Cell Therapy / CGT - Associate, QC

JMD Technologies Inc.; Boston (MA); On-site; USD 38,572 - 41,328; Full time

Job summary

JMD Technologies Inc. is looking for a Cell Therapy / CGT Associate to support Quality Control testing activities in Boston, Massachusetts. The ideal candidate will have hands-on QC lab experience and a Bachelor's degree in a life science.

The role involves performing tests using Flow Cytometry, qPCR, and ELISA, among other methods. Compensation is estimated at $28–$30/hr based on skills and experience.

Qualifications

• 1-2 years of QC laboratory experience, including internships.
• Hands-on experience with sterile laboratory practices.
• Knowledge of regulated lab workflows.

Responsibilities

• Perform QC testing using various methods.
• Execute testing following cGMP/cGDP standards.
• Review raw data and maintain laboratory records.

Skills

Flow Cytometry

qPCR

ELISA

Aseptic technique

Education

Bachelor’s degree in Biology, Biotechnology, Biochemistry or related Life Sciences

Tools

cGMP documentation

cGDP documentation

Job description

Cell Therapy / CGT - Associate, QC

Employment Type: Contract

Status: Accepting Candidates

About the role

Join a Quality Control team supporting critical Cell Therapy / CGT testing activities for in-process, release, and stability samples. This role is ideal for candidates with hands‑on QC lab experience in regulated biotech environments.

Key Responsibilities

• Perform QC testing using Flow Cytometry, qPCR, ELISA, cell counting, sterility, gram stain, and endotoxin (LAL) methods
• Execute testing of in-process, release, and stability samples following cGMP / cGDP standards
• Review raw data, document test results, and maintain accurate laboratory records
• Support QC data tracking, trending, and technical documentation activities
• Perform general laboratory and equipment maintenance
• Collaborate with cross-functional teams while adhering to strict quality and compliance requirements

Qualifications

• Bachelor’s degree in Biology, Biotechnology, Biochemistry, or related Life Sciences
• 1–2 years of QC laboratory experience (relevant co‑op/internship experience considered)
• Hands‑on experience with aseptic technique and sterile laboratory practices
• Experience with biologics testing, cell‑based assays, or Cell Therapy / CGT environments
• Knowledge of cGMP / cGDP documentation and regulated lab workflows
• Experience with Flow Cytometry, ELISA, or qPCR strongly preferred

Compensation (MA Pay Transparency)

• Estimated hourly range: $28–$30/hr (W-2).
• Final rate within this range will be based on skills, experience, and interview results.