Sterile Specialist, Engineering (onsite)

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Rahway, New Jersey, USA
Base: $87,300.00 - $137,400.00; bonus/equity: annu...
Hybrid
Cgmp and safety requirements
Reliability maintenance best practices
Gmp documentation
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; The successful candidate will be eligible for annual bonus and long-term incentive, if applicable; We offer a comprehensive package of benefits.

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: Annual bonus and long-term incentive, if applicable; Benefits: Medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days

Skills & Requirements

Must-have

  • cGMP and Safety requirements
  • Reliability Maintenance best practices
  • GMP documentation
  • sterile validation program
  • sterilization and cleaning validation

Nice-to-have

  • Independent problem-solving
  • SAP Plant Maintenance experience
  • Planning and Scheduling practices

Key Requirements

  • Bachelor's degree in engineering or science
  • 2 years of related Drug Product/Sterile/Validation experience
  • Strong familiarity with Quality, cGMP, Safety & Environmental Policies
  • Familiarity with Sterile Drug Product manufacturing equipment
  • Familiarity with Computerized Maintenance and Management Systems (CMMS)

Work Rights

Not specified

Tailored Resume

Cover Letter