QA Specialist

Company : Kelly Services
Location : West Chester, OH, 45069-1860
Posted Date : 3 October 2025
Job Details
Kelly Outsourcing Consulting Group Kelly OCG, a managed solution provider and business unit of Kelly Services, Inc., is currently seeking a **SR QA Specialist** for a year-long engagement at one of our Global client in **West Chester, OH** . This role is a full-time, fully benefited position. As a Kelly OCG employee you will be eligible for Medical, Dental, 401K, and a variety of other benefits to choose from. You'll also be eligible for paid time off, including holiday, vacation, and sick/personal time. All Kelly OCG employees receive annual performance review.
- *Job Title:** Sr. QA Specialist
- *Location:** West Chester, OH (Hybrid schedule)
- *Contract Length:** 6-12 Months
- *Pay Rate:** Commensurate with experience
- *What You'll Do:**
- Lead detailed investigations into manufacturing deviations with a focus on non-critical issues.
- Develop and execute investigation strategies with clear timelines and defined scopes.
- Author comprehensive investigation reports, including issue definition, root cause analysis, and CAPA (Corrective and Preventive Action) recommendations.
- Collaborate with cross-functional teams (Quality, Manufacturing, Engineering, etc.) to:
- Establish communication and investigation strategies.
- Define problem statements and identify root causes.
- Recommend and document effective CAPAs and follow-up actions.
- Leverage internal and external subject matter expertise to strengthen investigation quality.
- Ensure timely documentation and escalation of findings as needed.
- Manage multiple investigations simultaneously in a fast-paced, compliance-driven environment.
- *What You Bring:**
- *Required:**
- Strong ability to quickly interpret technical data and perform structured investigations.
- Clear, concise communication and exceptional technical writing skills.
- Accountability and follow-through from start to finish of the investigation process.
- Comfortable in a fast-paced, changing environment.
- Proficiency with Microsoft Office; working knowledge of QMS platforms like Veeva is a plus.
- Background in Pharmaceutical Manufacturing or other FDA-regulated industries.
- Familiarity with cGMP guidelines and quality systems.
- Experience using problem-solving methodologies (e.g., Fishbone, 5 Whys).
- Bachelor's degree in a Science, Engineering, or related technical field.
- Previous experience in Quality Deviation or CAPA management.
- Get your foot in the door with a top pharmaceutical organization.
- Gain valuable experience leading quality investigations that ensure product safety and regulatory compliance.
- Enjoy full benefits while working on a short-term contract with long-term impact.
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