Cell Therapy Manufacturing Specialist - Night Shift

Cellares; Bridgewater (MA); On-site; USD 27,552 - 61,992; Full time

Benefits offered by this job

Competitive base salaries

Medical, Dental and Vision plans

401(k) Matching

Onsite lunches

Job summary

Cellares in Bridgewater, MA is seeking a Night Shift Cell Therapy Manufacturing Specialist to support our Process Sciences team in advancing our cell therapy platform. The role focuses on manufacturing operations and day-to-day lab duties in a fast-paced, compliant environment.

You will execute GMP-driven processes, follow SOPs, and collaborate with engineering and quality teams to drive robust production, continuous improvement, and safe operations on the manufacturing floor.

Qualifications

• Bachelor’s degree or diploma in a scientific or related field is required.
• 1+ years of biotech/biopharma experience in cGMP Operations, preferably cell/gene therapy.
• Adherence to cGMPs and company safety policies is required.
• Experience following SOPs, batch records, and GMP documentation.
• Excellent verbal, written, and interpersonal communication skills.

Responsibilities

• Perform routine procedures following SOPs, batch records, and protocols.
• Execute manufacturing processes in R&D and GMP environments.
• Support reagent preparation, leukopak processing, and sample testing.
• Maintain clean room and laboratory activities, including audits and equipment maintenance.
• Train and mentor new manufacturing associates on aseptic techniques.
• Review documents for accuracy and ensure batch records are submitted on time.

Skills

Analytical thinking

Problem-solving

Interpersonal communication

Self-motivated

Growth mindset

Safety-conscious

Team collaboration

Education

Bachelor's degree or diploma in a scientific field

Tools

Drug product equipment

Job description

Cellares in Bridgewater, MA is seeking a Night Shift Cell Therapy Manufacturing Specialist to support our Process Sciences team in advancing our cell therapy platform. The role focuses on manufacturing operations and day-to-day lab duties in a fast-paced, compliant environment.

You will execute GMP-driven processes, follow SOPs, and collaborate with engineering and quality teams to drive robust production, continuous improvement, and safe operations on the manufacturing floor.