Quality Assurance Coordinator

Quality Assurance Coordinator Kelly® Science & Clinical is seeking a for  Quality Assurance Coordinator a contract position at a cutting-edge consumer product in, Lititz, PA.   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.

Pay Rate: $27-$28.40 /hr depending on experience Schedule: M-F First Shift on site Length of assignment: one-year possible extension Bring your own IT device laptop role The Contract QA Specialist will provide support to business partners by monitoring process/status of investigations and CAPAs for products made at the Lititz site. As the Contract QA Specialist for the Lititz INV/CAPA process, the specialist will be responsible for monitoring data for the investigation results, ensuring timelines are met, updating and monitoring Investigation Track and Trends.

This role is responsible for administration, effectiveness and continuous monitoring of the INV and CAPA process along with providing metrics for INVs/CAPAs. Are you interested in joining a diverse team influencing strategy and delivering outstanding results to our customers? Apply now for this exciting opportunity! Key Responsibilities: 	 Monitor  INV/CAPA process and assist in monitoring site investigations and ensure appropriate resources are assigned and responsibilities are clearly outlined with due dates.

Provide Metrics for INVs/CAPAs. 	 Track and Trend investigations and CAPA as required. Support CAPA Review Board and lead as required. 	 Support investigation and CAPA partners by monitoring due datSupport Customer Complaints by investigating complaints and providing summary of findings. 	 Provide detailed or summary communication to QA management on status of key initiatives and issues related to investigation and CAPA due dates.

	 Perform and understand investigation trending in order to determine appropriate INV or CAPA trend responses, and ensure metrics are readily available for reporting. Use metrics to ensure all investigations are drafted to meet specified timelines and are completed prior to the release of associated product(s). 	 Establish relationships with Operation’s business partners by understanding their need, developing a trusting environment.

Additionally, Interact with various management levels and other business partners responsible for investigations and CAPAs to facilitate timely INV/CAPA closures. Education: 	 High School Diploma Experience: 	 Basic knowledge (Plant QA experience preferred) in either Pharmaceutical, Medical Device, OTC Drug, Cosmetic and/or Food and Dietary Supplements Production 	 Knowledge, Skills and Abilities: 	 Ability to collaborate with internal/external partners to enhance relationships and interactions, including interaction with management to inform, inspire change, and provide direct feedback.

	 Proven track record to accomplish work goals, with a modest amount of daily direction and oversight. 	 Ability to be on site daily 	 Quality Process and Systems Experience, especially with SOPs, MWI, Change Controls, Non-Conformance Investigation Documentation 	 Problem Solving   What happens next:   Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit.

But don’t worry – even if this position doesn’t work out, you’re still in our network and we can help find something that may be a better fit for you! That also means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless. #P1   10371125