Potency Bioassay Scientist

Eurofins

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profile Job Location:

Boston, NH - USA

profile Monthly Salary: Not Disclosed
Posted on: 1 hour ago
Vacancies: 1 Vacancy

Job Summary

The Analytical Development team is responsible for developing and implementing new analytical methods applying current methods and optimizing and improving current methods for the characterization of raw materials RNA drug substances and LNP products and programs at various developmental stages. We are seeking a highly skilled passionate and motivated Research Associate / Senior Research Associate to join our Analytical Development team to support analytical development and testing of non-GMP samples for development studies such as comparability assessments process development stability product and process characterization. This role is part of a Technical Operations team that partners closely with Quality Control Quality Assurance Process Development and Analytical Research & Development with aims to advance preclinical gene editing candidates into the clinic and support our growing gene editing pipeline.

Position Responsibilities:

  • Support and execute on activities to develop and qualify phase appropriate methods from the analytical research team intended for a variety of purposes including release and stability testing product characterization high-throughput analysis and characterization of complex raw materials.
  • Perform routine (approximately 60% effort) and non-routine (approximately 40% effort) potency assays.
  • Execution of techniques including sterile tissue culture maintenance of mammalian cell culture preps LNP handling and cell-based or other LNP potency assays.
  • Potential for execution of DNA/RNA extraction from cells PCR/NGS library preparation real time PCR reverse transcription or other techniques as needed.
  • Collect process and analyze experimental data ensuring accurate and timely documentation in electronic notebook.
  • Review interpret and present data within the analytical team and cross-functionally.
  • Author review and revise technical source documents to support phase-appropriate analytical development needs.
  • Maintain laboratory equipment and order critical reagents.
  • Provide technical oversight to guide analytical/QC investigations as needed.
  • Actively collaborate with internal and external process development and quality teams.
  • Other duties as assigned.

Qualifications :

Basic Minimum Qualifications:

  • B.S. degree in biological or biochemical sciences (or related field) with 1 years of relevant laboratory experience. M.S. degree in biological or biochemical sciences (or related field) with relevant laboratory experience.
  • Experience in sterile tissue culture technique and mammalian cell line maintenance including cell handling passaging seeding and banking. 
  • Experience with bioanalytical methods such as cell-based functional assays and ELISA (experience with handling protein DNA and RNA and molecular biology assays is a plus).
  • Experience working with various analytical instrumentation such as cell counters ELISA platforms and plate readers.
  • Experience with ELN software systems such as Benchling.
  • Excellent interpersonal and collaborative skills and the ability to work independently and effectively in a highly dynamic environment.
  • Comfortable communicating highly technical information.
  • Strong organizational and time management skills.
  • Proactive creative and positive attitude.

Preferred Qualifications:

  • Experience with oligonucleotides or lipid nanoparticles.
  • Experience working on potency related testing.
  • Experience working on automation platforms.
  • Experience working with various biophysical instrumentation such as DLS osmometer pH and basic fluorescence-based assays.
  • Ability to present data in team meetings.
  • Knowledge/hands-on experience in analytical method development qualification validation and transfer to GMP environments.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.

Additional Information :

The position is full-time first shift Monday-Friday with overtime as needed. Candidates living within a commutable distance of Boston MA are encouraged to apply.

Excellent full-time benefits include:

  • Comprehensive medical coverage dental and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • Eligibility for yearly goal-based bonus & merit-based increases
  • Compensation: $33.00-$36.00 per hour based on education and past experience.

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.


Remote Work :

No


Employment Type :

Full-time

The Analytical Development team is responsible for developing and implementing new analytical methods applying current methods and optimizing and improving current methods for the characterization of raw materials RNA drug substances and LNP products and programs at various developmental stages. We ...
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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 the environment safer, healthier and more sustainable. From the food you eat to the medicines you rely on, Eur ... View more

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