GMP Quality Control Analyst – Precision Lab

JMD Technologies Inc.; Boston (MA); On-site; USD 55,000 - 69,000; Full time

Job summary

JMD Technologies Inc. is seeking a Quality Control Specialist to support analytical functions in the QC department, including validation, testing, and reporting of in-process, release, and stability samples.

The role ensures activities are conducted efficiently and in a cGMP compliant manner. Responsibilities include executing tests (flow cytometry, cell counting, culture, sterility, endotoxin, and Visual Inspection), reviewing data, and maintaining records both on paper and electronically.

Qualifications

• Bachelor's degree in a related science is required.
• 2–6 years of GMP pharmaceutical/biopharmaceutical experience.
• Experience with multiple listed methodologies in QA labs.

Responsibilities

• Supports validation, testing, and reporting of in-process, release, and stability samples.
• Performs technical reviews of raw data and records test results.
• Maintains raw data and laboratory records in paper and electronic systems.
• Performs general lab and equipment maintenance duties.
• Troubleshoots analytical methods and participates in Quality Events (Deviations, OOS).

Skills

cGMP compliance

lab equipment knowledge

LIMS experience

attention to detail

teamwork

Excel/Word proficiency

adaptability

Education

Bachelor's degree in biology/chemistry/biochemistry

Tools

LIMS

Electronic instrument software

Job description

JMD Technologies Inc. is seeking a Quality Control Specialist to support analytical functions in the QC department, including validation, testing, and reporting of in-process, release, and stability samples.

The role ensures activities are conducted efficiently and in a cGMP compliant manner. Responsibilities include executing tests (flow cytometry, cell counting, culture, sterility, endotoxin, and Visual Inspection), reviewing data, and maintaining records both on paper and electronically.