Quality Assurance Technician

Hours for this role are 7:00am-3:30pm, M-F

Job DescriptionInspects shipments, reconciles labels, reviews and releases finished product and other paperwork.Reviews and approves/rejects other various quality-related documents.Assists in planning, developing, and implementing quality assurance programs.Responds to customer requests, including but not limited to investigating complaints and completing required paperwork for corrective and preventive actions and associated follow-up.Assists in changing and maintaining ISO and cGMP paperwork. Trains or oversees training.Ensures the quality requirements of all departments are being followed and are accurately documented.Interprets, understands, and manages a variety of technical information.Prepares routine, technical and special presentations/reports to staff and management as required.Prepares and compiles statistical analysis of quality assurance data.Oversees the writing and maintaining of owner’s process manuals.May coordinate and perform quality assurance system internal audits, investigate non-conformances and determine root cause analyses.Reviews the current policies determining and documenting any areas that may need quality improvements.This role is in the lab but not doing benchtop testing. You will be in front of a computer most of the day.Will compile lab results.Will ensure lab results are within specifications.Will ensure testing, materials, and results are within compliance.Will work with the QC department as well as the pilot plant.Perform other duties as assigned.

Job Type

This is a Contract-to-Hire position with a duration of 6 Month(s).

Work Site

This is a fully on-site position in Aurora, Ohio.

Work Environment

Fast paced work environment. Super clean warehouse environment as they are FDA regulated. They are big on teamwork and culture. Our 65,000 sq. ft. manufacturing facility in Aurora, OH, USA includes a 12,000 sq. ft. excipient processing center, 3,000 sq. ft. for repackaging, 35,000 sq. ft. warehouse, 8,000 sq. ft. office, 8,000 sq. ft. manufacturing area, and 1,000 sq. ft. quality control and R&D laboratory. You will work on the manufacturing floor sometimes to conduct tests, with the majority of the time being in front of a computer.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.