Regulatory Affairs Specialist jobs in Lancaster, PA

ABOUT US

Founded in 1981, Penn Veterinary Supply was created out of the belief that there is a better way to supply veterinarians with products and services. This belief remains at the core of everything we do. We proudly remain a family owned and operated business, free of corporate ownership. This enables us to best meet the needs of our customers on an individual basis without the pressure of answering to shareholders. We strive to set a higher standard of servicing the veterinary profession by focusing on our Power in Partnership model:

• Penn Vet is a Family-Owned Business that values our PEOPLE and yours.
• Our team is dedicated to providing SOLUTIONS for the veterinarians and entire staff at independent, privately held veterinary hospitals.
• We aim to be a true business partner that strives to consistently exceed your SERVICE expectations.
• We select partners who advocate for the importance of the veterinarian's recommendation of PRODUCTS that provide quality, savings, and value.

Penn Vet was born in Lancaster County, Pennsylvania, and has since grown to open branches in Michigan, Florida, and North Carolina.

ABOUT THE POSITION

Penn Vet is seeking a Regulatory Associate to help us continue to expand and grow. The Regulatory Associate will ensure that the company complies with industry specifications, standards, regulations, and laws. They will review operational practices, create and enforce compliance plans, and perform regulatory risk management. 

 
One (1) full-time position is available in our corporate location, Lancaster, PA: Candidates must be able to work Monday thru Friday from 8:00 AM – 5:00 PM

RESPONSIBLITIES

• Develops procedures and ensures compliance with corporate policies and regulatory interests. 
• Completes weekly temperature sensor reports as required.
• Monitors critical environmental systems for sensor alerts and makes appropriate notifications.
• Responds to internal and external regulatory requests including DEA, doctor, and state licensing inspections and reports.
• Organizes and facilitates internal and external audits.
• Completes manufacturer form requests, adverse action reports, and product authentications as required.
• Completes SOP edits as needed and coordinates associate reviews annually.
• Maintains current knowledge of local, state, and federal pharmaceutical laws. 
• Participates in Safety Committee & OSHA Staff Trainings & Tasks.
• Completes other related duties as assigned, customary to department and role.

QUALIFICATIONS

• Degree in Business or Biology with relevant regulatory/ pharmaceutical experience preferred. 
• Computer literate, proficient in Microsoft Office. 
• Proficient in understanding SOP protocol. 
• Strong analytical skills, attention to detail, well organized 
• Able to organize one’s own activities and manage multiple priorities. Must meet deadlines. 
• Excellent verbal, written, presentation, and overall communication skills.