Cell Therapy Manufacturing Specialist

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

Position Summary

Night Shift: 6 PM- 6 AM

We are seeking an innovative and highly motivated Cell Therapy Manufacturing Specialist to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations.

Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.

Responsibilities

• Perform routine procedures following written instructions (SOPs, batch records, solution documents, protocols, etc.)
• Execute manufacturing processes in both an R&D and GMP environments, following protocols and/or standard operating procedures (SOPs)
• Provide user feedback to engineering and process teams, support with requirements gathering and review
• Support reagent preparation, leukopak processing, and sample testing in an R&D and GMP environment
• Contribute to analysis and presentation of technical results at departmental meetings
• Perform routine clean room and laboratory activities including ordering, cleaning, restocking, and equipment qualification/maintenance
• Operate in a controlled GMP environment and perform gowning as per procedure
• Complete required training and ensure compliance with established internal and external control procedures
• Assist in the execution of process, equipment and cleaning validation
• Responsible for revising and originating production records, standard operating procedures, protocols and reports
• Initiate and support the closure of Deviation Reports and CAPAs
• Train and mentor new manufacturing associates on procedures, aseptic techniques, equipment and trouble-shooting skills
• Review in-process and completed documents for accuracy and to make sure batch records are turned in to area management within specified days of completion
• Work with Quality Control, Facilities, Materials Management, Quality Assurance and Validation to complete assignments
• Other duties as assigned

Requirements

• Bachelor’s Degree or diploma in a scientific or related field is required
• 1+ years of experience within the biotech/biopharma industry in cGMP Operations, preferably within cell and gene therapy
• Must know and follow job safety procedures, attend required health and safety training, proactively promote safety at work, and promptly report actual and potential accidents and injuries
• Must comply with the safety policies of the company and site
• Adherence to cGMPs is required at all times during the manufacturing of Cell Therapy products
• Proficiency in Drug Product-related process equipment
• Must have experience following protocols, SOPs, and/or GMP documentation
• Excellent verbal, written, presentation, and interpersonal skills
• Strong analytical and problem-solving skills
• Self-motivated and passionate about advancing the field of cell therapy
• Self-awareness, integrity, authenticity, and a growth mindset
• Desire to be part of a rapidly evolving organization, with compelling technology, and take products and processes to the next level

Compensation

$20 - $45 an hour

Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, and Onsite lunches. All displayed pay ranges are approximate, negotiable, and location dependent.