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Site Quality Head, R&D

Job in Reading, Berks County, Pennsylvania, 19610, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-07-10
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers
Salary/Wage Range or Industry Benchmark: 120000 - 150000 USD Yearly USD 120000.00 150000.00 YEAR
Job Description & How to Apply Below

Main Responsibilities

  • Provide site leadership and direction for R&D quality and compliance systems for clinical testing laboratories and early-phase clinical trial material manufacturing/testing/release (internal and via CMO/CRO partners).
  • Direct 3-5 quality professionals to ensure effective GxP compliance; develop and maintain an Annual Quality Plan based on site performance metrics.
  • Represent Vaccines R&D Quality Swiftwater on the R&D Quality Leadership Team: set priorities, define improvement initiatives, and develop/manage budget; act as quality SME for local R&D.
  • Quality systems management: educate and guide on GLP/GCP/GMP; liaise with Quality Risk Manager for risk mapping/remediation; collaborate with global R&D Quality and local Manufacturing & Supply Quality.
  • Audits/inspections: lead readiness for internal/external/third-party audits; ensure quality oversight of third-party suppliers/subcontractors (incl. quality agreements); defend quality programs and respond to audit findings.
  • Continuous improvement/quality culture: support quality system improvements; report quality metrics; define annual evaluation programs; support corrective actions.
  • Community of Practice: implement standardized local processes/tools; act as "Voice of Customer"; share best practices and propose improvements.
  • Health, Safety & Compliance: oversee compliance with employment/health/safety legislation; respond to safety incidents and support investigations; complete required documentation.
Qualifications
  • BS in Biology/Microbiology/Biochemistry (or related) OR MSc/PhD in Immunology/Microbiology/Biochemistry (or related).
  • 10+ years relevant experience (preferably pharma/biotech), with substantial supervisory experience.
  • Excellent knowledge of GMPs (US, Canada, Europe).
Preferred
  • Familiarity with GLP, GCP, and GCLP; analytical method/equipment qualification knowledge.
  • ASQ or ISO Certified Auditor; quality system certification training.
Skills
  • Strong problem solving, report writing, and communication.
Benefits
  • High-quality healthcare, prevention and wellness programs, and at least 14 weeks' gender-neutral parental leave; mentoring and international mobility programs.
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