Qureos Mentor

Staq Pharma

<div><h3 class="jobSectionHeader">Company Overview &ndash; STAQ Pharma</h3>
STAQ Pharma is an FDA-registered 503B outsourcing facility dedicated to producing high-quality, sterile injectable medications for both adult and pediatric patients. All products are compounded under Current Good Manufacturing Practices (cGMP) standards.<ul><li>
Headquartered in Denver, Colorado with an additional facility in Columbus, Ohio</li><li>
Regulated by the FDA, DEA, and State Boards of Pharmacy</li><li>
Committed to Safety, Transparency, Availability, and Quality</li><li>
Equipped with state-of-the-art facilities and advanced automation to support the preparation of ready-to-administer pharmaceuticals (syringes, pumps, bags, etc.)</li></ul><h3 class="jobSectionHeader">
Position Summary</h3>
The Quality Control Microbiology Technician supports STAQ Pharma&rsquo;s environmental monitoring program and ensures compliance with cGMP standards and internal procedures. This role plays a key part in maintaining the integrity of cleanroom operations and supporting microbiological testing efforts across the facility.
Schedule: Monday to Friday, 2pm-10:30pm 
However, in the event of a production delay, the employee is expected to remain on-site to support operations until production is complete.<h3 class="jobSectionHeader">
Key Responsibilities</h3><ul><li>
Conduct viable and non-viable environmental monitoring (EM) of all classified cleanroom areas</li><li>
Perform surface sampling, active air, and passive air sampling according to SOPs</li><li>
Incubate and enumerate environmental monitoring samples</li><li>
Conduct morphology assessments following incubation</li><li>
Perform microbiological testing including gram stains, subculturing, and microorganism identification</li><li>
Maintain and monitor EM equipment (viable and non-viable samplers) for proper function</li><li>
Follow proper gowning and hygiene procedures to prevent contamination</li><li>
Work cross-functionally with production teams to resolve quality concerns and ensure complete, compliant documentation</li><li>
Support investigations related to environmental monitoring deviations or other quality issues</li><li>
Assist with continuous improvement initiatives within the EM program</li><li>
Submit and manage samples for third-party microbiological testing</li><li>
Participate in procedural reviews, equipment troubleshooting, and SOP revisions</li><li>
Perform other duties as assigned</li></ul><h3 class="jobSectionHeader">
Qualifications</h3>
Education:<ul><li>
Bachelor&rsquo;s degree in Microbiology or a closely related scientific field</li></ul>
Required Skills &amp; Competencies:<ul><li>
Strong organizational and communication skills</li><li>
Ability to follow strict cGMP and aseptic techniques</li><li>
Strong attention to detail</li></ul>
Preferred Experience:<ul><li>
Prior experience in a cGMP-regulated aseptic manufacturing environment</li><li>
Pharmaceutical or biotechnology industry background</li><li>
Familiarity with 21 CFR Part 11, 210, and 211 regulations</li><li>
Proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook)</li><li>
Comfortable working in a fast-paced, dynamic environment with shifting priorities</li></ul><h3 class="jobSectionHeader">
Additional Notes</h3>
This position works closely with Operations and Quality leadership to support microbiological data collection and reporting efforts.</div>

Quality Control Microbiology Technician

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Staq Pharma

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Quality Control Microbiology Technician