Lead Sterile Pharmacist

Description Key Responsibilities Serve as a 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. Skills Pharmacy, Rph, Pharmd, Compounding, Lead Top Skills Details Pharmacy,Rph,Pharmd Additional Skills & Qualifications Required Qualifications Doctor 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. Preferred Qualifications Experience 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. Experience Level Intermediate Level Job Type & Location This is a Permanent position based out of Johnstown, OH. Pay and Benefits The pay range for this position is $140000.00 - $149760.00/yr. Competitive pay with shift differentials for qualifying schedules Medical, dental, and vision insurance 401(k) retirement plan with employer contribution Paid time off and paid holidays Continuing education and professional development support Safe, modern work environment with a strong focus on compliance and quality Workplace Type This is a fully onsite position in Johnstown,OH. Application Deadline This position is anticipated to close on May 14, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people Actalent is an equal opportunity employer. About Actalent Actalent is a global leader in engineering and sciences services. For more than 40 years, we've helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.