Pharmacist

Wells Pharma

Houston (TX)

On-site

USD 110,000 - 140,000

Full time

4 days ago
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Job summary

Wells Pharma is seeking a Pharmacist for a full-time, on-site role in Houston, TX. You will oversee sterile compounded medications, verify orders, ensure sterility and proper documentation, and maintain regulatory readiness.

You will collaborate with technicians, quality, and operations teams to promote safe practices, optimize workflows, and participate in QA activities while supporting investigations and ensuring patient safety.

Qualifications

  • Active Pharmacist license in good standing, eligible to practice in Texas.
  • Experience in sterile compounding, hospital pharmacy, or 503B outsourcing facilities preferred.
  • Knowledge of FDA 503B regulations, USP <797>/<800>, and cGMP or related quality standards.
  • Strong attention to detail and accuracy in order verification, documentation, and product review.
  • Ability to work collaboratively in a fast-paced, highly regulated environment.
  • Effective written and verbal communication skills and comfort with electronic health records or pharmacy systems.
  • Demonstrated commitment to patient safety, continuous improvement, and compliance with policies.
  • Doctor of Pharmacy (PharmD) or equivalent degree.

Responsibilities

  • Oversee the preparation, verification, and dispensing of sterile compounded medications.
  • Review and approve medication orders, verify formulations and labels.
  • Ensure accuracy, sterility, and proper documentation for all products.
  • Monitor compliance with USP standards and internal SOPs; participate in quality assurance activities.
  • Support investigations related to product quality or deviations.
  • Collaborate with pharmacy technicians, quality teams, and operations staff to promote safe practices and optimize workflows.
  • Provide training to team members and contribute to process improvements.
  • Communicate with internal stakeholders regarding product status and inventory needs.

Skills

Attention to detail
Communication skills
Collaboration
Regulatory compliance

Education

PharmD or equivalent

Tools

Pharmacy systems

Job description

Company Description

Wells Pharma is a registered FDA 503B Outsourcing Facility that provides medications to hospitals and surgical centers nationwide. The organization is focused on supplying high-quality sterile products that support safe and effective patient care. Wells Pharma emphasizes reliability, regulatory compliance, and adherence to rigorous quality standards in all manufacturing processes. Team members are encouraged to contribute to a culture of excellence, collaboration, and continuous improvement. The company is committed to delivering industry-leading customer service and building long-term relationships with healthcare partners.

Role Description

The Pharmacist is a full-time, on-site role based in Houston, TX, responsible for overseeing the preparation, verification, and dispensing of sterile compounded medications in accordance with FDA 503B and applicable regulatory guidelines. Day-to-day responsibilities include reviewing and approving medication orders, verifying formulations and labels, and ensuring accuracy, sterility, and proper documentation for all products. The role involves monitoring compliance with USP standards and internal SOPs, participating in quality assurance activities, and supporting investigations related to product quality or deviations. The Pharmacist collaborates with pharmacy technicians, quality teams, and operations staff to promote safe practices, optimize workflows, and maintain regulatory readiness. Additional tasks may include training team members, contributing to process improvements, and communicating with internal stakeholders regarding product status and inventory needs.

Qualifications
  • Active Pharmacist license in good standing, with eligibility to practice in Texas.
  • Experience in sterile compounding, hospital pharmacy, or 503B outsourcing facilities is strongly preferred.
  • Knowledge of FDA 503B regulations, USP <797>/<800>, and cGMP or related quality and safety standards.
  • Strong attention to detail and accuracy in order verification, documentation, and product review.
  • Ability to work collaboratively in a fast-paced, highly regulated environment and support cross-functional teams.
  • Effective written and verbal communication skills and comfort with electronic health records or pharmacy systems.
  • Demonstrated commitment to patient safety, continuous improvement, and compliance with policies and procedures.
  • Doctor of Pharmacy (PharmD) or equivalent degree;
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