STAQ Pharma is currently hiring for a quality control technician to join our team here in Columbus
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.
- Summary
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.