Quality Control Analyst

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 in Massachusetts to support validation, testing, and reporting of in-process, release, and stability samples.

You will perform tests (flow cytometry, cell counting, culture, sterility, LAL, Visual Inspection) and ensure data integrity in a cGMP environment. The role requires a Bachelor's in a related science and 2–6 years of GMP/pharma lab experience, with attention to detail and strong teamwork.

Qualifications

• Minimum a Bachelor's degree in biology, chemistry, biochemistry, or related field.
• 2–6 years of GMP/pharma/biopharma lab experience required.
• Experience with the listed methodologies in QC environment.

Responsibilities

• Support analytical testing including flow cytometry, cell counting, cell culture, sterility, endotoxin, and visual inspection.
• Perform technical reviews of raw data and record results accurately.
• Maintain lab records and data in paper and electronic systems.
• Conduct routine lab and equipment maintenance duties.
• Troubleshoot analytical methods and participate in Quality Events (Deviations, OOS).
• Collaborate with team to ensure cGMP/cGDP compliance.

Skills

cGMP compliance

Laboratory techniques

Spreadsheet/Word

Team player

Attention to detail

LIMS experience

Electronic instrument software

Electronic lab notebook

Education

Bachelor's degree in science

Tools

LIMS

Electronic instrument software

Electronic lab notebook

Job description

Status: Accepting Candidates

About the role

The Quality Control Specialist is responsible for supporting a variety of analytical functions that occur in the Quality Control (QC) department supporting validation, testing, and reporting of in-process, release, and stability samples. This role also helps ensure activities occur in an efficient and cGMP compliant manner.

Responsibilities

• Typical test methods performed include, but are not limited to, flow cytometry, cell counting, cell culture, sterility (BACT), endotoxin (LAL), and Visual Inspection testing.
• Performs technical reviews of raw data.
• Records test results and maintain raw data and accurate laboratory records on paper and in electronic systems.
• Performs general lab and equipment maintenance duties.
• Performs other duties as assigned.
• Troubleshooting analytical methods and participating in Quality Events (Deviations, OOS)

Knowledge and Skills:

• Performs tasks with strict adherence to cGMP and cGDP principles.
• Has an understanding of basic laboratory equipment and practices.
• Is proficient in the use of spreadsheets and word processing software.
• Is dependable and able to work well within a team.
• Is interested in learning new things. Open to change.
• Is optimistic and displays a positive attitude even during periods of adversity.
• Shows initiative; acts independently with management approval.
• Possesses a high attention to detail.
• Experience with electronic lab notebook (LIMS), and demonstrated ability to work with electronic instrument software

Qualifications

• A minimum of a Bachelor's degree in related field of science is required (Biology, Chemistry, Biochemistry, etc).
• 2-6 years of experience in the GMP pharmaceutical/biopharmaceutical industry
• Demonstrated laboratory experience in multiple methodologies listed above

Compensation (MA Pay Transparency):

• $40–$50/hr (W-2)
• Final rate within the posted range depends on qualifications and interview outcomes.