Bioassay Scientist Sr. Scientist

Job Summary: Eurofins BPT-Columbia is looking for a Sr.   Scientist  to join our team located in Columbia Missouri. This individual will be a subject matter expert in testing Drug Substances and Drug Products in the Biotech department. The successful candidate will perform method establishment and validations under cGMP guidelines on a diverse set of methods including ELISAs and multiplex ELISAs using electrochemiluminescence (ECL) methodologies. Ability to analyze data and effectively communicate results. Ability to complete work in an agreed upon timeline. Train team upon completion of method establishment and validation.

Responsibilities include (but are not limited to):

• Designing carrying out and performing simple and complex experiments and procedures in accordance with all applicable regulatory (e.g. DEA EPA FDA FIFRA OECD etc.) requirements as defined by protocol method and standard operating procedures (SOPs).
• Perform method establishment and validations on a diverse set of methods including multiplex ELISAs using ECL platforms.
• Analyze data with software including Molecular Devices Softmax Pro and effectively communicate results.
• Train and mentor junior staff.
• Utilize laboratory information management system (LIMS) with proficiency.
• Is able to utilize equipment facilities and personnel to produce sound scientific results in a timely fashion for Eurofins clients.
• Adheres to schedule according to Eurofins or contracting organizations timetable and establishes daily or weekly routines necessary to ensure on-time delivery.

Qualifications :

Minimum Qualifications:

• Bachelors degree in chemistry biochemistry or biology and 5 years of experience working in a cGMP laboratory OR Masters degree and 3 years of experience working in a cGMP laboratory OR PhD and minimum 1 year(s) of experience working in a cGMP laboratory
• Authorization to work in the U.S. without restriction or sponsorship

The Ideal Candidate Would Possess:

• Previous experience working in a CRO/CDMO adhering to cGMP regulations
• Ability to conduct work efficiently analyze data to ensure accuracy and report quality data.
• Industrial experience with method establishment and cGMP validations are highly desirable
• Good problem solving time management communication and interpersonal skills.

Additional Information :

Position is full-time Monday-Friday 8:00 a.m.-4:30 p.m. with additional hours as needed.  Candidates currently living within a commutable distance of Columbia MO are encouraged to apply. 

 We offer excellent full-time benefits including :

• Comprehensive medical coverage
• Life and disability insurance
• 401(k) with company match
• Paid holidays and vacation 
• Dental and vision options.

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Remote Work :

No

Employment Type :

Full-time