Entry Level Laboratory Data Review
Eurofins Scientific
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- Location
- Columbia, MO
- Work style
- On-site
- Job type
- Full time
- Posted
- Oct 13
- 7 days ago
Career path
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About the company
Eurofins Scientific
Biotechnology · 10,001+ employees
What you'll do
- <p><strong>*THIS IS <u>NOT</u> A DATA SCIENCE POSITION*</strong></p><p>Eurofins BPT-Columbia is looking for a <strong>Associate Scientist, Data Review </strong>to<strong> </strong>join our Quality Assurance team located in Columbia, Missouri.  The Quality Assurance Associate position is an entry-level position involved in day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). </p><ul><li>Review scientific reports under cGMP guidelines to ensure regulatory requirements have been met, the data is whole and accurate, and the report is of high quality.</li><li>Assisting with internal audits</li><li>Work closely with lab operations staff on a day-to-day basis and have the authority and responsibility for final report sign-off.</li><li>Other duties as assigned.</li></ul>
What you need
- Requires a bachelor’s degree in a relevant field or comparable coursework, and the ability to work in the US indefinitely without restriction or sponsorship.
- Laboratory or GMP pharmaceutical experience is listed as ideal.
- Education: a bachelor's degree
Key skills
cGMP guidelineslaboratory settingGMP pharmaceutical settingorganizational skillscommunication skillsattention to detailBachelor’s degree
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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
*THIS IS NOT A DATA SCIENCE POSITION*
Eurofins BPT-Columbia is looking for a Associate Scientist, Data Review to join our Quality Assurance team located in Columbia, Missouri. The Quality Assurance Associate position is an entry-level position involved in day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.).
Review scientific reports under cGMP guidelines to ensure regulatory requirements have been met, the data is whole and accurate, and the report is of high quality.
Assisting with internal audits
Work closely with lab operations staff on a day-to-day basis and have the authority and responsibility for final report sign-off.
Other duties as assigned.
The ideal candidate would possess:
Experience in a laboratory setting or GMP pharmaceutical setting.
Good organizational skills; ability to follow direction and good communication skills are required.
Strong computer, scientific, and organizational skills.
Excellent communication (oral and written) and attention to detail.
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
Minimum Qualifications
Bachelor’s degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field or degree with comparable coursework in the above areas.
Ability to work in the US indefinitely without restriction or sponsorship
Working schedule will be Full-Time, First Shift, M-F 8am-4:30pm. Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply. No relocation assistance will be given. 25% travel may be required. This position is NOT remote.
What we Offer:
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
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.