Sterile Specialist, Engineering (onsite)

med-in.at

Rahway, NJ, US
Base: $87,300.00 - $137,400.00; bonus/equity: elig...
Hybrid
Sterile drug product manufacturing equipment
Gmp and safety compliance
Equipment troubleshooting mechanical electrical automation
This Engineer position will provide on-site engineering support of the Rahway, NJ FLEx center for sterile operations within the Pharmaceutical Sciences and Pharmaceutical Operations Engineering groups

Job Summary

  • This Engineer position will provide on-site engineering support of the Rahway, NJ FLEx center for sterile operations within the Pharmaceutical Sciences and Pharmaceutical Operations Engineering groups.
  • The role includes maintaining facility, utilities, and manufacturing equipment in accordance with GMP and Safety requirements while applying Reliability Maintenance best practices to ensure timely availability of clinical and development batches.
  • The successful candidate will be eligible for annual bonus and long-term incentive and offered a comprehensive benefits package including medical, dental, vision, retirement benefits, paid holidays, vacation, and sick days.

Matching Summary

This Engineer position will provide on-site engineering support of the Rahway, NJ FLEx center for sterile operations within the Pharmaceutical Sciences and Pharmaceutical Operations Engineering groups.

Salary

Base: $87,300.00 - $137,400.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Medical, dental, vision, retirement, paid holidays, vacation, and sick days

Skills & Requirements

Must-have

  • Sterile Drug Product manufacturing equipment
  • GMP and Safety compliance
  • Equipment troubleshooting mechanical electrical automation
  • Computerized Maintenance Management Systems (CMMS)
  • Quality Engineering support
  • Capital project management
  • Equipment validation lifecycle

Nice-to-have

  • Independent problem-solving
  • Effective communication and technical writing
  • Organizational skills
  • SAP Plant Maintenance experience
  • Paperless electronic validation system
  • Computerized Calibration Maintenance System
  • Planning and Scheduling practices

Key Requirements

  • Bachelor's degree in engineering or science
  • Minimum 2 years related Drug Product/Sterile/Validation experience
  • Familiarity with cGMP and Quality policies
  • Ability to work 2nd shift
  • US and Puerto Rico residents only

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter