Quality Assurance Director
Scientific Search, Sanford, FL, United States
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
Competitive salary range
Ideal “step-up” Director role with high visibility and ownership
Opportunity to build, refine, and lead quality systems in a growing company
Direct influence on compliance strategy and regulatory readiness
Collaborative leadership environment with executive exposure
What You’ll Be Doing
Lead and oversee core Quality Systems including deviations, CAPA, change control, and audits
Guide quality strategy to ensure compliance with cGMP and regulatory standards
Review and approve critical QA documentation including batch records and SOPs
Drive continuous improvement initiatives across QA/QC functions
Partner cross-functionally with operations, manufacturing, and leadership teams
Prepare for and support regulatory inspections and internal audits
About You
Bachelor’s degree in a scientific discipline (Chemistry, Biology, Pharmacy, or related)
Strong expertise in cGMP and pharmaceutical quality systems
Experience leading or owning quality programs and compliance initiativesProficiency with eQMS and quality documentation systems
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.
#J-18808-Ljbffr
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
Competitive salary range
Ideal “step-up” Director role with high visibility and ownership
Opportunity to build, refine, and lead quality systems in a growing company
Direct influence on compliance strategy and regulatory readiness
Collaborative leadership environment with executive exposure
What You’ll Be Doing
Lead and oversee core Quality Systems including deviations, CAPA, change control, and audits
Guide quality strategy to ensure compliance with cGMP and regulatory standards
Review and approve critical QA documentation including batch records and SOPs
Drive continuous improvement initiatives across QA/QC functions
Partner cross-functionally with operations, manufacturing, and leadership teams
Prepare for and support regulatory inspections and internal audits
About You
Bachelor’s degree in a scientific discipline (Chemistry, Biology, Pharmacy, or related)
Strong expertise in cGMP and pharmaceutical quality systems
Experience leading or owning quality programs and compliance initiativesProficiency with eQMS and quality documentation systems
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.
#J-18808-Ljbffr