Inspection & Packaging Operator I

Bristol Myers Squibb

Manati, PR, US
Base: $10.63 - $12.88 ph; bonus/equity: + incentiv...
Hybrid (50% onsite)
Operating automatic and semi-automatic inspection equipment
Manual and semi-automated packaging of liquid and lyophilized products
Knowledge of good manufacturing practices (cgmp)
Bristol Myers Squibb is seeking an Inspection & Packaging Operator I for their facility in Manati, PR. The role involves ensuring compliance with Good Manufacturing Practices while performing inspection and packaging tasks, with a focus on quality and accuracy

Job Summary

  • This role involves performing the inspection and packaging of finished goods in accordance with Good Manufacturing Practices and safety regulations.
  • Employees will operate both automatic and semi-automatic equipment to minimize downtime while ensuring high-quality output for syringes and combination products.
  • Bristol Myers Squibb offers competitive benefits including health coverage, 401(k) plans, and paid time off to support employee wellbeing.

Matching Summary

Match Score: 75

Bristol Myers Squibb is seeking an Inspection & Packaging Operator I for their facility in Manati, PR. The role involves ensuring compliance with Good Manufacturing Practices while performing inspection and packaging tasks, with a focus on quality and accuracy.

Salary

Base: $10.63 - $12.88 per hour; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Medical, dental, vision, 401(k), paid time off, and wellness programs included

Skills & Requirements

Must-have

  • Operating automatic and semi-automatic inspection equipment
  • Manual and semi-automated packaging of liquid and lyophilized products
  • Knowledge of Good Manufacturing Practices (cGMP)
  • Accurate visual inspection of product defects
  • Completing error-free electronic and manual documentation
  • Cleaning packaging lines according to procedures

Nice-to-have

  • Ability to operate pallet jacks
  • Willingness to work irregular hours and rotative shifts
  • Participation in special projects and audits
  • Good communication and interpersonal skills
  • Basic knowledge on computerized systems

Key Requirements

  • High School Diploma
  • At least one year of experience within pharmaceutical industry
  • Knowledge of cGMP practices and EHS regulations

Work Rights

Not specified

Tailored Resume

Cover Letter