Description
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.
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