirmative action with a strong commitment to diversity, equity, and inclusion. All qualified applicants are considered for employment without regard to membership in any protected class by federal, state, and/or local laws.