GMP QC Lab Analyst – Raw Materials Release

The Fountain Group; Lexington (MA); On-site; USD 110,415,000 - 114,203,000; Part time

Job summary

The Fountain Group is seeking a Quality Control Analyst in Lexington, MA to support daily QC operations focused on testing and release of raw materials for GMP manufacturing.

The role requires hands-on laboratory experience in a GMP environment, experience executing experiments and analytical procedures, and proficiency with QC documentation such as SOPs, test methods, and validation documents. A Bachelor's degree in Chemistry, Biology, Biochemistry, or a closely related field is required.

Qualifications

• Hands-on laboratory experience in a QC or GMP environment.
• Experience executing laboratory experiments and analytical procedures.
• Experience with QC documentation, including SOPs, test methods, protocols, or validation documents.
• Knowledge of GMP laboratory practices and raw material testing/release processes.

Responsibilities

• Support daily QC Raw Materials laboratory operations focused on testing and release of raw materials for GMP manufacturing use.
• Execute laboratory experiments and procedures under the direction of the lab manager and QC staff.
• Assist with instrument and analytical method projects with appropriate supervision.
• Author and revise protocols, test methods, SOPs, validation documents, and other QC documentation.
• Participate in project meetings and support documentation activities required for regulatory and quality control compliance.
• Perform routine laboratory activities supporting QC operations and ongoing projects.

Skills

Hands-on QC in GMP environment

Execute lab experiments

QC documentation (SOPs, test methods,/

GMP practices & raw material testing

Education

Bachelor's degree in Chemistry/Biology/Biochemistry or related field

Tools

MATLAB

Job description

The Fountain Group is seeking a Quality Control Analyst in Lexington, MA to support daily QC operations focused on testing and release of raw materials for GMP manufacturing.

The role requires hands-on laboratory experience in a GMP environment, experience executing experiments and analytical procedures, and proficiency with QC documentation such as SOPs, test methods, and validation documents. A Bachelor's degree in Chemistry, Biology, Biochemistry, or a closely related field is required.