Associate Director Clinical Quality Assurance Jobs in Miami, FL
Associate Director Clinical Quality Assurance jobs in Miami are concentrated in Brickell, Doral, and the Wynwood-Midtown biotech corridor, with strong demand across pharmaceuticals, medical devices, and clinical research organizations. Employers hiring right now include Sofie, Lennar, and DO &. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 14+ Associate Director Clinical Quality Assurance jobs
- 401(k)
- 401(k) matching
- Paid time off
Department: Quality Assurance / Research & Development
Employment Type: Full-Time
- Develop, optimize, and evaluate cosmetic formulations based on customer needs, internal projects, and new raw materials.
- Design and conduct laboratory trials, formulation screening, compatibility studies, and stability evaluations.
- Maintain detailed laboratory notebooks and technical development records in accordance with Good Documentation Practices (GDP).
- Analyze experimental results, troubleshoot formulation challenges, and propose creative, science-based solutions.
- Research new ingredients, technologies, and market trends to support product innovation.
- Maintain the R&D laboratory in a clean, organized, and inspection-ready condition.
- Manage laboratory inventory, chemicals, reference materials, and consumables.
- Perform equipment verification, internal calibrations, and routine maintenance according to SOPs.
- Ensure compliance with laboratory safety procedures, GMP requirements, and good laboratory practices.
- Perform quality control testing of raw materials, finished products, and development batches when required.
- Issue Certificates of Analysis (COAs) following completion and review of laboratory testing.
- Maintain retain samples and development sample inventory.
- Support laboratory investigations, retests, stability programs, and analytical evaluations.
- Maintain complete, accurate, and organized laboratory records in accordance with GMP and GDP requirements.
- Provide technical support to Sales and customers regarding formulation, product performance, and ingredient applications.
- Prepare technical reports, formulation guidelines, and laboratory summaries.
- Support new product implementation, technical documentation, and change control activities.
- Collaborate with suppliers to evaluate new technologies and resolve technical questions.
- Collaborate with the Quality Control, Regulatory, and Production teams to support business priorities.
- Assist with incoming material inspections, Quality Checks, and laboratory investigations as needed.
- Provide technical support during manufacturing, scale-up activities, and process troubleshooting.
- Participate in continuous improvement initiatives, SOP development, GMP compliance activities, and internal audits.
- Scientific curiosity and creativity.
- Strong analytical and problem-solving skills.
- Excellent organization and attention to detail.
- A proactive attitude and willingness to take ownership of laboratory operations.
- Adaptability and enthusiasm for learning new skills.
- The ability to balance multiple priorities in a dynamic environment.
- A collaborative mindset and willingness to support other Quality Department activities as business needs evolve.
- 401(k)
- 401(k) matching
- Paid time off
Department: Quality Assurance / Research & Development
Employment Type: Full-Time
- Develop, optimize, and evaluate cosmetic formulations based on customer needs, internal projects, and new raw materials.
- Design and conduct laboratory trials, formulation screening, compatibility studies, and stability evaluations.
- Maintain detailed laboratory notebooks and technical development records in accordance with Good Documentation Practices (GDP).
- Analyze experimental results, troubleshoot formulation challenges, and propose creative, science-based solutions.
- Research new ingredients, technologies, and market trends to support product innovation.
- Maintain the R&D laboratory in a clean, organized, and inspection-ready condition.
- Manage laboratory inventory, chemicals, reference materials, and consumables.
- Perform equipment verification, internal calibrations, and routine maintenance according to SOPs.
- Ensure compliance with laboratory safety procedures, GMP requirements, and good laboratory practices.
- Perform quality control testing of raw materials, finished products, and development batches when required.
- Issue Certificates of Analysis (COAs) following completion and review of laboratory testing.
- Maintain retain samples and development sample inventory.
- Support laboratory investigations, retests, stability programs, and analytical evaluations.
- Maintain complete, accurate, and organized laboratory records in accordance with GMP and GDP requirements.
- Provide technical support to Sales and customers regarding formulation, product performance, and ingredient applications.
- Prepare technical reports, formulation guidelines, and laboratory summaries.
- Support new product implementation, technical documentation, and change control activities.
- Collaborate with suppliers to evaluate new technologies and resolve technical questions.
- Collaborate with the Quality Control, Regulatory, and Production teams to support business priorities.
- Assist with incoming material inspections, Quality Checks, and laboratory investigations as needed.
- Provide technical support during manufacturing, scale-up activities, and process troubleshooting.
- Participate in continuous improvement initiatives, SOP development, GMP compliance activities, and internal audits.
- Scientific curiosity and creativity.
- Strong analytical and problem-solving skills.
- Excellent organization and attention to detail.
- A proactive attitude and willingness to take ownership of laboratory operations.
- Adaptability and enthusiasm for learning new skills.
- The ability to balance multiple priorities in a dynamic environment.
- A collaborative mindset and willingness to support other Quality Department activities as business needs evolve.
See All 14 Associate Director Clinical Quality Assurance Jobs in Miami
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Find JobsAssociate Director Clinical Quality Assurance Job Market in Miami
Who's Hiring
Top Industries Hiring
- Insurance
- Aerospace & Defense
- Healthcare & Medical Services
Associate Director Clinical Quality Assurance Jobs in Miami: Frequently Asked Questions
How do I get a associate director clinical quality assurance job in Miami?
Miami's strongest hiring comes from pharmaceutical companies and contract research organizations clustered in Doral and Brickell, along with the growing med-tech sector near the Health District. Candidates with experience in FDA regulatory frameworks, GCP auditing, or clinical trial oversight stand out locally. Networking through the South Florida chapter of the Regulatory Affairs Professionals Society and targeting CROs that run Latin American clinical programs gives Miami applicants a concrete edge.
Which companies hire associate director clinical quality assurances in Miami?
Employers hiring associate director clinical quality assurances in Miami right now include Sofie, Lennar, and DO &, based on current listings on Migrate Mate as of July 2026. Miami's mix of global pharma subsidiaries, locally headquartered CROs, and hospital-affiliated research centers makes it a varied market for this role.
Are there remote associate director clinical quality assurance jobs in Miami?
Yes, though with limits, since associate director clinical quality assurance work involves audits, site visits, and direct oversight that often require in-person presence. About 40% of associate director clinical quality assurance openings tied to Miami are remote or hybrid as of July 2026, with flexibility most common for quality systems management and SOP development roles rather than hands-on clinical site oversight.
How can I get a associate director clinical quality assurance job in Miami with little or no experience?
The most realistic path in Miami is moving up through quality assurance specialist or senior QA associate roles at a local CRO or pharmaceutical company in Doral or the Health District, where internal promotion to director-track positions is common. Entry-level QA analysts at Miami's hospital research networks and biotech startups in Wynwood often gain the GCP and regulatory audit exposure needed to make the jump within three to five years.
Which industries hire the most associate director clinical quality assurances in Miami?
The sectors hiring the most associate director clinical quality assurances in Miami are Insurance, Aerospace & Defense, and Healthcare & Medical Services, based on current listings on Migrate Mate as of July 2026. Miami's role as a regional hub for Latin American clinical trials and its concentration of pharma distribution and medical device firms drives consistent demand across these sectors.
See All 14 Associate Director Clinical Quality Assurance Jobs in Miami
Find roles in Miami that match your experience and apply in just a few clicks.
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