Sr. Quality Assurance Specialist at Kelly Science, Engineering, Technology & Telecom

Acropolis Institute of Pharmaceutical Education and Research; Cincinnati (OH); Hybrid; USD 80,000 - 110,000; Full time

Job summary

A leading company in pharmaceutical quality operations is seeking a Sr. QA Specialist for a hybrid position in Cincinnati. This exciting contract role involves leading investigations into manufacturing deviations and collaborating with cross-functional teams to ensure quality and compliance. Applicants should possess strong technical writing skills and a background in pharmaceutical manufacturing.

Benefits

Full benefits

Short-term contract with long-term impact

Qualifications

• Strong ability to interpret technical data.
• Accountability and follow-through in investigations.
• Comfortable in a fast-paced, changing environment.

Responsibilities

• Lead investigations into manufacturing deviations.
• Develop investigation strategies and timelines.
• Author comprehensive investigation reports.

Skills

Technical writing

Problem-solving

Investigation

Communication

Analytical skills

Education

Bachelor’s degree in a Science, Engineering, or related technical field

Tools

Microsoft Office

QMS platforms like Veeva

Job description

Sr. Quality Assurance Specialist job at Kelly Science, Engineering, Technology & Telecom. Cincinnati, OH.

Job Title: Sr. QA Specialist

Location: Cincinnati, OH (Hybrid)

Contract Length: 6-12 Months

Pay Rate: 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 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.

Preferred:

• 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 Apply:

• 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.