Homeland

Supervisor II, Quality Assurance - Compliance & Oversight
Professional Services
Spokane, Washington Direct Hire Oct 22, 2026
Job Summary
Homeland Talent Solutions is partnering with an established pharmaceutical manufacturing organization in Spokane, Washington, to identify an experienced Supervisor II, Quality Assurance - Compliance & Oversight to join its Quality Assurance leadership team.

The Supervisor II, Quality Assurance will play a key role in maintaining regulatory compliance, product quality, and operational excellence within a highly regulated pharmaceutical manufacturing environment. This position offers the opportunity to provide hands-on Quality Assurance oversight of manufacturing operations while ensuring adherence to current Good Manufacturing Practices (cGMP).

The Supervisor II, Quality Assurance is an excellent opportunity for a quality professional with strong regulatory knowledge and proven experience, leading and developing QA personnel. If you enjoy solving complex compliance challenges, collaborating with manufacturing teams, and upholding the highest standards of product quality and patient safety, this role offers an opportunity to make a meaningful impact. 

Responsibilities
Quality Assurance & Manufacturing Oversight
  • Lead and supervise QA Compliance & Oversight personnel providing real-time quality oversight across manufacturing, packaging, warehouse, laboratory, and supporting operations
  • Ensure consistent execution of on-the-floor quality activities, including batch record reviews, process monitoring, area audits, and identification of potential compliance risks
  • Provide technical guidance and real-time support when quality events, manufacturing deviations, or operational concerns arise
  • Assess quality and compliance risks, determine appropriate escalation, and support timely resolution of manufacturing-related issues
  • Monitor compliance trends, recurring observations, and operational risks to identify opportunities for corrective action and process improvement
Team Leadership & Development
  • Oversee daily activities, staffing needs, performance expectations, and operational priorities for assigned QA personnel
  • Coach, mentor, and develop team members to strengthen technical capabilities, GMP knowledge, decision-making, and overall performance
  • Support recruitment, onboarding, training, performance management, and professional development initiatives
  • Promote a culture of accountability, collaboration, continuous improvement, and quality ownership
  • Ensure compliance with applicable FDA regulations, cGMP requirements, Good Documentation Practices (GDP), internal procedures, and established quality standards
Regulatory Compliance & Cross-Functional Collaboration
  • Collaborate with Manufacturing, Engineering, Validation, Quality Control, Packaging, and other operational teams to resolve quality issues and maintain compliance
  • Support regulatory inspections, client audits, internal audits, and ongoing inspection-readiness initiatives
  • Lead or participate in cross-functional investigations, corrective actions, and continuous improvement projects
  • Track and communicate departmental performance metrics related to quality oversight, compliance, audit readiness, and operational effectiveness

Requirements
  • Bachelor's degree in a scientific, technical, or related discipline
  • An associate degree with at least 7 years of directly related experience may be considered in lieu of a bachelor's degree
  • Minimum 4 years of relevant experience within pharmaceutical manufacturing or an FDA-regulated pharmaceutical environment
  • Previous supervisory or team leadership experience
  • Strong working knowledge of cGMP regulations, Good Documentation Practices, and pharmaceutical manufacturing operations
  • Direct experience providing or leading real-time, on-the-floor Quality Assurance oversight during manufacturing operations
  • Experience with batch record review, manufacturing process monitoring, area audits, quality event identification, and compliance risk assessment
  • Ability to evaluate deviations and quality concerns, assess potential product impact, and support appropriate escalation and resolution
  • Demonstrated ability to coach, mentor, and develop quality personnel
  • Strong communication, problem-solving, organizational, and cross-functional collaboration skills
  • Sound judgment and the ability to make timely, quality-focused decisions in an active manufacturing environment

Benefits
This role offers an annual salary of $84,975–$99,963, comprehensive benefits beginning on day one, and opportunities for annual compensation increases and career advancement. Benefits include medical, dental, and vision insurance, FSA and HSA options, life, and AD&D insurance, short- and long-term disability coverage, and an Employee Assistance Program (EAP). 

Summary
This is an excellent opportunity for an experienced pharmaceutical Quality Assurance professional to lead and develop a team while helping maintain the highest standards of product quality, regulatory compliance, and patient safety. Apply today! 

EEO Notice
Homeland LLC is an Equal Opportunity Employer. Homeland LLC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Homeland LLC complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. Reasonable accommodation is available for qualified individuals with disabilities, upon request.