COMPANY OVERVIEW

Before we opened Strive Pharmacy we were unsatisfied with the current state of the pharmaceutical industry. Most of the current pharmaceuticals only offer a one size fits all approach and often come with unwanted and potentially dangerous side effects. We found that through compounding we can offer a much more personalized solution to medicine.
Through this we have been able to help patients get the results they are seeking for their personal needs. After years of working for corporate chains we took the risk and opened Strive Pharmacy. We are dedicated to providing a better experience for each customer and clinic that we work with. Come see the Strive difference.

POSITION OVERVIEW

Ensure and assist with site-specific quality compliance according to Strive Pharmacy SOPs & specifications; quality review of documents, label control, assist with release activities and product inspections.

DESIRED SKILLS

• Experienced in aseptic operations
• Experience within a regulated environment
• Knowledge & skills in Pharmaceutical Quality Assurance Practices
• Associates Degree or higher level degree in technician technical scientific discipline; Biology, Microbiology, Chemistry, or Pharmacy
• Strong organizational skills and attention to detail
• Ability to effectively troubleshoot issues
• Comfortable working in a cleanroom-working environment that may be limited to a small area, wearing protective cleanroom attire, tolerating controlled temperatures, and loud noise

REQUIRED QUALIFICATIONS

• Minimum of High School Diploma/GED with work experience
• Minimum of 2 years experience in a quality or manufacturing department of a Pharmaceutical, Medical Device, or Allied Health Science.

• Perform product inspection for defects, leaks, and particulates
• Environmental monitoring of personnel (as needed) and complete documentation
• Assist in the media fill process validations to include inspection of filled units
• Perform documentation review of compounding activities such as cleaning records, line clearance forms, and inventory sheets:
• Verify that raw materials meet specification
• Account for labeling
• Review temperature and BMS alarms
• Ensure that product test results meet specification limits
• Checking that all documentation is complete
• Document non-compliance and work with supervisor/lead if further investigation is needed appropriate lab for particulate identification or microbial analysis
• Help with equipment calibration program and maintenance record files
• Assist with raw material release and movement
• Under the direction of supervisor/lead, document and initiate quality events for deviation and noncompliant investigations
• Support internal & external audits
• Maintain quality records (equipment calibration and maintenance, training, deviation and compliant investigation, environmental monitoring, certificate of analysis, clean room certification etc.)
• Participate in Quality Manager’s staff meetings