Cell Therapy Manufacturing Training Specialist

Bristol Myers Squibb

Summit (NJ)

On-site

USD 52,000 - 63,000

Full time

2 days ago
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Benefits offered by this job

Comprehensive benefits
Flexible time off
11 paid holidays
Stock opportunities

Job summary

Bristol Myers Squibb in Summit, NJ is seeking a Specialist, Manufacturing Technical Development to lead the site Manufacturing Training Program and ensure compliant training for staff in aseptic processes.

The role trains staff, develops and administers training solutions, performs ILT/OJT sessions, and collaborates with management and Quality to drive continuous improvement while maintaining cGMP and regulatory standards.

Qualifications

  • Bachelor's degree in Biology, Biochemical Engineering, Chemical Engineering, Biomedical Engineering, or a related field.
  • At least 4 years in a cGMP-regulated biopharmaceutical, biotechnology or pharmaceutical manufacturing environment.
  • At least 4 years in cell therapy manufacturing processes and GMP regulations.
  • At least 2 years delivering training programs in a regulated environment.
  • Advanced proficiency in Microsoft Office (Word, Excel, PowerPoint).
  • Strong organizational, project and time management skills.

Responsibilities

  • Implements training programs meeting regulatory requirements and business needs.
  • Works with management to create a training plan addressing production demands.
  • Conducts ILT and OJT sessions for aseptic processing.
  • Provides trainee feedback and identifies gaps requiring additional training.
  • Maintains training documentation and records.

Skills

Communication skills
Classroom teaching
Interpersonal skills
Aseptic environment
Documentation
Training program design
Cross-department collaboration

Education

Bachelor's degree in Biology or related field

Tools

Microsoft Office

Job description

Bristol Myers Squibb in Summit, NJ is seeking a Specialist, Manufacturing Technical Development to lead the site Manufacturing Training Program and ensure compliant training for staff in aseptic processes.

The role trains staff, develops and administers training solutions, performs ILT/OJT sessions, and collaborates with management and Quality to drive continuous improvement while maintaining cGMP and regulatory standards.

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