QC Analyst II: In-Process & Release Testing

Moderna Therapeutics; Norwood (MA); On-site; USD 63,000 - 101,000; Full time

Benefits offered by this job

Competitive healthcare

Paid time off

Onsite work culture

Job summary

Moderna Therapeutics is seeking an Associate II to perform in-process, release, and stability testing in the Quality Control Chemistry laboratory. The role requires handling analytical equipment, adhering to cGMP and regulatory standards, and supporting special projects as assigned.

Onsite work emphasizes collaboration and precise documentation. The candidate should have a BA/BS in Chemistry and at least two years in a pharmaceutical QC lab, with experience using HPLC/UPLC, UV plate readers, and

Qualifications

• Requires BA/BS in Chemistry or related science and minimum two years of experience in a pharmaceutical QC lab.
• Experience performing in-process, release and stability testing in a cGMP environment is preferred.
• Familiarity with regulatory requirements (FDA, ICH) and GDP data integrity principles.

Responsibilities

• Perform in-process, release and stability testing for materials and products per cGMP requirements.
• Operate analytical instrumentation (HPLC/UPLC, UV, KF, DLS) and document results in LIMS or worksheets.
• Maintain data integrity and comply with GDP; assist with SOPs and method validation.
• Provide general lab support (reagents, samples, maintenance) and participate in investigations as needed.

Skills

Quality control testing

GMP compliance

Analytical testing methods

Education

B.A./B.S. in Chemistry

Tools

HPLC

UPLC

UV plate reader

Dynamic Light Scattering

KF

Osmolality

Job description

Moderna Therapeutics is seeking an Associate II to perform in-process, release, and stability testing in the Quality Control Chemistry laboratory. The role requires handling analytical equipment, adhering to cGMP and regulatory standards, and supporting special projects as assigned.

Onsite work emphasizes collaboration and precise documentation. The candidate should have a BA/BS in Chemistry and at least two years in a pharmaceutical QC lab, with experience using HPLC/UPLC, UV plate readers, and