Sterile Compounding Pharmacist (Part-time)

OurPharma LLCFayetteville, AR
Onsite

About The Position

OurPharma is looking for an individual to join our growing team as a part-time Sterile Compounding Pharmacist. This pharmacist will play a vital role in overseeing and/or participating in all aspects of the preparation and life cycle of sterile compounded products made in the 503B Outsourcing Facility. This position will work collaboratively with a team of pharmacists, technicians, & support personnel. You can be a part of the future of healthcare! OurPharma was founded to address pervasive pharmaceutical drug shortage problems in our nation's hospitals and medical clinics. Headquartered in Fayetteville, Arkansas, we pride ourselves on producing high-quality medications for healthcare organizations across the United States. With a multi-phase approach, OurPharma is set to grow our current footprint exponentially in the coming years with state-of-the-art facilities and equipment. As a company, we live and work by our core values: Integrity, Quality, Reliability, and Transparency. OurPharma is passionate about quality-driven initiatives that keep us transparent, reliable, and customer-focused.

Requirements

  • Demonstrated understanding of all policies and procedures relating to the function of this job position.
  • Adherence to current Good Manufacturing Practices (cGMPs) and Standard Operating Procedures.
  • Application of principles of aseptic/sterile compounding.
  • Proper hand washing, gloving, and gowning techniques.
  • Continuous inventory updates and audits of controlled substances.
  • Professional collaboration with intra- and inter-departmental staff.

Responsibilities

  • Participate in OurPharma's robust training program, which includes demonstration of understanding of all policies and procedures relating to the function of this job position.
  • Execute and/or supervise all processes associated with production of compounded sterile preparations while adhering to current Good Manufacturing Practices (cGMPs) and Standard Operating Procedures.
  • Apply principles of aseptic/sterile compounding in overseeing and/or participating in compounding of final drug products, media fills, stability studies and R&D batches.
  • Perform work in a sterile, cleanroom environment following proper hand washing, gloving, and gowning techniques.
  • Monitor/maintain drug inventories and assist in preparing orders for API and related supplies, including continuous inventory updates and audits of controlled substances.
  • Work collaboratively with intra- and inter-departmental staff in a professional manner.
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