Quality Control Analyst I - Biotech Lab (Onsite)

Vericel Corporation; Burlington (MA); On-site; USD 44,000 - 50,000; Full time

Job summary

Vericel Corporation in Burlington, MA is hiring a Quality Control Analyst I to perform routine testing of raw materials, in-process, DP and stability samples in the QC lab, following SOPs and cGMP guidelines. This on-site role requires Sunday-Thursday schedule with some days in Cambridge during facility transition.

You will operate instruments like pH meters, UV/Vis spectrophotometer, plate reader; conduct microbial and environmental monitoring; review QC data; report out-of-spec results;

Qualifications

• BS or AS in a science field with cGMP lab experience.
• 2-4 years’ industry experience for HS diploma path.
• Basic working knowledge of cGMP regulations.

Responsibilities

• Perform routine QC testing for raw materials, in-process, drug product and stability samples.
• Perform cell culture microbial and/or molecular assays as needed.
• Environmental Monitoring and utilities testing.
• Review QC data and provide summaries to management.

Skills

Environmental monitoring

Microbial testing

Data management (LIMS)

Lab skills

Education

Bachelor or AS in science with cGMP lab experience

HS Diploma with related experience

Tools

Outlook

MS Word

Excel

LIMS

Job description

Vericel Corporation in Burlington, MA is hiring a Quality Control Analyst I to perform routine testing of raw materials, in-process, DP and stability samples in the QC lab, following SOPs and cGMP guidelines. This on-site role requires Sunday-Thursday schedule with some days in Cambridge during facility transition.

You will operate instruments like pH meters, UV/Vis spectrophotometer, plate reader; conduct microbial and environmental monitoring; review QC data; report out-of-spec results;