Document Control Analyst Lenox Executive Search Lexington, MA Job Details Contract $35.00 - $40.13 an hour 18 hours ago Qualifications Biology MATLAB Biochemistry Document control experience within pharmaceutical industry Bachelor's degree Compliance documentation Chemistry GMP for research safety and compliance

Full Job Description Job Description:

- Assist in document authoring/ revision and approval (protocols, test methods, SOPs) and other routine laboratory activities supporting the lab as activities are completed by the biochem team. •MUST have good Documentation skills with Lab and GMP experiene. 100% Onsite Primary Duties 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. Responsibilities Job duty and Description Executing experiments and procedures as detailed by lab manager and staff. Writing /revising documents procedures and validation documentation

Education and Experience Requirements Essential :

Minimum Bachelor's degree in Chemistry/Biology/Biochemistry.

Desired :

Experience in a laboratory environment is preferred. Experience with Matlab or other chemometric software.

Pay:

$35.00 - $40.13 per hour

Experience:

Bachelor's degree in Chemistry/Biology/Biochemistry.: 2 years (Required) Matlab or other chemometric software.: 2 years (Required)

Work Location:

In person