Senior Analyst I, Quality Control Chemistry

  • Woburn, MA
  • Posted 6 days ago | Updated 8 hours ago

Overview

On Site
Contract - W2

Skills

Senior Analyst I
Quality Control Chemistry

Job Details



Our Life Sciences client is hiring a Senior Analyst I, Quality Control Chemistry on a one-year contract basis near Boston, MA.


The Senior Analyst will specifically support the gene therapy program and will also work on data trending, invalid assays investigations, quality events (investigations, deviations, Change control, CAPAs).


Responsibilities



  • Execute analytical test methods to support product release and stability of AAV products using different analytical techniques (e.g. HPLC, LCMS, AUC, UV, CE-SDS, compendia methods like Osmolality, pH, Sub visible particulates and Appearance)

  • Review and approval of cGMP analytical data for release and stability testing from chemistry analytical test methods

  • Supports and leads QC Chemistry laboratory operations (ex. Instrument qualification and maintenance. Housekeeping, qualify critical reagents, etc).

  • Author and support quality events; Change controls, Deviation, CAPA, OOS Investigation, as needed.

  • Write, prepare, and present technical data, technical reports, and standard operating procedures (SOPs), Method transfer/ validation protocol, Method transfer/ validation report for internal and external methods.

  • Method Transfer / Validation of QC chemistry methods at internal and external laboratory.

  • Model leadership behaviors and mentor/train junior staff

  • The job responsibilities may change as needed to support activities relevant to the clinical phase.


Qualifications:



  • Experience working in the cGMP QC lab of the pharmaceutical or biopharmaceutical industry is a must.

  • BS/MS Analytical Chemistry, Biochemistry, Biophysics, or a related discipline with at least 5 years of experience working in a cGMP environment.

  • Experience analyzing nucleic acids, virus capsids, antibodies, and/or other biologics materials using HPLC/UPLC, LCMS, AUC, UV- Vis, CE-SDS is strongly preferred.

  • Experience working with external contract labs (CMOs, CROs) is a plus.

  • Strong collaboration and team-working skills.

  • Strong communication, interpersonal and organizational skills.

  • Proven ability to work independently and effectively plan and organize work activities and prioritize task completion to meet schedules and deadlines.

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