Kilo Lab Pharmaceutical Technician (API/ADC)

Bristol Myers Squibb; New Brunswick (NJ); On-site; USD 48,000 - 68,000; Full time

Job summary

Bristol Myers Squibb invites applications for a Permanent Pharmaceutical Development Technician in the New Brunswick site. The role focuses on maintaining cleanliness, staging materials, and supporting scientists in the Kilo Lab while performing unit operations and data collection under cGLP and cGMP.

Qualified candidates typically hold a two-year science Associate degree or equivalent, with lab experience and proficiency in SAP, DeltaV, and MS Office.

Qualifications

• Two-year Associate Degree in science or equivalent.
• Practical lab experience, especially with API manufacturing.
• cGMP experience in pharma preferred.
• Attention to detail is critical for compliance and safety.
• Proficiency with SAP, DeltaV, and MS Office.

Responsibilities

• Support Kilo Lab Operations with process scale-up.
• Set up, operate, sample, and data-acquire from process equipment.
• Execute unit operations: reaction, distillation, drying, filtration, etc.
• Maintain and read process controls and document data per cGLP/cGMP.
• Ensure safety, containment, and proper handling in high-potency areas.

Skills

Attention to detail

Independent work

Team collaboration

Oral communication

Flexibility

Education

Two-year Associate Degree in science

Partial BA in science or equivalent

Tools

SAP

DeltaV

Microsoft Office

Job description

Bristol Myers Squibb invites applications for a Permanent Pharmaceutical Development Technician in the New Brunswick site. The role focuses on maintaining cleanliness, staging materials, and supporting scientists in the Kilo Lab while performing unit operations and data collection under cGLP and cGMP.

Qualified candidates typically hold a two-year science Associate degree or equivalent, with lab experience and proficiency in SAP, DeltaV, and MS Office.