Associate Director Clinical Quality Assurance Jobs in New Mexico
Associate Director Clinical Quality Assurance jobs in New Mexico are concentrated in the pharmaceutical, biotech, and clinical research sectors, with consistent demand at the senior individual contributor and people-management levels. Most hiring activity centers on Albuquerque, Santa Fe, and Rio Rancho, where established employers such as Presbyterian Healthcare Services, Lovelace Health System, and Sandia National Laboratories maintain ongoing quality and compliance functions. The most in-demand specialties include GCP auditing, regulatory submissions support, and clinical trial quality oversight. See the openings below and apply to the ones that match your experience.
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Showing 5 of 13+ Associate Director Clinical Quality Assurance jobs
Work Location: On-Site at WIPP
The Waste Isolation Pilot Plant (WIPP) is the nation’s only permanent nuclear waste repository for defense-generated transuranic (TRU) waste generated from Department of Energy (DOE) sites across the country. Waste is permanently isolated over 2,000 feet underground in deep salt beds.
Position Overview:
Duties:
- Perform supplier audits, surveillances, and quality assessments.
- Support implementation and maintenance of NQA-1 compliant programs.
- Review technical, quality, and turnover documentation.
- Provide oversight of fabrication, installation, inspection, and testing activities.
- Evaluate supplier corrective actions and quality performance trends.
- Support startup, commissioning, and system turnover activities.
- Coordinate with engineering, construction, testing, procurement, and project management organizations.
- Ensure compliance with applicable regulatory, contractual, and industry requirements.
- Promote a strong nuclear safety culture and continuous improvement environment.
Nuclear Quality Assurance
- Extensive knowledge of NQA-1 Quality Assurance requirements.
- Working knowledge of 10 CFR 50 Appendix B and 10 CFR 21.
- Experience developing, implementing, and maintaining nuclear QA programs.
- Ability to perform quality program assessments, audits, surveillances, and inspections.
- Experience supporting regulatory and utility audits.
- Strong understanding of corrective action programs and root cause evaluation.
- Experience managing supplier quality assurance programs.
- Conducting supplier audits, annual evaluations, and surveillance activities.
- Evaluated Supplier List (ESL) management and supplier qualification.
- Commercial Grade Dedication (CGD) program knowledge.
- Supplier document reviews and compliance verification.
- Ability to interface with supplier management and resolve quality issues.
- Working knowledge of ASME Section III and Section XI requirements.
- Experience with system turnover, testing boundaries, and hold point establishment.
- Knowledge of AWS welding requirements and quality controls.
- Understanding of material traceability, CMTRs, MTRs, CoCs, and turnover documentation.
- ASNT VT Level II certification preferred.
- Experience performing weld inspections and NDE surveillance.
- Fabrication shop and field construction oversight experience.
- Mechanical and structural component inspection experience.
- Receipt inspection and acceptance testing support.
- Ability to evaluate nonconformances and support disposition activities.
- Strong verbal and written communication skills.
- Experience coordinating cross-functional teams.
- Proven ability to develop procedures, training programs, and process improvements.
- Ability to mentor personnel and support organizational development.
- Experience presenting technical information to senior management and project stakeholders.
- Bachelor’s Degree in Engineering, Industrial Leadership, Construction Management,
- or related field.
- NQA-1 Lead Auditor qualification.
- ASNT VT Level II Certification.
- Experience supporting DOE and Commercial Nuclear projects.
- Experience with AP1000, SSC turnover, startup testing, commissioning, or nuclear construction projects.
- Experience serving as a Subject Matter Expert (SME) for supplier quality, audits, or quality program implementation.
- United States Citizenship
- Active DOE “Q” Clearance
WORKING WITH EDGEWATER
Edgewater is committed to recruiting and maintaining a staff of highly skilled professionals to support our customers. In keeping with this objective, we offer highly competitive salaries and employee benefit packages structured to best suit your needs. We offer multiple individual and family benefit options including paid time off, medical, dental, life, vision, and disability insurance, and a pre-tax 401 (k) retirement account with Company matching contributions and 100% vesting for eligible participants beginning DAY 1.
