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Director Control Testing Jobs (NOW HIRING)

Perform standard quality control testing on incoming raw materials, semi-finished goods, and ... Complete and control the required quality records and/or documents as directed by the department ...

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$125.6K

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How much do director control testing jobs pay per year?

As of Sep 10, 2026, the average yearly pay for director control testing in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Director Control Testing job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 20% Part Time, 3% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Executive Director & Site Quality Lead

Salt Lake City, UT โ€ข On-site

Scorpion Therapeutics
51 - 200 employees

Other

Medical, Retirement

Posted 11 days ago


Job description

Key Accountabilities/Core Job Responsibilities
  • Oversee GMP/GLP Quality operations in Utah, including QC labs/testing, batch record reviews and release, environmental monitoring, and external testing labs.
  • Ensure overall site compliance and inspection readiness for health authority inspections.
  • Partner with the Utah site head on site culture, longโ€‘term strategy, and inspection readiness.
  • Build, supervise, develop, promote, hire, and train the GxP QA/QC team.
  • Represent Quality on the Utah Site Leadership Team and Denali Quality Leadership Team.
  • Establish and monitor site quality metrics/KPIs for performance monitoring and Quality System Management Reviews.
  • Implement/maintain/optimize quality systems (document control, change management, deviations, CAPAs, audits, compliance initiatives).
  • Support GMP site qualification (SOPs, work instructions, specifications, stability studies, method validations, test methods, utility/equipment/room qualifications).
  • Lead direct reports (goal setting, growth planning, training compliance, feedback).
Qualifications/Skills
  • BS in a scientific discipline (MS and quality/compliance/regulatory certification preferred); 15+ years GMP pharmaceutical experience, including 12+ years people leadership.
  • Experience with in-house manufacturing, QC testing, and CMC development.
  • Large molecule/commercialization experience (plus).
  • Inspection management, mock inspections, Health Authority interactions.
  • Strong knowledge of 21 CFR 210-211, Part 11, 610 & 820; EU cGMP/GLPs; ICH quality/guidelines.
  • Familiarity with eQMS systems.
  • Domestic and international travel.
Benefits
  • Competitive total rewards package including 401k, healthcare coverage, and ESPP.
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