Senior Biotech GMP Technician & Automation Mentor

BioSpace; Framingham (MA); On-site; USD 65,000 - 90,000; Full time

Job summary

Sanofi in Framingham, MA is hiring a Senior Manufacturing Technician for a 12-hour rotating shift in a large-scale cGMP biologics facility. You will perform complex tasks under general guidance, following manufacturing instructions and GMPs to ensure compliant operations.

The role emphasizes safety, documentation, equipment operation, process improvements, and collaboration with QA, QC, and Manufacturing Engineering.

Qualifications

• High School diploma/GED with a minimum of 1 year of experience in cGxP manufacturing environment.
• Biotech Certificate or Biotech associate's degree with no prior experience.
• Bachelor's degree in Biotech with no prior experience.

Responsibilities

• Maintains a safe working environment and reporting of incidents/accidents to Manufacturing management.
• Effectively demonstrates understanding of GMPs and how they apply to specific responsibilities.
• Follows verbal and written procedures in operating production and equipment and performing processing steps; accurately completes appropriate production documentation.
• Maintains cleanliness and orderliness in process area.
• Ensures production area is stocked with supplies.
• Performs SOP revisions and work order generation.
• Interacts with Quality Assurance, Quality Control, Manufacturing Engineering, MSIT, Validation, etc.
• Utilizes manufacturing knowledge to improve process operations and affect positive change.
• Demonstrates ability to troubleshoot basic mechanical operations.
• Demonstrates knowledge of automation systems (INFOR, MES, ERP, DeltaV).
• Demonstrates general knowledge and practice of aseptic techniques.

Skills

GMP knowledge

Microsoft Office

Troubleshooting

Education

High School Diploma / GED

Biotech Certificate

Biotech Associate degree

Bachelor's in Biotech

Tools

DeltaV

INFOR

MES

ERP

Job description

Sanofi in Framingham, MA is hiring a Senior Manufacturing Technician for a 12-hour rotating shift in a large-scale cGMP biologics facility. You will perform complex tasks under general guidance, following manufacturing instructions and GMPs to ensure compliant operations.

The role emphasizes safety, documentation, equipment operation, process improvements, and collaboration with QA, QC, and Manufacturing Engineering.