EQUAL OPPORTUNITY EMPLOYER
View all Edgewater opportunities at www.edgewatertech.net/careers
Work Location: On-Site at WIPP
The Waste Isolation Pilot Plant (WIPP) is the nation’s only permanent nuclear waste repository for defense-generated transuranic (TRU) waste generated from Department of Energy (DOE) sites across the country. Waste is permanently isolated over 2,000 feet underground in deep salt beds.
Position Overview:
Duties:
- Perform supplier audits, surveillances, and quality assessments.
- Support implementation and maintenance of NQA-1 compliant programs.
- Review technical, quality, and turnover documentation.
- Provide oversight of fabrication, installation, inspection, and testing activities.
- Evaluate supplier corrective actions and quality performance trends.
- Support startup, commissioning, and system turnover activities.
- Coordinate with engineering, construction, testing, procurement, and project management organizations.
- Ensure compliance with applicable regulatory, contractual, and industry requirements.
- Promote a strong nuclear safety culture and continuous improvement environment.
Nuclear Quality Assurance
- Extensive knowledge of NQA-1 Quality Assurance requirements.
- Working knowledge of 10 CFR 50 Appendix B and 10 CFR 21.
- Experience developing, implementing, and maintaining nuclear QA programs.
- Ability to perform quality program assessments, audits, surveillances, and inspections.
- Experience supporting regulatory and utility audits.
- Strong understanding of corrective action programs and root cause evaluation.
- Experience managing supplier quality assurance programs.
- Conducting supplier audits, annual evaluations, and surveillance activities.
- Evaluated Supplier List (ESL) management and supplier qualification.
- Commercial Grade Dedication (CGD) program knowledge.
- Supplier document reviews and compliance verification.
- Ability to interface with supplier management and resolve quality issues.
- Working knowledge of ASME Section III and Section XI requirements.
- Experience with system turnover, testing boundaries, and hold point establishment.
- Knowledge of AWS welding requirements and quality controls.
- Understanding of material traceability, CMTRs, MTRs, CoCs, and turnover documentation.
- ASNT VT Level II certification preferred.
- Experience performing weld inspections and NDE surveillance.
- Fabrication shop and field construction oversight experience.
- Mechanical and structural component inspection experience.
- Receipt inspection and acceptance testing support.
- Ability to evaluate nonconformances and support disposition activities.
- Strong verbal and written communication skills.
- Experience coordinating cross-functional teams.
- Proven ability to develop procedures, training programs, and process improvements.
- Ability to mentor personnel and support organizational development.
- Experience presenting technical information to senior management and project stakeholders.
- Bachelor’s Degree in Engineering, Industrial Leadership, Construction Management,
- or related field.
- NQA-1 Lead Auditor qualification.
- ASNT VT Level II Certification.
- Experience supporting DOE and Commercial Nuclear projects.
- Experience with AP1000, SSC turnover, startup testing, commissioning, or nuclear construction projects.
- Experience serving as a Subject Matter Expert (SME) for supplier quality, audits, or quality program implementation.
- United States Citizenship
- Active DOE “Q” Clearance
WORKING WITH EDGEWATER
Edgewater is committed to recruiting and maintaining a staff of highly skilled professionals to support our customers. In keeping with this objective, we offer highly competitive salaries and employee benefit packages structured to best suit your needs. We offer multiple individual and family benefit options including paid time off, medical, dental, life, vision, and disability insurance, and a pre-tax 401 (k) retirement account with Company matching contributions and 100% vesting for eligible participants beginning DAY 1.
EQUAL OPPORTUNITY EMPLOYER
View all Edgewater opportunities at www.edgewatertech.net/careers
See All 13 Associate Director Clinical Quality Assurance Jobs in New Mexico
Find roles in New Mexico that match your experience and apply in just a few clicks.
