Avecia Pharma
Research Scientist I, Analytical Development
Avecia Pharma, Milford, Massachusetts, us, 01757
Research Scientist I, Analytical Development
Sep 9, 2024Regular Full TimeAbout this opportunity:
The Research Scientist I is responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides.Key Responsibilities:Execute testing per method or protocol for development, qualification, verification, validation, and transfer of analytical methods.Analyze test samples, process data, and report results with minimal errors to support research and development primarily focused on oligonucleotides.Provide analytical support to Process Development and Manufacturing.Design and perform method development experiments.Perform GDP and technical peer review.Author technical documentation (e.g., methods, procedures).Provide technical leadership in analytical project meetings.Provide basic-level training in lab techniques and procedures.Plan, track, and execute tasks to deliver project results on time.Communicate with clients and elevate issues to project team leader.Contribute to department objectives for continuous improvement and technical excellence.Contribute to a positive work atmosphere.Required Skills/Abilities:BA/BS with 2+ yrs. of related experience or MS with 1+ yrs. of related experience.Analytical chemistry knowledge including theory and application of fundamental, chromatographic, and spectroscopic techniques for identification, purity, and assay of various analytes.Operate and troubleshoot available instruments such as HPLC and MS.Independently learn new instruments and techniques.Apply undergraduate general, organic chemistry, and analytical chemistry to creatively solve problems.Intermediate Word, Excel, and PowerPoint.Perform common algebraic and statistical calculations correctly.Proficient in technical writing and presentations to internal sites.Author and revise laboratory SOPs.Competency to think strategically and conceptually to apply quality by design principles when designing experiments.Knowledge and application of cGMPs and regulatory guidance documents.
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Sep 9, 2024Regular Full TimeAbout this opportunity:
The Research Scientist I is responsible for meeting the analytical testing requirements to support research and development projects primarily focused on oligonucleotides.Key Responsibilities:Execute testing per method or protocol for development, qualification, verification, validation, and transfer of analytical methods.Analyze test samples, process data, and report results with minimal errors to support research and development primarily focused on oligonucleotides.Provide analytical support to Process Development and Manufacturing.Design and perform method development experiments.Perform GDP and technical peer review.Author technical documentation (e.g., methods, procedures).Provide technical leadership in analytical project meetings.Provide basic-level training in lab techniques and procedures.Plan, track, and execute tasks to deliver project results on time.Communicate with clients and elevate issues to project team leader.Contribute to department objectives for continuous improvement and technical excellence.Contribute to a positive work atmosphere.Required Skills/Abilities:BA/BS with 2+ yrs. of related experience or MS with 1+ yrs. of related experience.Analytical chemistry knowledge including theory and application of fundamental, chromatographic, and spectroscopic techniques for identification, purity, and assay of various analytes.Operate and troubleshoot available instruments such as HPLC and MS.Independently learn new instruments and techniques.Apply undergraduate general, organic chemistry, and analytical chemistry to creatively solve problems.Intermediate Word, Excel, and PowerPoint.Perform common algebraic and statistical calculations correctly.Proficient in technical writing and presentations to internal sites.Author and revise laboratory SOPs.Competency to think strategically and conceptually to apply quality by design principles when designing experiments.Knowledge and application of cGMPs and regulatory guidance documents.
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