HPLC Scientist - ADTG

Eurofins USA PSS Insourcing SolutionsLexington, MA
11d$31 - $34Onsite

About The Position

Contributes as part of a team of AD scientists towards execution of various analytical methods to support biological therapeutic product release and characterization testing in a compliance-based environment. Independently performs routine testing such as but not limited to SEC, CEX, RP, P20, P80, CE (icIEF Maurice), iCE, CE-SDS (Maurice and PA800) - using established Test Methods, including associated protocol/report documentation and presentations. Conducts work in compliance with cGMP/GLP, safety and regulatory requirements. Responsible for working on other non-lab-based tasks from time to time if assigned. Demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives. Demonstrate HPLC, UPLC and/or CE troubleshooting capabilities.

Requirements

  • Bachelor’s in Cell and Molecular Biology, Analytical chemistry, Biochemistry, Pharmaceutical, or other science related degree concentration with 2+ years of hands-on experience with HPLC/UPLC.
  • Candidates with Master’s degree in Cell and Molecular Biology, Analytical chemistry, Biochemistry, Pharmaceutical, or other science related degree concentration, can be considered provided they have equivalent 6+ months of directly relevant internship experience with HPLC/UPLC.
  • Knowledge of principles of HPLC/UPLC/CE and theories of relevant techniques and basic understanding of industry practices and standards required.
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.

Responsibilities

  • Contributes as part of a team of AD scientists towards execution of various analytical methods to support biological therapeutic product release and characterization testing in a compliance-based environment.
  • Independently performs routine testing such as but not limited to SEC, CEX, RP, P20, P80, CE (icIEF Maurice), iCE, CE-SDS (Maurice and PA800) - using established Test Methods, including associated protocol/report documentation and presentations.
  • Conducts work in compliance with cGMP/GLP, safety and regulatory requirements.
  • Responsible for working on other non-lab-based tasks from time to time if assigned.
  • Demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives.
  • Demonstrate HPLC, UPLC and/or CE troubleshooting capabilities.

Benefits

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