Find JobsAssociate Director Clinical Quality Assurance Jobs by City in New Mexico
Where New Mexico roles are concentrated, by current openings.
Associate Director Clinical Quality Assurance Job Market in New Mexico
A snapshot from current New Mexico openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Government & Public Sector
- Technology & Software
- Biotechnology & Pharmaceuticals
What New Mexico Employers Look For
The qualifications that appear most often in associate director clinical quality assurance jobs across New Mexico.
- Bachelor's or advanced degree in life sciences, nursing, pharmacy, or a related field required
- Minimum seven years of clinical quality assurance experience in pharmaceutical or healthcare settings
- Deep working knowledge of FDA regulations, ICH guidelines, and GCP standards
- Proven experience leading QA audits, CAPA programs, and inspection readiness activities
- Prior people management experience overseeing QA teams or cross-functional compliance groups
- Familiarity with electronic quality management systems such as Veeva Vault or MasterControl
Associate Director Clinical Quality Assurance Jobs in New Mexico: Frequently Asked Questions
How do you become a associate director clinical quality assurance in New Mexico?
Most associate director clinical quality assurance roles in New Mexico require a bachelor's degree in a life science, nursing, or pharmacy discipline, followed by progressive QA experience in clinical research or healthcare. New Mexico does not issue a state-specific license for this role, but employers routinely expect certifications such as Certified Quality Auditor through ASQ or RAC through RAPS. Candidates who gain experience at New Mexico's hospital systems or national labs typically move into director-level QA positions from senior specialist or QA manager roles.
Which companies hire associate director clinical quality assurances in New Mexico?
Companies currently hiring associate director clinical quality assurances in New Mexico include State of New Mexico, Curia, and Los Alamos National Laboratory, per current listings on Migrate Mate as of July 2026. New Mexico's concentration of federally funded research institutions and regional health systems means demand is relatively steady regardless of broader hiring cycles.
Which New Mexico cities have the most associate director clinical quality assurance jobs?
The cities with the most associate director clinical quality assurance openings in New Mexico are Albuquerque, Las Cruces, and Los Alamos. Albuquerque drives the majority of listings as the state's largest metro, home to its major hospital networks and proximity to federally affiliated research operations, while Santa Fe and Rio Rancho contribute openings tied to state-level health agencies and expanding biotech and medical device employers in the metro corridor.
Are there remote associate director clinical quality assurance jobs in New Mexico?
Yes, and more than many clinical roles, since associate director clinical quality assurance work is heavily documentation-driven and can be performed off-site when not conducting on-site audits. About 0% of associate director clinical quality assurance openings tied to New Mexico are remote or hybrid as of July 2026, reflecting growing acceptance of distributed QA leadership. Document review, SOP authoring, and CAPA management are the functions most frequently performed remotely.
How can I get hired as a associate director clinical quality assurance in New Mexico with little or no experience?
The most realistic entry path is through a quality or clinical research coordinator role at one of New Mexico's health systems, such as Presbyterian Healthcare Services or UNM Health, where exposure to GCP documentation and audit support builds the foundation employers expect. From there, lateral moves into QA specialist or clinical trial associate positions open the door to director-track progression. Earning an ASQ Certified Quality Auditor credential or completing a clinical research certificate program through the University of New Mexico strengthens a candidate's profile considerably before applying to associate director openings.
Where can I find and apply to associate director clinical quality assurance jobs in New Mexico?
You can find and apply to associate director clinical quality assurance jobs in New Mexico on Migrate Mate, which lists current openings across the state. Search the listings, identify the roles that fit your background and experience level, and apply directly to the ones that match.
See All 13 Associate Director Clinical Quality Assurance Jobs in New Mexico
Find roles in New Mexico that match your experience and apply in just a few clicks.
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