Position Title: Quality Control Analyst Work Location: Lexington, MA 02421 Assignment Duration: 6+ Months Work Schedule: 08:00 AM – 05:00 PM Work Arrangement: 100% Onsite
Position Summary:
Assist in document authoring/ revision and approval (protocols, test methods, SOPs) and other routine laboratory activities supporting the lab as 079 activities are completed by the biochem team.
Background & Context:
This role supports the daily operations of the QC Raw Materials department, whose primary responsibility is the testing and release of raw materials for GMP use in manufacturing.
In this role, the primary responsibility for the individual in this position is to assist in instrument/method projects with some supervision. The projects may require attending meetings based on the specific project, document writing/revising to ensure compliance with regulations and quality control practices.
The person in this role may also be asked to revise documents to assist in the daily operations of the team.
Key Responsibilities:
Executing experiments and procedures as detailed by lab manager and staff. (75% of time)
Writing /revising documents procedures and validation documentation. (25% of time)
Qualification & Experience: Essential:
Minimum Bachelor’s degree in Chemistry/Biology/Biochemistry.
Desired:
Experience in a laboratory environment is preferred.
Experience with Matlab or other chemometric software.
Note: This is not a chromatography focused role, techniques to be used will be FT-NIR with associated chemometric software. Some FTIR and potential wet chemistry methods may also be performed.
Applicant Notices & Disclaimers
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At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws.This position's pay range is $32.00/hr - $35.90/hr.
