Job Title: Lead Sterile PharmacistJob Description

We are seeking a dedicated and skilled Lead Sterile Pharmacist to oversee the compounding of sterile preparations and ensure compliance with USP and USP standards. This role involves managing and training personnel, enforcing proper aseptic techniques, and collaborating with development teams to innovate and improve compounding processes.

ResponsibilitiesServe as the designated responsible person for USP and USP compliance, as assigned by sterile compounding leadership.Oversee and enforce proper aseptic technique, cleanroom behavior, and workflow controls.Train, supervise, and support pharmacists, technicians, and support personnel performing sterile and pre-sterilization activities.Perform and accurately document compounding procedures, quality assurance, and quality control checks for compounded sterile preparations.Review and approve materials, components, and supplies prior to use in sterile compounding.Oversee sterile compounding equipment and coordinate environmental controls in partnership with maintenance teams.Manage cleanroom documentation, daily logs, and environmental monitoring activities in collaboration with quality personnel.Provide direct leadership for day-to-day sterile compounding execution, including staffing, workflow oversight, and issue resolution.Collaborate with development teams on the introduction, validation, and scale-up of new compounded sterile preparations.Ensure compliance with all safety requirements, USP standards, Board of Pharmacy regulations, FDA requirements, and internal procedures.Promote a safety-first culture, including proper handling of hazardous drugs in accordance with USP .Wear required personal protective equipment (PPE) as necessary for compounding and cleanroom activities.Partner with the Pharmacist-in-Charge and sterile compounding leadership on personnel, quality, compliance, and regulatory matters.Complete required training and maintain ongoing competency.Essential SkillsDoctor of Pharmacy (PharmD) or Bachelor of Pharmacy degree from an accredited institution.Active, unrestricted Pharmacist license in the state of employment (OH or AZ).Minimum of 3 years of pharmacist experience.At least 1 year of hands-on sterile compounding experience; experience compounding from non-sterile starting components preferred.Strong working knowledge of USP and USP requirements and best practices.Current knowledge of state and federal pharmacy laws and regulations.Prior experience in a leadership or supervisory role.Ability to work flexible schedules, including overnight shifts.Proficiency with Windows-based computer systems.Ability to complete respirator fit testing (facial hair may interfere with proper fit).Demonstrated ability to lead with professionalism, empathy, and accountability in an in-person pharmacy setting.Ability to lift at least 25 pounds with or without reasonable accommodation.Ability to stand and perform physical tasks for extended periods, including walking, bending, reaching, and kneeling.Ability to wear required sterile compounding safety equipment for prolonged periods.Commitment to protecting patient information and complying with HIPAA and PHI requirements.Ability to maintain a clean, sanitary, and inspection-ready environment in accordance with FDA and regulatory standards.Additional Skills & QualificationsExperience compounding sterile preparations from non-sterile starting components.Familiarity with electronic documentation systems and compounding workflow software.Experience supporting or leading regulatory inspections (e.g., State Board of Pharmacy, FDA, NABP).One or more years of direct management experience overseeing pharmacists, technicians, or pharmacy support staff.Work Environment

This role operates in a pharmaceutical manufacturing environment with a closed-door pharmacy feel. The shift follows a 6pm-6am 3-2-2-3 schedule, offering flexibility in days on and off, dependent on other candidates.

Job Type & Location

This is a Permanent position based out of Columbus, OH.

Pay and Benefits

The pay range for this position is $139000.00 - $139360.00/yr.

Competitive pay with shift differentials for qualifying schedulesMedical, dental, and vision insurance401(k) retirement plan with employer contributionPaid time off and paid holidaysContinuing education and professional development supportSafe, modern work environment with a strong focus on compliance and quality

Workplace Type

This is a fully onsite position in Columbus,OH.

Application Deadline

This position is anticipated to close on Feb 18, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.