Compounding Pharmacist

AVEVA DRUG DELIVERY SYSTEMS INC•Tamarac, FL

23h•Onsite

About The Position

Aveva Drug Delivery Systems is a pharmaceutical manufacturer at the forefront of innovative drug delivery technologies. We are dedicated to advancing solutions that optimize the efficacy, safety, and precision of pharmaceutical treatments. Join our team and help shape the future of healthcare by contributing to the development of groundbreaking drug delivery systems that improve patient outcomes worldwide.

Requirements

Bachelor’s or Doctor of Pharmacy (PharmD) degree from an accredited institution.
Must hold an active Registered Pharmacist license in the State of Florida.
Minimum of 3 years of experience in pharmaceutical compounding or sterile manufacturing.
Strong understanding of cGMP, 503(b) outsourcing regulations, FDA guidelines, aseptic/sterile compounding principles, USP 797 & USP 800.
Familiarity with environmental monitoring, gowning, and aseptic techniques in controlled manufacturing environments.
Excellent organizational, communication, and leadership skills.
Proficiency in reviewing and maintaining documentation, including batch records and SOPs.
Strong problem-solving skills and attention to detail.

Nice To Haves

Preferred active Registered Pharmacist license in multistate.
Experience with 503(b) outsourcing facilities and aseptic/terminal sterilization processes preferred.
Preferred BCSCP (Board Certified Sterile Compounding Pharmacist) by BPS (Board of Pharmacy Specialties).

Responsibilities

Directly supervise and oversee 503(b) compounding operations, including aseptic processing and terminal sterilization activities.
Ensure adherence to batch production records (BPRs) and standard operating procedures (SOPs).
Monitor production activities to maintain compliance with cGMP, FDA 503(b) outsourcing facility regulations, and State of Florida pharmacy board requirements.
Ensure all operations comply with applicable state and federal pharmacy laws and FDA regulations.
Maintain the pharmacy license and ensure all processes meet Florida Board of Pharmacy standards.
Conduct regular documentation reviews and approve production batch records to ensure completeness and accuracy.
Collaborate with the Quality Assurance (QA) team to ensure that compounded and terminally sterilized pharmaceuticals meet quality and safety standards.
Participate in quality investigations, deviations, corrective and preventive actions (CAPAs), and audits.
Support validation activities, including aseptic process simulations (media fills) and sterilization process validations.
Provide leadership, training, and technical support to compounding technicians and other personnel.
Ensure all staff are trained and competent to perform duties in compliance with GMP and regulatory requirements.
Foster a culture of continuous improvement, safety, and quality.
Monitor and ensure accurate labeling, documentation, and traceability of compounded products.
Collaborate with supply chain and production teams to manage inventory of raw materials, consumables, and sterile components.
Assist with process improvements to optimize production efficiency while maintaining compliance and quality standards.