Pr. Bioassay Scientist at Eurofins

Columbia, Missouri, United States -

Full Time

Start Date

Immediate

Expiry Date

29 Jun, 26

Salary

0.0

Posted On

31 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Method Establishment, Validation, cGMP Guidelines, ELISAs, Multiplex ELISAs, Electrochemiluminescence, Data Analysis, Troubleshooting, Instrument Calibration, Mentoring, Regulatory Trends, Technical Writing, Data Processing, Report Generation, LEAN Initiatives, Client Consultation

Industry

Medical and Diagnostic Laboratories

Description

Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Job Summary: Eurofins BPT-Columbia is looking for a Pr. 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):  Perform routine, non-routine and complex analyses; instrumental analyses; including calibration and troubleshooting/repair of instruments independently  Guide and mentor junior staff to successfully complete projects and grow technical knowledge  Do independent research into regulatory trends and technical advances  Be a technical resource for internal problems throughout Columbia BPT  Provide support for corporate initiatives through BPT network  Provide coverage for management when needed  Document testing, observations, deviations, and results clearly and completely, and in compliance with regulatory requirements – striving to minimize errors  Understand and perform calculations as required by test methods  Understand and utilize computers for information access, calculations, and report preparation  Read and understand analytical procedures (compendial and client supplied) and internal SOP’s  Assist with onboarding new instrumentation, including performing/reviewing IQ/OQ/PQ data or qualifications  Provide consultation for clients  Demonstrate technical writing skills and complete investigations independently  Demonstrate leadership qualities including - Effective communication - Display confidence - Demonstrate motivation and take initiative to Follow through on assignments  Process/review data, generate/review reports, and evaluate data  Suggest and implement lab improvements or modify existing processes to maximize quality and productivity; support and drive LEAN initiatives  Support or identify speaking or publishing opportunities and assist with driving to publication or presentation  Performs other duties as assigned Qualifications Minimum Qualifications: Bachelor’s degree in chemistry, biochemistry, or biology and 5 years of experience working in a cGMP laboratory OR Master’s 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, working Monday-Friday, 8:00 a.m.-4:30 p.m., plus any additional hours as needed. Candidates currently living within commutable distance to Columbia, MO are encouraged to apply. 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.

Responsibilities

The Principal Scientist will act as a subject matter expert in testing Drug Substances and Drug Products, performing method establishment and validations under cGMP guidelines using techniques like ELISAs and ECL methodologies. Responsibilities also include guiding junior staff, conducting independent research into regulatory trends, and ensuring all testing documentation complies with regulatory requirements.