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Quality Assurance Pharmacist - Night Shift

Job in Houston, Harris County, Texas, 77001, USA
Listing for: Southend Pharmacy
Full Time position
Listed on 2026-08-30
Job specializations:
  • Healthcare
    Healthcare Compliance
Job Description & How to Apply Below
Position: Quality Assurance Pharmacist - Night Shift (10PM - 6AM)

Lead Pharmacist

Southend Pharmacy, a subsidiary of Allia Health Group, is a rapidly growing 503A compounding pharmacy committed to delivering safe, high-quality, patient-centered care. Our pharmacy specializes in sterile and non-sterile compounded medications, clinical excellence, and innovative pharmacy solutions that support providers and patients nationwide. As demand grows, we are expanding our onsite leadership team and seeking a highly skilled Lead Pharmacist to support daily operations, uphold regulatory standards, and elevate our compounding practice.

Quality

Assurance (QA) Pharmacist

The Quality Assurance (QA) Pharmacist plays a critical role in ensuring compliance with applicable regulations, compounding standards, and internal procedures in a 503A compounding pharmacy. This position is responsible for maintaining the integrity of compounded preparations through oversight of quality systems, documentation, and continuous improvement practices. The QA Pharmacist will work collaboratively with pharmacy staff to ensure patient safety, product quality, and regulatory compliance.

Key Responsibilities

  • Develop, implement, and maintain QA systems in alignment with USP 795, 797, 800, state board of pharmacy regulations, and other applicable standards
  • Monitor, document, and investigate reported adverse events or product complaints and ensure timely reporting to appropriate regulatory bodies, and implement follow-up actions including root cause analysis, trending, and corrective measures in accordance with pharmacy policies and applicable laws
  • Conduct and/or oversee routine audits of sterile and non-sterile compounding processes, facilities, equipment, and documentation
  • Review and approve compounding records, batch release documents, and standard operating procedures (SOPs)
  • Investigate deviations, non-conformances, and out-of-specification results; lead root cause analysis and ensure appropriate corrective and preventive actions (CAPAs)
  • Oversee and ensure proper handling, storage, and qualification of raw materials and components
  • Conduct risk assessments to evaluate and mitigate potential quality or compliance issues
  • Coordinate and respond to quality-related inspections by state or federal agencies
  • Maintain records in compliance with documentation requirements
  • Support change control, validation, and qualification efforts related to new processes, products, or equipment

Qualifications

  • Education:

    Doctor of Pharmacy (PharmD) or Bachelor of Science in Pharmacy from an accredited institution
  • Licensure:
    Active pharmacist license in good standing with the Texas State Board of Pharmacy (multistate licensure is a plus)
  • Experience:

    Minimum of 1-2 years of experience in sterile compounding, preferably in a 503A pharmacy, with a strong understanding of USP 797, 795, 800 and cGMP standards; 1+ year in a quality assurance or compliance-related role preferred
  • Skills:

    In-depth knowledge of sterile compounding techniques, aseptic processing, and quality assurance principles; strong analytical and problem-solving skills to investigate deviations and implement effective solutions; excellent attention to detail and organizational skills to manage complex documentation and compliance requirements; effective communication and training skills to educate staff and collaborate with cross-functional teams; proficiency in pharmacy information systems and quality management software; ability to train and mentor team members on quality systems and compliance
  • Physical Requirements:

    This role requires routine presence in cleanroom and laboratory environments. May involve standing, gowning, and working in controlled environments for extended periods

Physical Requirements

  • Ability to sit for extended periods of time at a desk and working on a computer
  • Ability to communicate effectively in person, over the phone, or via virtual meeting
  • Ability to maintain focus in a typical office environment with moderate noise levels
  • This role requires routine presence in cleanroom and laboratory environments
  • May involve standing, gowning, and working in controlled environments for extended periods

What We Offer

  • Full benefits package including medical, vision, dental,…
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