More jobs:
Site Quality Head, R&D
Job in
Reading, Berks County, Pennsylvania, 19610, USA
Listed on 2026-07-10
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
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.
- 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).
- Familiarity with GLP, GCP, and GCLP; analytical method/equipment qualification knowledge.
- ASQ or ISO Certified Auditor; quality system certification training.
- Strong problem solving, report writing, and communication.
- High-quality healthcare, prevention and wellness programs, and at least 14 weeks' gender-neutral parental leave; mentoring and international mobility programs.
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×