Careers

Are you looking for a career in an innovative start up? STASKA Pharmaceuticals is looking for positive, driven, and detail-oriented individuals with a problem-solving mindset. Our newly designed outsourcing facility offers sterile products to a variety of healthcare providers and offices. You can play a vital role in enhancing pharmaceutical supply for patients and providers. View the positions below and apply!

Competitive Wages Flexible Schedule Competitive Benefits

Open Positions

Aseptic Compounding TechnicianFull-time · Mon–Fri day shift · Bennet, NE

About the role

STASKA Pharmaceuticals is an FDA-registered 503B outsourcing facility specializing in the compounding of high-quality sterile medications. We are seeking detail-oriented individuals who are committed to patient safety, quality, and operational excellence.

The Aseptic Compounding Technician plays a critical role in the preparation, compounding, and packaging of sterile pharmaceutical products. This position operates within controlled cleanroom environments and follows established quality systems and current Good Manufacturing Practices (cGMP).

Responsibilities

  • Perform aseptic compounding activities in accordance with approved procedures and cGMP requirements.
  • Maintain cleanroom environments through proper gowning, cleaning, sanitization, and contamination control practices.
  • Prepare, sterilize, and assemble components required for sterile compounding operations.
  • Operate compounding and processing equipment according to approved procedures.
  • Complete production documentation, batch records, equipment logs, and cleaning records accurately and contemporaneously.
  • Stage and verify materials required for scheduled compounding activities.
  • Ensure components and materials meet established requirements before use.
  • Perform visual inspections and assist with packaging and labeling operations.
  • Participate in environmental monitoring, training, qualification, and aseptic process simulation activities.
  • Identify and report quality concerns, deviations, and opportunities for process improvement.
  • Support a culture focused on patient safety, quality, compliance, and continuous improvement.

Qualifications

  • High school diploma or equivalent required.
  • Experience in pharmaceutical compounding, sterile compounding, hospital IV preparation, medical device manufacturing, or other regulated production environments preferred.
  • Strong attention to detail and ability to follow written procedures precisely.
  • Ability to work in a cleanroom environment while wearing required personal protective equipment.
  • Strong documentation and organizational skills.
  • Ability to work effectively in a team-oriented compounding environment.
  • Previous cGMP experience preferred but not required.
Job typeFull-time
ScheduleMonday–Friday, day shift, no weekends
BenefitsHealth insurance, paid time off, professional growth

Apply online

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