STAQ Pharma is currently hiring for quality control technicians to join our team in the Denver Metro area.
Schedule: Monday to Friday, 12 PM to 8:30 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. • Headquartered in Denver, Colorado and an additional facility in Columbus, Ohio. • State-of-the-art facilities and commitment to automation for preparation of ready to administer pharmaceutical products in syringes, pumps, bags, etc. • 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. • Coordinating QC sample preparation and external laboratory shipments. • Providing QC support throughout all departments.
Responsibilities for Quality Control Specialist include: • Works effectively and efficiently in a team environment. • Assist review and release of raw materials, API, excipients, and sterile supplies. • Demonstrates the ability to perform detail-oriented work with a high degree of accuracy. • Maintain retention materials and disposal when required. • Logbook and controlled document generation. • Coordination of Biohazard waste destruction. • Perform safety equipment checks. • Assist with the development, management and improvement of quality system processes and procedures to ensure compliance with applicable laws, regulations, and company standards in support of cGMP for pharmaceutical compounding. • Perform sampling and inspection of in-process and finished products. • Assist with investigations and develop and implement corrective and preventive actions geared toward continuous process improvements. • Perform evaluations to determine effectiveness of corrective actions. • Performs other duties as assigned.
Preferred Skills • Previous pharmaceutical experience. • Experience with aseptic manufacturing environments. • Comfortable in a fast-paced, small company environment and able to adjust workload based upon changing priorities. • Excellent independent judgement and interpersonal skills. • Strong attention to detail. • Excellent written and verbal communication skills. • 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.