Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap - Right Talent - Right Time - Right Place - Right Price and acting as a Career Coach to our consultants.
Job Title:QC Associate
Location: Bothell, WA 98021
100% onsite
Duration: 12 months contract (Possible for Extension Based on Performance and/or Budget)
Work hours: 40 hrs/week
Schedule: Wed-Sat 06:00 AM - 04:30 PM PST
Top Skills: • BS in Scientific Discipline, preferably Microbiology • Computer proficiency • Regulated industry experience • Strong communication skills • Demonstrated success working in a high performing, results driven environment
Job Summary:
The 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.
Education:
Bachelor's Degree in a Scientific Discipline (Required), Microbiology preferred
Experience:
0-3 years of experience in a regulated industry, or an equivalent combination of education and experience
Knowledge, Skills, and Abilities • Ability to work in a high paced team environment, meet deadlines, and prioritize work from multiple projects. • Strong analytical and communication skills. • Computer 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.
Responsibilities: • Perform or support cGMP lot release, in-process, and stability testing using various software packages. • Ensure timely completion of testing and tasks as assigned. • Support assay transfer and method validation of by executing cross-site validation protocols and providing data to support final reports. • Identify opportunities for continuous improvements. • Maintain instrumentation and equipment preventative maintenance and supporting documentation in a cGMP compliant manner. • Assist in the implementation of new assay methodologies and the associated instrumentation. • Identify and support initiation of Deviations, CAPAs and Laboratory Investigations.
Working Conditions:
While performing the duties of this job, the employee is 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 magnets. • May work in areas with exposure to vapor phase liquid nitrogen. • Must have ability to work assigned shift (Day, Night, Weekends and/or holidays). • 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.