FAS Lab - Controlled Substance Compliance Associate
About Us
Since 1990, we've grown into a global leader in personalized medicine. Today, our +5,000 energetic employees are based in +80 locations across Europe, North America, South America, Africa, and Asia-Pacific, working together to support over 200,000 customers worldwide. From compounding and natural products to software, equipment, and genomics, we deliver smart, ready-to-use solutions that make healthcare better. We're passionate, science-driven, and always looking for new ways to improve lives.
About the Role
The Controlled Substance Compliance Associate will support the DEA compliance profile by acting as the primary entity responsible for all logistics associated with the daily activities for all Controlled Materials at Fagron Sterile Services. This dedicated position executes the logistics associated with raw material and finished product movements and required documentation, coordinates sample inspection and transfer, VI and labeling, inventory reconciliation, and correct disposal. The role ensures all CS-related activities occur consistently and serves as a liaison to other functional areas within FSS to foster a culture of awareness and DEA compliance.
Responsibilities
- Correct and consistent execution and documentation of all CS material transactions, including:
- Vault check-in/out
- Inventory reconciliation
- Sampling and disposal
- Finished product sales records
- Perpetual Inventory Records
- Reverse Distributor Manifest Forms (DEA Form 222 as applicable)
- Transfer Forms
- Yearly Reconciliation Summary Forms
- Support Aseptic Compounding and Filling teams throughout the manufacturing process:
- API check-out and transfer (electronic inventory) to PROD IN
- Return check-in of API and finished product
- Recording of consumption
- Finished product unit and reject count verification
- Line flush disposal
- Track and communicate batch release status (delays due to deviations/unplanned events), raw material availability, and inventory levels.
- Communicate with operations, post-production, and FSS Labs to request support as needed (e.g., VI and labeling, testing, and method validations).
- Execute all inventory reconciliation and expired inventory disposal activities.
- Maintain current electronic inventory in alignment with official paper records.
- Continuously monitor material accountability records for errors, completion of review, and verification signatures.
- Assist CS Compliance Management in preparing and submitting monthly/quarterly reports (e.g., ARCOS).
- Support operations by acting as a subject matter expert (SME) in ensuring DEA and site procedure compliance for all daily activities.
- Assist with the development and growth of a security culture among all colleagues and contractors to ensure CS compliance.
Requirements
- High School Diploma or equivalent required.
- Excellent time-management skills and ability to self-direct in managing concurrent requirements.
- Ability to communicate clearly and professionally with colleagues, customers, and suppliers in person, on the phone, and in writing.
- Excellent attention to detail and commitment to maintaining consistency and compliance with established procedures.
- Proactive, problem-solving mindset with the ability to identify and correct errors, offer improvement recommendations, and embrace ownership of complex processes.
- Must meet all requirements for handling controlled substances.
- Working knowledge of GDP principles as they relate to a pharmaceutical manufacturing environment.
- Previous work experience in a regulated manufacturing industry is a plus.
- Familiarity with and/or willingness to learn ERP system tracking and management.
Benefits
- Competitive salaries
- 401(k) plan with company matching contribution
- Medical, vision, and dental coverage
- Health Savings Account (HSA)
- Holiday and paid time off
At Fagron, you'll find plenty of opportunities for personal and professional growth. We work in an open, dynamic environment where your ideas and talents can shine.