Sterile Specialist, Engineering (onsite)

Our Company

Rahway, NJ, USA
Base: $87,300.00 - $137,400.00; bonus/equity: elig...
Hybrid
Sterile drug product manufacturing equipment
Cgmp and safety requirements
Equipment troubleshooting and routine interaction
This Engineer position will provide on-site engineering support of the Rahway, NJ FLEx (Formulation, Laboratory & Experimentation) center, for sterile operations within Our Company's Research Labs Pharmaceutical Sciences (Pharm Sci), Pharmaceutical Operations Engineering group (Pharm Ops Engineering)

Job Summary

  • This Engineer position will provide on-site engineering support of the Rahway, NJ FLEx (Formulation, Laboratory & Experimentation) center, for sterile operations within Our Company's Research Labs Pharmaceutical Sciences (Pharm Sci), Pharmaceutical Operations Engineering group (Pharm Ops Engineering).
  • The primary responsibility of this role is to maintain 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 salary range for this role is $87,300.00 - $137,400.00 and the successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

Matching Summary

This Engineer position will provide on-site engineering support of the Rahway, NJ FLEx (Formulation, Laboratory & Experimentation) center, for sterile operations within Our Company's Research Labs Pharmaceutical Sciences (Pharm Sci), Pharmaceutical Operations Engineering group (Pharm Ops Engineering).

Salary

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

Skills & Requirements

Must-have

  • Sterile Drug Product manufacturing equipment
  • cGMP and Safety requirements
  • Equipment troubleshooting and routine interaction
  • Sterilization and cleaning validation
  • GMP documentation maintenance

Nice-to-have

  • Independent problem-solving ability
  • Effective organizational skills
  • Adaptability to business flow
  • Strong computer skills

Key Requirements

  • Bachelor's degree in engineering or science
  • Minimum 2 years of related Drug Product/Sterile/Validation experience
  • Familiarity with Quality, cGMP, Safety & Environmental Policies
  • Troubleshooting ability (mechanical/electrical/automation)

Work Rights

Not specified

Tailored Resume

Cover Letter