Assistant to Operations Manager - Full Time

Compounding Operations Supervisor ( Job Number: 26001987)
Pharma
Employee Type : Full-Time
Pay Rate From : $92,900 CAD
Pay Rate To : $120,000 CAD
Under the direct supervision of Manager, Sterile Compounding, the Supervisor, Compounding Operations is responsible for overseeing daily operations of the Drug Preparation Premises (DPP), including workflow management, staff supervision, and ensuring compliance with all regulatory, professional, and organizational standards.
The Compounding Operations Supervisor provides leadership and supervision to pharmacists, pharmacy technicians, assistants, clerks and support staff involved in sterile compounding operations both inside and outside the cleanroom environment. Oversees daily workflow and production activities within the Drug Preparation Premises (DPP), ensuring operational efficiency and compliance with regulatory requirements.
Ensures adequate staffing coverage by preparing staff schedules, managing sick calls, and coordinating staffing adjustments as required.
Provides day-to-day supervision, coaching, and guidance to team members to ensure high standards of performance and professionalism.
Participates in staff performance evaluations and provides feedback to support employee development and performance improvement.
Supports onboarding, orientation, and training of new employees within compounding operations.
Identifies staff training needs and supports competency assessments in collaboration with management.
Promotes a culture of safety, accountability, teamwork, and continuous improvement.
Monitor cleanroom activities to ensure aseptic technique, environmental controls, and sterile compounding practices are consistently followed.
Ensures appropriate cleaning and disinfection of controlled areas, equipment, and facilities. ensuring compliance with SOPs and regulatory requirements
Ensures all sterile preparations are compounded, labeled, verified, packaged, and dispensed in accordance with regulatory and professional standards.
Oversees and supports environmental monitoring programs including air and surface sampling in cleanroom and anteroom areas.
Coordinates and supports glove fingertip testing and media fill testing for compounding personnel.
Supports sterility testing programs and ensures documentation accuracy including Certificates of Analysis.
Oversees medication and supply inventory including ordering, receiving, storage, and expiry monitoring.
Oversees dispensing and shipping schedules to ensure timely and accurate order fulfillment.
Participates in internal meetings, audits, and third-party inspections as required.
Contributes to the development, review, and improvement of SOPs, policies, and operational workflows.
Ensures accurate and compliant packaging and dispensing of final sterile preparations, including:
o Verifying accuracy and completeness of compounded sterile products
o Ensuring preparations are correctly matched to delivery schedules for timely shipping
Supports the Drug Preparation Premises (DPP) Manager and Sterile Compounding Supervisor in maintaining compliance with federal, provincial, and local regulations, and accreditation standards.
Ensures adherence to all applicable SOPs, quality standards, and regulatory requirements, including those of the Ontario College of Pharmacists.
Accountable for daily operational outcomes within sterile compounding activities, including production throughput, quality standards, and regulatory compliance for assigned shifts.
Holds decision making authority within scope to address workflow disruptions, staffing variances, and operational risks, taking timely corrective action and escalating only when required.
Bachelor of Pharmacy (BPharm) from an accredited institution is required.
Demonstrated working knowledge of applicable regulatory and professional standards , including OCP requirements, NAPRA Model Standards, and relevant federal and provincial legislation governing sterile compounding.
Proven ability to lead within a regulated cleanroom environment , including adherence to aseptic technique, environmental controls, documentation standards, and quality assurance practices, is preferred