QC Analyst II, cGMP Testing & Stability (Onsite)

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

Benefits offered by this job

Healthcare benefits

Well-being resources

Paid time off

Location-based perks

Job summary

Moderna is seeking an Associate II with cGMP quality control analytical testing experience. This role performs in-process, release and stability testing in the QC Chemistry lab onsite and supports special projects as assigned.

The position requires at least two years of QC laboratory experience in a pharmaceutical setting and a B.A./B.S. in Chemistry or related field. Moderna offers a comprehensive benefits package and an onsite work environment.

Qualifications

• BA/BS in Chemistry (preferred) or other relevant scientific discipline.
• Working experience: at least two years in quality control laboratory in a pharmaceutical company.

Responsibilities

• Perform in-process, release and stability testing for materials and products.
• Operate analytical instruments per SOPs and regulatory requirements.
• Document results using worksheets or LIMS and ensure data integrity.
• Provide general lab support and inventory management.
• Assist with troubleshooting of assay methods and equipment.
• Participate in lab investigations (OOS/OOT/OOE) and CAPAs.

Skills

Quality control

Laboratory testing

Regulatory compliance

Data integrity

Education

BA/BS in Chemistry

Tools

HPLC

UPLC

UV plate reader

KF

Osmolality

Dynamic Light Scattering

Particulate matter analysis

Job description

Moderna is seeking an Associate II with cGMP quality control analytical testing experience. This role performs in-process, release and stability testing in the QC Chemistry lab onsite and supports special projects as assigned.

The position requires at least two years of QC laboratory experience in a pharmaceutical setting and a B.A./B.S. in Chemistry or related field. Moderna offers a comprehensive benefits package and an onsite work environment.