Candidate should be interested in learning about a pharmaceutical manufacturer’s processes and practices to meet state and Drug Enforcement Administration regulatory requirements for the handling, storage, processing, and reporting of controlled substances. The candidate will learn the life cycle of controlled drug product from procurement of active pharmaceutical ingredient to sale/destruction of finished product within the DEA closed loop system. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.
This is a role working Monday through Friday from 8:00 AM - 4:00 PM EST based on site in our Bloomsbury, NJ location.
What The DEA Compliance Intern Does Each Day
Manage and coordinate all DEA related activities at multiple production facilities
Conduct year end and biennial inventory and report ARCOS quarterly reporting and cycle count inventory via DEA website
Responsible for implementing and gathering data to support YERS inventories
Coordinate all movement of control substances from manufacturing through analytical testing
Train internal individuals on controlled substance Standard Operating Procedures
Maintain compliance of all DEA, State and Board of Pharmacy registrations
Coordinate all controlled substance destruction with appropriate Quality and Logistics departments
Responsible for all necessary DEA registration and ordering forms (DEA 222)
Responsible for regulatory requirements for CSOS setup and maintenance
Responsible for submitting CII quotas to DEA, maintain organized DEA files on related activities
Coordinate and document DEA audits for sites and issue audit reports to management upon completion
Remain current on DEA regulations to address organization business needs
Our Most Successful DEA Compliance Intern
Are detail-oriented with strong verbal and written communications skills
Motivates others, shares knowledge, builds high performing team, shows respect towards others, gives constructive feedback
Display eagerness to learn and continuously improve, adapt quickly to change, and apply sound judgment
Foster team environment, invest in team members and peers by inclusion and listening, recognize employees effectively, demonstrate trust
Minimum Requirements For This Role
Legally authorized to work in the job posting country
High school diploma or GED from recognized institution or organization required
Must be actively pursuing a bachelor's degree from an accredited institution, with an anticipated graduation date within the next two years
Must be in good standing with accredited institution where pursuing degree
Microsoft Word and Excel skills
Benefits Of Working At QuVa
Set, full-time, consistent work schedule
National, industry-leading high growth company with future career advancement opportunities
About QuVa
QuVa is a national, industry-leading provider of pharmacy services, including ready-to-administer sterile outsourcing and advanced AI-generated insights providing clarity for revenue capture and inventory management. QuVa Pharma delivers essential medications in injectable formats critical for effective patient care. LogicStream, a QuVa company, partners with health systems to aggregate, normalize, and analyze large amounts of complex data through AI and machine learning tools that generate actionable insights supporting revenue optimization, inventory management, and inventory-related workflows. Through QuVa’s integrated solutions, health systems can transform pharmacy management to achieve greater value by operating more efficiently and effectively as they deliver high-quality patient care.
QuVa is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. QuVa's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with QuVa is “at will.”
Seniority level
Internship
Employment type
Full-time
Job function
Education and Training
Industries
Pharmaceutical Manufacturing
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