Associate Director Clinical Quality Assurance Jobs in Colorado
Associate Director Clinical Quality Assurance jobs in Colorado are concentrated in Denver, Boulder, and the Denver Tech Center corridor, where established life sciences companies, contract research organizations, and pharmaceutical manufacturers maintain significant quality and regulatory operations. Employers such as Davita, Envision Healthcare, and UCHealth regularly hire at this level, alongside a growing cluster of biotech and CRO firms along the Front Range. The most in-demand specialties include GCP auditing, clinical trial quality oversight, and regulatory submissions compliance. Find a role that fits below and apply directly.
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Job Title: Technical Services Technician
Reports to: Technical Services Supervisor
Summary: The Quality Assurance Technician monitors production processes of the facility to ensure all products meet company food safety and quality requirements as set forth by company policies, customer requirements, USDA and BRC standards.
Essential Duties and Responsibilities
- Complies with all food safety and quality policies, USDA regulations and BRC third party requirements. Models and coaches these expectations to other employees.
- Ensures product meets internal and customer specifications and takes appropriate actions when a non-compliance issue is noted.
- Conducts product audits for compliance to include (but not limited to) proper labeling, packaging, temperature, product specifications, and weights.
- Performs and records quality checks on product and regulatory checks as specified within company HACCP, food safety and quality programs and USDA regulations.
- Inspects equipment for cleanliness and proper working condition prior to start up and record findings. Collects microbiological pre-op swabs.
- Conducts raw material audits to ensure incoming products are within specification before production.
Education/Experience:
- Preferably a high school diploma or equivalent, and one (1) years’ experience in a manufacturing setting, preferably in a food-processing environment.
- Excellent reading, communication, and organizational skills. Ability to add, subtract, multiply, and divide units of U.S. currency, weight, volume, and distance measurements, etc.
- Must be able to prioritize projects and multitask.
- Ability to read and comprehend simple instructions, short correspondence, and memos. Ability to read and interpret documents and routine correspondence. Responds promptly and professionally to customer needs. Gathers and analyzes information skillfully.
- Must be able to stand a minimum of eight hours and continuously lift, push, and pull. Requires the ability to stand for the majority of the shift in a cold working condition and the use of Personal Protective Equipment (i.e. safety equipment) such as hard hats, hair/beard nets, earplugs, etc.
Receipt & Acknowledgement: Signature: ____________________________________ Date: _____________________
Important Notice: This job description is a generalized summary of job duties and can be modified as determined as necessary by Colorado Premium. It is not a contract of employment. All employment is “at-will” an Employee or the Company may terminate employment at any time, with or without cause, and without advance notice, procedure, or formality.
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Associate Director Clinical Quality Assurance Job Market in Colorado
A snapshot from current Colorado openings, updated as new roles post.
Who's Hiring


Top Industries Hiring
- Manufacturing
- Technology & Software
- Consulting & Professional Services
- Electronics & Hardware
- Construction & Real Estate
What Colorado Employers Look For
The qualifications that appear most often in associate director clinical quality assurance jobs across Colorado.
- Bachelor's degree in life sciences, pharmacy, or a related field required
- Minimum seven years of clinical quality assurance experience in pharmaceutical or CRO settings
- Deep working knowledge of GCP, ICH guidelines, and FDA regulations
- Demonstrated experience leading internal and external GCP audits
- Prior people management experience overseeing quality assurance teams or direct reports
- Strong familiarity with CAPA processes, deviation management, and quality system documentation
Associate Director Clinical Quality Assurance Jobs in Colorado: Frequently Asked Questions
How do you become a associate director clinical quality assurance in Colorado?
Most associate director clinical quality assurance roles in Colorado require a bachelor's degree in a life sciences field and several years of progressive QA experience within clinical research, pharmaceutical development, or a contract research organization. Colorado does not issue a state-specific license for this role, but employers along the Front Range strongly favor candidates with certifications such as the Certified Quality Auditor credential from ASQ, which has an active Denver section. Advancing from senior QA specialist or QA manager positions at Colorado-based CROs or biopharma companies is the most common path.
Which companies hire associate director clinical quality assurances in Colorado?
Colorado associate director clinical quality assurance roles are posted by Sierra Space, Claremont Foods, and McLane Global and others right now, based on current listings on Migrate Mate as of July 2026. Colorado's concentration of CROs, specialty pharma companies, and large health systems in the Denver metro and Boulder areas makes it one of the more active markets in the region for this level of quality leadership.
Which Colorado cities have the most associate director clinical quality assurance jobs?
Denver, Louisville, and Westminster account for the largest share of associate director clinical quality assurance openings in Colorado. Denver and its southern suburbs drive the bulk of demand because that is where the state's largest health systems, CROs, and pharmaceutical operations are headquartered, while Boulder's biotech corridor and Fort Collins' growing life sciences sector generate consistent additional openings at this seniority level.
Are there remote associate director clinical quality assurance jobs in Colorado?
Yes, and more than you might expect for a compliance-focused leadership role, since much of the work involves document review, audit planning, and cross-functional oversight that can be done off-site. About 52% of associate director clinical quality assurance openings tied to Colorado are remote or hybrid as of July 2026, reflecting how CROs and global pharma sponsors have normalized distributed quality teams. The most fully remote positions tend to be in sponsor oversight and quality system management rather than hands-on clinical site auditing.
How can I get hired as a associate director clinical quality assurance in Colorado with little or no experience?
The most realistic entry path is through a quality assurance coordinator or clinical QA associate role at one of Colorado's active CROs or mid-size biopharma companies in the Denver or Boulder area, where internal promotion into management tracks is common. Companies such as large health systems and regional CROs running clinical trials often hire entry-level QA professionals and develop them through structured mentorship. Earning the ASQ Certified Quality Auditor credential early, building hands-on experience with GCP inspections, and moving laterally from clinical operations or regulatory affairs are the moves that open doors to director-track roles.
Where can I find and apply to associate director clinical quality assurance jobs in Colorado?
You can find and apply to associate director clinical quality assurance jobs in Colorado on Migrate Mate, which lists current openings from employers across the state. Search the available roles, find the ones that fit your background and location, and apply directly to the ones that match.
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