Staq Pharma Jobs Hiring Now
Staq Pharma is hiring for 7 open roles on Migrate Mate as of July 16, 2026, concentrated in manufacturing operations and business analysis. Migrate Mate updates Staq Pharma's live openings daily. Staq Pharma is a pharmaceutical company hiring across quality, operations, HR, and technical support functions.
Find Staq Pharma JobsOverview
Staq Pharma hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 7
- Top team
- Manufacturing Operations
- Seniority
- Across all levels
- Work type
- 0% remote or hybrid
- Top location
- Denver
Open Roles at Staq Pharma
Showing 7 of 7+ Staq Pharma jobs
Job Summary:
Quality Control Microbiology Technician 1 will provide clean room support for batch production and ensuring procedure adherence during filling of product. Utilize appropriate controlled documents and assist in quality control deviations/investigations.
Responsibilities:
- Ensure clean rooms and associated areas meet the required cleanliness standards as per company procedures.
-
Adhere to strict gowning and personal hygiene practices to prevent contamination and maintain integrity of the clean room environment.
- Perform gowning qualification training for individuals from all departments who must enter ISO 7 classified areas.
-
Monitor and maintain clean room equipment such as viable and non-viable samplers to ensure optimal performance and compliance with established standards.
- Perform and lead routine environmental monitoring activity in ISO 7 Classified Areas
- Work with production to resolve Quality issues and ensure documentation is complete.
- Perform routine and non-routine viable, non-viable and surface environmental monitoring in all classified areas of the facility.
-
Incubation and enumeration of samples related to environmental monitoring processes.
- Train new personnel on enumeration activities
-
Evaluate organisms by colony morphology and perform subculturing.
- Train new personnel on colony morphology assessment and subculturing activities.
- Perform and/or verify gram stain testing morphology results.
- Continuous improvement activities for environmental monitoring program.
- Provide quality control and microbiology support for operations.
- Collect, submit and manage microbiological samples to third party testing laboratories.
- Assist with QC Microbiologists (and other investigators) with investigations as they relate to environmental monitoring or other quality control deviations.
- Assist QC Microbiologists with data trending and data reporting as they relate to environmental monitoring or other data-generating processes.
-
Perform routine testing or cleaning associated with the BioSafety Cabinet.
- Lead and train new personnel on the cleaning procedures and testing procedures carried out in the BioSafety Cabinet
- Assist in process, procedural, equipment issues via experimentation or revision of procedures.
- Other duties as assigned.
Required Skills/Abilities: (examples)
- Experience with cGMP aseptic manufacturing environment.
- Strong attention to detail.
- Comfortable in a fast-paced, small company environment and able to adjust workload based upon changing priorities.
- Preferred previous pharmaceutical experience.
- Proficient in using Microsoft Word, Excel, PowerPoint, Outlook.
- Familiarity with 21 CFR Part 11/210/211
Education and Experience:
- Associate or Bachelor’s degree in Microbiology, Biology, or related life sciences.
- Experience in microbiology or quality control preferred.
- Experience in a cGMP or cleanroom setting preferred.
Physical Requirements:
- Prolonged periods of sitting at a desk or laboratory bench and working on a computer.
- Must be able to lift up to 15 pounds at times.
The application window for this position is anticipated to be open at least 25 days
Job Summary:
Quality Control Microbiology Technician 1 will provide clean room support for batch production and ensuring procedure adherence during filling of product. Utilize appropriate controlled documents and assist in quality control deviations/investigations.
Responsibilities:
- Ensure clean rooms and associated areas meet the required cleanliness standards as per company procedures.
-
Adhere to strict gowning and personal hygiene practices to prevent contamination and maintain integrity of the clean room environment.
- Perform gowning qualification training for individuals from all departments who must enter ISO 7 classified areas.
-
Monitor and maintain clean room equipment such as viable and non-viable samplers to ensure optimal performance and compliance with established standards.
