Associate I, Cell Therapy Manufacturing

Vericel Corporation; Burlington (MA); On-site; USD 33,000 - 36,000; Full time

Job summary

Vericel Corporation in Burlington, MA is seeking an Associate I, Cell Therapy Manufacturing to execute manufacturing steps for commercial cell therapy products. The role is onsite in Burlington with transitional time in Cambridge; training weeks 6:30 AM–3:00 PM, then shifts 6:30 AM–5:00 PM (Sun–Wed or Wed–Sat).

The candidate will perform aseptic cell culture operations, document in batch records, and maintain inspection-ready facilities while growing with the team in a regulated environment.

Qualifications

• Bachelor’s degree (Life Sciences or related field) required or HS diploma/GED with 2+ years of cGMP experience.
• Excellent communication skills, written and verbal.
• Experience with Microsoft Office suite.

Responsibilities

• Perform manufacturing procedures inside a manufacturing clean room in accordance with SOPs, cGMPs and safety regulations.
• Qualified to perform aseptic manipulations of cell culture operations.
• Make cell-culture decisions based on observations and written procedures.
• Document operations in Electronic Batch Records and log sheets per cGMPs and SOPs.
• Maintain manufacturing areas in inspection-ready state; perform clean room sanitization.
• Record equipment and facility metrology data; report out-of-spec readings.
• Work independently after training; organize and manage time effectively.
• Collaborate with team; promote positive interactions and cooperation.
• Follow Vericel safety procedures and guidelines.
• Assist in reviewing/revising production documents (SOPs, electronic records).
• Identify and report deviations and contribute to deviation investigations.
• Cross-train and qualify in at least one core competency (e.g., 3T3, Media Prep, D365 ERP, TrackWise, Veeva).
• Other duties as assigned.

Skills

Excellent communication skills

cGMP experience

Microsoft Office proficiency

Education

Bachelor’s degree (Life Sciences or related field)

HS diploma/GED with 2+ years of cGMP experience

Tools

Microsoft Office

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Associate I, Cell Therapy Manufacturing

Regular Full-Time Burlington, MA, US

At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment to innovation, patient-centered focus, and scientific excellence drives us to develop groundbreaking treatments including MACI (knee cartilage repair), Epicel and Nexobrid (burn care).

Position Summary:

Responsible for the execution of process steps to manufacturecommercial cell therapy products meeting internal and regulatory requirements.

Schedule: This position is onsite at our new Burlington, MA office, with some time required in our Cambridge office during the transition to the new facility.

During the first 3–5 months of training, you will be onsite in Burlington Monday through Friday from 6:30 AM to 3:00 PM. Upon completion of training, you will transition to a shift schedule based on business needs, with current shifts being Sunday through Wednesday and Wednesday through Saturday, from 6:30 AM to 5:00 PM.

Key Responsibilities:

• Perform manufacturing procedures inside a manufacturing clean room in accordance with established SOPs, cGMPs, and safety regulations.
• Qualified to perform aseptic manipulations of cell culture operations.
• Able to make cell-culture decisions based on cell observations and guidelines in written procedures.
• Documentall operations in Electronic Batch Records and log sheets according to cGMPs and established SOPs.
• Maintain manufacturing-controlled areas in an inspection ready state. Perform clean room equipment sanitization.
• Record equipment and facility metrology data to ensure the equipment operates within specifications. Report out of specification readings to production management.
• Able to work independently upon completion of training. Demonstrate the ability to organize, plan and manage time to effectively complete daily tasks. Be receptive to feedback and guidance from manager and other more experienced staff.
• Build and grow our teams through collaboration and positive interactions. The ability to cooperate with others in a team environment will be critical to your and our combined success.
• Practice safe work habits and adhere to Vericel’s safety procedures and guidelines.
• Assist in reviewing and revising production documents (SOP’s and electronic records).
• Ability to identify and report deviations and contribute to deviation investigations.
• In addition to being fully qualified in MACI or Epicel, cross train and qualify in at least one core competency e.g. 3T3, Media Prep, D365 ERP, TrackWise, Veeva.
• Other duties as assigned.

Basic Qualifications:

• Bachelor’s degree (Life Sciences or related field) with 0 - 2 years of experience working in a cGMP environment in the biotechnology/pharmaceutical industry or HS diploma/GED with 2+ years of cGMP experience.
• Excellent communication skills, written and verbal.
• Experience with Microsoft Office suite.

Preferred Qualifications:

• Biotechnology certificate that includes hands-on laboratory courses.
• Experience in small scale tissue culture processing.
• Experience working within a regulated environment that is frequently audited by internal and external Agencies, such as the FDA and ISO

Working Conditions & Physical Demands:

• May be required to sit for long periods of time while performing cell culture operations.
• Must be able to lift, carry, push and pull up to 50 lbs.
• Ability to work 1 weekend day per week.
• Rotating holiday coverage.
• Ability to gown and gain entry to manufacturing areas.

Why Vericel?

• Cutting-Edge Science: Work with a leading regenerative medicine product that is transforming patient care
• Career Growth: Be a part of a growing organization with opportunities to expand your impact
• Collaborative Culture: Work alongside a team of dedicated professionals who are passionate about improving lives

The hourly wage range Vericel reasonably and in good faith expects to pay for this position at the time of this posting is $24-$26 an hour.

The actual salary offered will be determined based on factors such as the candidate’s qualifications, experience, and skills. Bonus, incentive pay, equity and benefits may be provided in addition to the base compensation listed above.

In accordance with Massachusetts law, Vericel provides the pay range that it reasonably and in good faith expects to pay for a particular and specific employment position at the time of posting or offer. This range is subject to change based on business needs, market conditions, and individual qualifications. Employees and applicants may request the pay range for their position or for a position to which they are applying. Retaliation for making such a request is strictly prohibited.

EEO Statement

All applicants will receive consideration for employment without regard to their race, color, religion, sex, national origin, sexual orientation, gender identity, or protected veteran status and will receive consideration for employment and will not be discriminated against on the basis of disability. Vericel Corporation is an Equal Opportunity/Affirmative Action Employer.

Vericel Corporation is VEVRAA federal contractor and desires priority referrals of protected veterans for job openings at all locations within the state.