STAQ Pharma is currently hiring for a quality control technician to join our team here in Columbus
Shift: Monday to Friday, 8 AM to 4:30 PM

STAQ Pharma:

• Safety, Transparency, Availability, and Quality.
• FDA Registered 503B Outsourcing Facility that produces sterile injectable medications for adult and pediatric patients, compounded under Current Good Manufacturing Practices (cGMP) standards.
• Facilities in Columbus, Ohio and in Denver, Colorado.
• Regulated by the FDA, DEA, and all State Boards of Pharmacy.
  
  
  Quality Control Technician is responsible for:
• Ensuring compliance with cGMP requirements and company procedures.
• Providing QC Support throughout all departments.
• Coordinating QC sample preparation and external laboratory shipments.
• Assisting with Environmental Monitoring activities.
  Roles and Responsibilities
• Maintain retention materials and disposal when required.
• Assist with review and release of raw materials, API, excipients, and sterile supplies.
• Coordination of Biohazard waste destruction.
• Perform sampling and inspection of in-process and finished products.
• Assists with Environmental Monitoring activities.
• Logbook and controlled document generation.
• Assist with investigations and develop and implement corrective and preventive actions geared toward continuous process improvements.
• Review GMP documents including master batch production records, room and equipment logs, etc.
• Support quality management system activities including document control and training program management.
• 1-3 years as a Quality Technician.
• Other duties and tasks, as assigned.
  
  
  Qualifications and Education Requirements
  Must be able to read and write in English
• Pharmaceutical, Medical Device industry, or biotechnology experience, preferably in support of manufacturing.
• Associate degree in the sciences or equivalent experience preferred.
  Preferred Skills
• Excellent independent judgement, written communication, verbal communication, and interpersonal skills.
• Strong attention to detail.
• Familiarity with Good Manufacturing Practices and FDA Regulations.
• Proficient in using Microsoft Word, Excel, PowerPoint, Outlook.
  Additional Notes
  This position will work closely with the Production team and report quality data to department management, as needed.