- Perform and lead routine environmental monitoring activity in ISO 7 Classified Areas
- Work with production to resolve Quality issues and ensure documentation is complete.
- Perform routine and non-routine viable, non-viable and surface environmental monitoring in all classified areas of the facility.
-
Incubation and enumeration of samples related to environmental monitoring processes.
- Train new personnel on enumeration activities
-
Evaluate organisms by colony morphology and perform subculturing.
- Train new personnel on colony morphology assessment and subculturing activities.
- Perform and/or verify gram stain testing morphology results.
- Continuous improvement activities for environmental monitoring program.
- Provide quality control and microbiology support for operations.
- Collect, submit and manage microbiological samples to third party testing laboratories.
- Assist with QC Microbiologists (and other investigators) with investigations as they relate to environmental monitoring or other quality control deviations.
- Assist QC Microbiologists with data trending and data reporting as they relate to environmental monitoring or other data-generating processes.
-
Perform routine testing or cleaning associated with the BioSafety Cabinet.
- Lead and train new personnel on the cleaning procedures and testing procedures carried out in the BioSafety Cabinet
- Assist in process, procedural, equipment issues via experimentation or revision of procedures.
- Other duties as assigned.
Required Skills/Abilities: (examples)
- Experience with cGMP aseptic manufacturing environment.
- Strong attention to detail.
- Comfortable in a fast-paced, small company environment and able to adjust workload based upon changing priorities.
- Preferred previous pharmaceutical experience.
- Proficient in using Microsoft Word, Excel, PowerPoint, Outlook.
- Familiarity with 21 CFR Part 11/210/211
Education and Experience:
- Associate or Bachelor’s degree in Microbiology, Biology, or related life sciences.
- Experience in microbiology or quality control preferred.
- Experience in a cGMP or cleanroom setting preferred.
Physical Requirements:
- Prolonged periods of sitting at a desk or laboratory bench and working on a computer.
- Must be able to lift up to 15 pounds at times.
The application window for this position is anticipated to be open at least 25 days
Job Roles at Staq Pharma
Working at Staq Pharma
Staq Pharma's 7 open roles are across all levels, and about 0% are remote or hybrid. The most active teams are manufacturing operations, business analysis, and data analytics. Staq Pharma is a pharmaceutical company with open positions spanning quality assurance, quality control, formulation, HR, IT, and training and development. The company operates in the pharmaceutical manufacturing and compounding sector, with roles that support both laboratory operations and business functions. Most Staq Pharma roles are based in Denver and Columbus.
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Browse jobs by roleStaq Pharma Jobs: Frequently Asked Questions
How many jobs is Staq Pharma hiring for right now?
Staq Pharma is hiring for 7 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in manufacturing operations and business analysis. Open positions have included quality assurance, formulation, IT helpdesk, HR, and training roles across the organization.
What kinds of roles does Staq Pharma hire for?
The most active teams are manufacturing operations, business analysis, and data analytics. Staq Pharma's open positions span quality assurance, quality control, laboratory and formulation work, HR business partnering, IT support, and training and development. Most postings are across all levels, covering both technical laboratory roles and operational or administrative positions.
Are Staq Pharma jobs remote or in-person?
Mostly on-site. About 0% of Staq Pharma's open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in Denver. Each Staq Pharma listing shows its work location so you can filter before applying.
How do I apply to a job at Staq Pharma?
Find a Staq Pharma role you want on Migrate Mate, then follow the listing through to Staq Pharma's own application page. Staq Pharma manages its own hiring process, including application review and interviews, so you apply and communicate directly with the company.
Does Staq Pharma hire entry-level?
Most of Staq Pharma's open roles on Migrate Mate are across all levels as of July 16, 2026. Check individual Staq Pharma listings for stated experience requirements.
Where is Staq Pharma hiring?
Most Staq Pharma roles are based in Denver and Columbus, and about 0% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.