Sr. Quality Assurance Specialist

Job ***** Sr. QA Specialist** Cincinnati, OH (Hybrid)Contract * 6-12 MonthsPay * Commensurate with experience Ready to make a real impact in pharmaceutical quality operations?Kelly Scientific is looking for an experienced Sr.QA Specialist to resolve deviation investigations in a regulated pharma manufacturing environment. This is an exciting 6-month minimum (likely 1 year) contract opportunity with a leading pharmaceutical company, offering full benefits and the chance to apply your analytical skills to meaningful quality work.What You'll *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.) *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 **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.Why You Should ***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.Apply today and help shape the future of pharmaceutical quality assurance.Kelly Scientific is proud to be an Equal Opportunity Employer.

Created: 2025-05-22