About the role
Job Description
Responsibilities include but are not limited to:
* Perform verification of data and confirm resolution of issues identified * Perform cell culture, cell-based bioassay, and surrogate bioassays such as ligand-binding ELISA assays in plate-based formats in a GMP environment and other lab tasks for training and as needed. * Anticipate quality events or issues and elevate them to appropriate management attention immediately * Independently engage and collaborate with coworkers, customers, and management within a cGMP environment * Must be able to identify problems and know when to solve proactively and seek advice * Contribute and participate in investigations, as needed * Support regulatory and client inspections, as needed
Qualifications
* Bachelor’s degree in life science concentration (chemistry, biology, or related fields) and 2 to 4 years of directly related industry experience or a MS degree in a life science concentration (chemistry, biology, or related fields) and up to 2 years of directly related industry experience. * Proficiency in cGMP and FDA regulated clinical services laboratory environment * Strong computer, scientific, and organizational skills * Excellent written and oral communication with attention to detail * Capability to work well on a team and be able to troubleshoot and problem solve in cross functional team setting
Additional Information
* Position is full-time, working Monday-Friday 8:00 a.m.-5:00p.m overtime as needed * Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply. * Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays * Authorization to work in the United States indefinitely without restriction or sponsorship
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.