Director of Quality
Location: Sanford, FL
Ready to take the next step into leadership? This is a unique opportunity to step into a Director-level role where you’ll shape and elevate the Quality function at a growing, agile organization. You’ll have the autonomy to influence systems, drive compliance strategy, and make a lasting impact on product quality and patient outcomes.
Why You Should Apply
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Competitive salary range
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Ideal “step-up” Director role with high visibility and ownership
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Opportunity to build, refine, and lead quality systems in a growing company
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Direct influence on compliance strategy and regulatory readiness
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Collaborative leadership environment with executive exposure
What You’ll Be Doing
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Lead and oversee core Quality Systems including deviations, CAPA, change control, and audits
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Guide quality strategy to ensure compliance with cGMP and regulatory standards
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Review and approve critical QA documentation including batch records and SOPs
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Drive continuous improvement initiatives across QA/QC functions
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Partner cross-functionally with operations, manufacturing, and leadership teams
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Prepare for and support regulatory inspections and internal audits
About You
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Bachelor’s degree in a scientific discipline (Chemistry, Biology, Pharmacy, or related)
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Strong expertise in cGMP and pharmaceutical quality systems
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Experience leading or owning quality programs and compliance initiatives
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Proficiency with eQMS and quality documentation systems
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Strategic thinker with strong communication and leadership presence
How To Apply
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to
emily@scientificsearch.com and tell me why you’re interested. Or, feel free to email your resume. Please include Job#19808.