QA Associate II

Job Description

Job Description

Kelly® Science & Clinical is seeking a QA Associate II for a 2-year contract position with a national pharmaceutical leader at their site in West Chester, OH
. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Compensation: $30-32/hr

Schedule:

• Assignment 1 (August 2026-August 2027):
  Mon-Fri, 8AM-5:30PM
• Assignment 2 (August 2027-August 2028): 2/2/3, night shift

Location: West Chester, OH

This position is responsible for all QA activities that directly support execution of the process both within the Process Execution Team (PET) and in assigned areas outside of the PETs. These activities may include but are not limited to aseptic monitoring, on the floor review, batch record review, documentation support, forward processing, and walkthroughs.

• Processing classroom training documentation and granting credit within the eLMS. (learning management system)
• Reviewing/Verifying documents for training requirements in the eDMS (document management system) and creating training requirements as needed.
• Processing training assignments

At this level the incumbent is not necessarily performing all the essential job functions of the role immediately. The incumbent may begin by specializing in one or more of these responsibilities whilst working to develop a solid knowledge of the process being supported and applicable cGMPs. Over time the incumbent will be expected to obtain the necessary training to become skilled in all major responsibilities of the role.

• Maintain a high level of understanding of relevant production processes and quality systems
• Perform QA review of GMP documentation that has direct impact on the activities performed by and facilities utilized in their corresponding areas as applicable.
• Collaborate with and influences other Quality professionals across the organization to ensure consistent application and execution of key quality systems
• Execute QA processes including batch record review, forward processing, and quality issue resolution to maintain the flow of products and documents to meet site objectives
• Collaborate with and influence other PET/assigned area members to facilitate process improvements and risk assessments; benchmark QA practices to identify innovative efficient and effective practices
• Stay abreast of evolving regulatory compliance practices and recommend implementation strategies to area leaders

• High school diploma
• Considerable experience in Quality Assurance within a GMP setting
• Ability to become aseptic gowning certified and maintain certification
• Excellent oral and written communication skills
• Strong ability and motivation to learn

• Bachelor’s degree; master’s degree in quality assurance/regulatory affairs is desirable
• Previous experience in a Lean, process-centric organization with emphasis on continuous

improvement

• Multi-site / multi-functional experience

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources.

Kelly offers eligible employees voluntary benefit plans including

• medical
• dental
• vision
• telemedicine
• term life
• whole life
• accident insurance
• critical illness
• a legal plan
• and short-term disability

As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan.

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and c