Quality Control Associate

Job DescriptionThe primary focus of the Quality Control Associate I role will be to support drug product lot release and in-process testing within a cGMP environment.Perform or support cGMP lot release, in-process, and stability testing using various software packagesEnsure timely completion of testing and tasksSupport assay transfer and method validation of by executing cross-site validation protocols and providing data to support final reportsIdentify opportunities for continuous improvements.Maintain instrumentation and equipment preventative maintenance and supporting documentation in a cGMP compliant mannerAssist in the implementation of new assay methodologies and the associated instrumentation.Identify and support initiation of Deviations, CAPAs and Laboratory Investigations.Frequently required to stand; walk; sit; bend; stretch; use hands and fingers, with various manipulations; reach with hands and arms; and effectively communicate with others in the workplace, including the ability to make and promptly respond to audible cues and warnings.Work in areas that may have strong magnetsMay work in areas with exposure to vapor phase liquid nitrogen.Will be required to wear personal protective equipment (PPE) and other clean room garments daily. This may include, but not limited to: safety shoes, safety glasses, aprons, face shields, lab coats, full body gowns, hairnets, gloves, and hearing protection.Require to work in and around laboratories and controlled, enclosed, restricted areas, included clean rooms.Require to carry and/or lift up to 10 pounds several times a day.Lab w/ blood & animalPosition Handles Hazardous MaterialsQualificationsBS (Required) in Scientific discipline. Microbiology preferred.0-3 years of regulated industry experience, or equivalent combination of education and experience.Ability to work in a high paced team environment, meet deadlines, and prioritize work from multiple projects.Strong analytical and communication skillsComputer proficiency as well as the ability to master new software programs.Experience working in a GMP environment is preferred.Demonstrated success working in a high-performing, business results driven environment.BenefitsHealthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics.Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.Synectics is an equal opportunity employer.