Sterile Compounding Pharmacist

Chewy•Pittston, PA
•Onsite

About The Position

Chewy is seeking Sterile Compounding Pharmacists to support high-volume compounding operations at a 503A pharmacy in Pittston, Pennsylvania. The pharmacist oversees sterile compounding activities and helps ensure compliance with USP <795>, <797>, and <800>, applicable Board of Pharmacy regulations, and internal standards. The role balances clinical judgment, regulatory compliance, and production workflow oversight in a fast-paced environment, working collaboratively with pharmacists, technicians, quality personnel, and leadership to support safe and effective compounded sterile preparations (CSPs). The position also involves supervising and developing compounding personnel, maintaining cleanroom practices and documentation, supporting inspection readiness, and contributing to process improvement. Work takes place in a cleanroom and requires full garbing and PPE, with routine exposure to chemicals and hazardous drugs.

Requirements

  • Doctor of Pharmacy (PharmD) or Bachelor of Science in Pharmacy.
  • Active Pennsylvania pharmacist license.
  • At least 2 years of sterile compounding experience.
  • Strong working knowledge of USP <795>, USP <797>, USP <800>, aseptic technique, and cleanroom operations.
  • Ability to supervise and guide compounding personnel in a fast-paced setting.
  • Strong understanding of state and federal pharmacy laws and regulations.
  • Strong mathematical, analytical, and problem-solving skills.
  • Excellent attention to detail and commitment to patient safety and product quality.
  • Effective communication and collaboration skills across teams.
  • Willingness to complete ongoing training and competency assessments.
  • Ability to work in a cleanroom while wearing full garbing and PPE for extended periods.
  • Ability to undergo respirator fit testing; facial hair may interfere with a proper seal.
  • Ability to stand for prolonged periods and perform repetitive tasks.
  • Ability to lift at least 25 pounds with or without reasonable accommodation.
  • Ability to perform precise manipulations using small tools and equipment.
  • Ability to move frequently, including standing, walking, bending, reaching, and kneeling.
  • Ability to work with routine exposure to chemicals and hazardous drugs while strictly following safety protocols.
  • Ability to wear required compounding safety equipment, such as a gown, gloves, and respirator, for extended durations.

Nice To Haves

  • Experience in high-volume sterile compounding environments.
  • Experience with Category 2 and Category 3 sterile compounding.
  • Experience with electronic documentation systems and compounding workflow software.

Responsibilities

  • Oversee daily sterile compounding operations in the cleanroom and ensure compliance with USP <795>, <797>, and <800>, Board of Pharmacy regulations, and internal standards.
  • Apply clinical judgment to evaluate compounded preparations.
  • Perform and document sterile compounding procedures, including aseptic technique, environmental monitoring, and QA/QC checks.
  • Release compounded sterile preparations in accordance with regulatory and internal standards.
  • Supervise and direct pharmacy technicians and support personnel during compounding operations.
  • Train, assess, and maintain competency of compounding personnel, including media fills, gloved fingertip testing, and aseptic technique validation.
  • Maintain and enforce proper cleanroom behavior, garbing, and aseptic practices.
  • Oversee cleanroom workflow, daily logs, and environmental monitoring programs in collaboration with quality personnel.
  • Review and approve ingredients, supplies, and materials before their use in compounding.
  • Ensure proper calibration, maintenance, and use of compounding equipment.
  • Collaborate with quality, maintenance, and leadership teams to support operational efficiency and compliance.
  • Support process improvement initiatives to enhance workflow, throughput, and quality.
  • Ensure safe handling of hazardous drugs in accordance with USP <800> and applicable laws.
  • Maintain complete, accurate, inspection-ready documentation in electronic and/or manual systems.
  • Follow internal SOPs, regulatory requirements, and sterile compounding best practices.
  • Ensure a clean, sanitary, inspection-ready work environment and support audit and inspection readiness, including Boards of Pharmacy, PCAB, and NABP VPP.
  • Promote safety, accountability, and continuous improvement; maintain personal hygiene and dress appropriately to meet USP standards.
  • Perform other duties as assigned.
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