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Laboratory Manager, Product Development QA

Job in North Chicago, Lake County, Illinois, 60086, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-09-21
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist - Analyst/Manager, Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers, Data Analyst
Salary/Wage Range or Industry Benchmark: 125000 - 170000 USD Yearly USD 125000.00 170000.00 YEAR
Job Description & How to Apply Below

Purpose

Primarily responsible for leading Product Development QA from an analytical perspective in support of clinical supply release.

Responsibilities
  • Support CMC teams in resolving complex technical Analytical challenges through various phases of development
  • Provide leadership and daily support to the Lab QA team
  • Drive continuous process improvement within Product Development QA by updating/authoring policies, processes, procedures, and related documents
  • Lead QA Analytical audit/inspection preparation activities and support audits/inspections as the QA SME
  • Develop, maintain, and report key quality metrics to Management
  • Lead for analytical testing batch release; coordinate and resolve issues
  • Review and approve excipient, drug substance, and product specifications, including justification and revisions
  • Write/review/approve exception reports, including high impact and complex ERs impacting multifunctional areas
  • Approve Laboratory investigations
  • Assess compliance to regulations and industry practice and implement applicable process changes
Qualifications
  • Bachelor’s degree or equivalent experience required (typically life sciences or engineering);
    Master’s preferred
  • 6–8 years of experience in a related field, preferably with quality assurance and/or analytical sciences
  • Strong understanding of Active Pharmaceutical Ingredients (API) and drug product GMP manufacturing as applied to laboratory operations
  • Strong understanding of Quality Assurance principles and systems
  • Strong understanding of US and international regulations for quality systems and compliance for investigational products
  • Experience in project management, coordination, and planning of complex activities
  • Collaborative, risk-based approach to problem solving
  • Effective oral and written communication to clearly communicate quality position and actions needed to resolve issues
  • Ability to present and justify quality requirements across all levels of management
Benefits (as stated)
  • Paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k) to eligible employees
  • Eligible to participate in long-term incentive programs
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