Senior Process Engineer - (1st/2nd/3rd Shifts)

Ferring

Parsippany, New Jersey, United States
Base: $120,000 to $138,000; shift differential: 10...
Onsite (specific shift not mentioned)
7+ years pharmaceutical gmp experience
Equipment design and commissioning
Iq/oq/pq validation protocols
Ferring is seeking a Senior Process Engineer to provide advanced engineering support for pharmaceutical manufacturing equipment and processes in a cGMP-regulated environment. The role involves leading complex technical projects, ensuring compliance, and collaborating with cross-functional teams while promoting continuous improvement

Job Summary

  • The Senior Process Engineer will lead complex technical projects ensuring compliant and reliable operations in a cGMP-regulated biopharmaceutical environment.
  • This role requires subject matter expertise during audits and inspections while supporting the design, installation, and qualification of new manufacturing equipment.
  • Ferring offers competitive compensation with shift differentials up to 20%, comprehensive healthcare, 401k matching, and a culture recognized as one of the best places to work.

Matching Summary

Match Score: 85

Ferring is seeking a Senior Process Engineer to provide advanced engineering support for pharmaceutical manufacturing equipment and processes in a cGMP-regulated environment. The role involves leading complex technical projects, ensuring compliance, and collaborating with cross-functional teams while promoting continuous improvement.

Salary

Base: $120,000 to $138,000; Shift Differential: 10% for 2nd shift, 20% for 3rd shift; Bonus: Annual incentive compensation based on performance

Skills & Requirements

Must-have

  • 7+ years pharmaceutical GMP experience
  • Equipment design and commissioning
  • IQ/OQ/PQ validation protocols
  • cGMP regulatory compliance
  • PLC programming and troubleshooting
  • Aseptic systems and lyophilizers
  • Risk assessment (FMEA)

Nice-to-have

  • Cross-functional collaboration skills
  • Continuous process improvement mindset
  • Vendor management experience
  • Data integrity expertise
  • Strong analytical problem-solving

Key Requirements

  • Bachelor's degree in Engineering or 12+ years equivalent experience
  • Minimum 7 years in pharmaceutical/biopharma GMP operations
  • Proficiency in automation interfaces and quality systems software
  • Ability to work on-call and off-shifts including weekends/holidays
  • Physical ability to work in cleanrooms and lift 25 lbs

Work Rights

Not specified

Tailored Resume

Cover Letter