Parenteral Manufacturing Technician

Bristol Myers Squibb

Manati, Puerto Rico, US
Base: $16.70 - $20.24 ph; bonus/equity: + incentiv...
50% onsite
Parenteral manufacturing equipment operation
Aseptic technique and contamination control
Cgmp and data integrity principles
The Parenteral Manufacturing Technician is responsible for executing routine and critical parenteral drug product manufacturing operations for highly sensitive pharmaceutical and biologic products in a controlled environment

Job Summary

  • The Parenteral Manufacturing Technician is responsible for executing routine and critical parenteral drug product manufacturing operations for highly sensitive pharmaceutical and biologic products in a controlled environment.
  • This role performs equipment setup, changeover, cleaning, line clearance, in-process monitoring, and excipients weighing, in accordance with approved Standard Operating Procedures (SOPs), Safety Policies, and current Good Manufacturing Practices (cGMP).
  • Bristol Myers Squibb offers a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

The Parenteral Manufacturing Technician is responsible for executing routine and critical parenteral drug product manufacturing operations for highly sensitive pharmaceutical and biologic products in a controlled environment.

Salary

Base: $16.70 - $20.24 per hour; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • Parenteral manufacturing equipment operation
  • Aseptic technique and contamination control
  • cGMP and data integrity principles
  • Equipment setup, changeover, and cleaning
  • Sterilization and depyrogenation processes
  • Environmental Health & Safety (EHS) procedures

Nice-to-have

  • Continuous improvement of procedures
  • Support for quality investigations
  • Cross-functional collaboration skills
  • Adaptability to new technologies
  • Training new employees

Key Requirements

  • High school diploma or equivalent
  • Minimum 2 years parenteral/aseptic manufacturing experience
  • 3 years pharmaceutical manufacturing experience
  • Experience with automated/computer-controlled equipment preferred
  • Prior formulation, preparation, or sterile filling experience strongly preferred

Work Rights

Not specified

Tailored Resume

Cover Letter