Job Description

Job Responsibilities

• The Sr. Manufacturing Supervisor is responsible for daily GMP manufacturing operations in the DPF, including the assembly, set-up, operation, disassembly, and cleaning of process equipment
• The candidates will be responsible for the production and characterization of human ES/iPS and lymphoid lineage-specific derivatives using standard operating procedures.
• Focus on cGMP operation for generating human cell therapy products for the treatment of cancers and other
• Understanding of and strict adherence to cGMP requirements
• Compliance with all ongoing training requirements
• Following Batch Records, SOPs, policies, and all other relevant work instructions to ensure the successful and compliant operation of the drug product facility
• Interfacing with cleaning staff, Facilities/Operations, Quality, EH&S, Materials Management, and the Release and Stability Laboratory to ensure facility operation
• Entering data into log books and batch records
• Interfacing with computerized systems and automated process equipment

Qualifications

• BSc or MS in Biology, Chemistry, Biochemistry, cell biology
• Previous working experience in Biotech/Pharma utilizing current Good Manufacturing Practices (cGMP)
• Experience with cell culture and cell engineering is preferred
• Previous working experience in stem cell, cell therapy, Immuno-Oncology, or biologics

Job Type: Full-time Pay: $100,000.00 - $130,000.00 per year Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday

Ability to commute/relocate:

• Boston, MA: Reliably commute or planning to relocate before starting work (Required)

Work Location: One location

• Health insurance