Quality Control Analyst (Multiple Openings)

CRISPR Therapeutics•Framingham, MA

3d•$93,000 - $103,000•Onsite

About The Position

Our QC team is looking for enthusiastic individuals to work full time at our state-of-the-art manufacturing facility in Framingham, MA. QC Analyst is a lab based role that is a valuable member of the Quality Control team that will perform in-process, final product, raw material, stability, environmental monitoring, and microbiological testing of novel drug therapies. The successful candidate will perform various biochemical, biophysical, molecular biology, chromatographic, environmental and compendial tests in a GMP environment. In addition, the QC Analyst will support analytical method implementation, transfer and validation projects to support business and clinical needs.

Requirements

Minimum of bachelor’s degree in a relevant scientific area with 3-5 years of relevant industry experience.
Hands-on experience with at least one of the following techniques: flow cytometry, PCR, UPLC Chromatography.
Excellent communication skills, technical writing, and detail oriented.
Good at managing time and evolving priorities in a flexible manner in dynamic environment.

Nice To Haves

Experience with cell culture, aseptic techniques, raw material testing, and/or chromatography preferred.

Responsibilities

Support the implementation and validation of analytical methods to the Framingham facility.
Performs routine in-process, final release, stability, raw material, environmental monitoring, and microbiological testing of CRISPR based products.
Write and/or revise SOPs, test methods, protocols, and reports.
Support QC investigations, OOS, deviations, CAPA implementation, and change controls.
Utilize Laboratory Information Management System to complete the data packets for review by senior members.
Perform other related duties based on business needs.