Bioassay Data Review Specialist
Eurofins Scientific
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- Location
- Indianapolis, IN
- Work style
- On-site
- Job type
- Full time
- Posted
- Oct 7
- 13 days ago
Career path
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About the company
Eurofins Scientific
Biotechnology · 10,001+ employees
What you'll do
- <p><strong>Responsibilities include but are not limited to:  </strong></p><ul><li>Perform verification of data and confirm resolution of issues identified</li><li>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.</li><li>Anticipate quality events or issues and elevate them to appropriate management attention immediately</li><li>Independently engage and collaborate with coworkers, customers, and management within a cGMP environment</li><li>Must be able to identify problems and know when to solve proactively and seek advice</li><li>Contribute and participate in investigations, as needed</li><li>Support regulatory and client inspections, as needed</li></ul>
What you need
- <ul><li>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. </li><li>Proficiency in cGMP and FDA regulated clinical services laboratory environment</li><li>Strong computer, scientific, and organizational skills</li><li>Excellent written and oral communication with attention to detail</li><li>Capability to work well on a team and be able to troubleshoot and problem solve in cross functional team setting</li></ul>
- Education: a bachelor's degree or a postgraduate degree
Key skills
cGMPFDA regulatedcell culturecell-based bioassayligand-binding ELISAorganizational skillswritten and oral communicationattention to detailtroubleshootproblem solve
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Perks
- medical coverage
- dental
- vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation
- holidays
See full description on company page, apply now
Read the full posting here
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
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
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.