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

Ferring B.V

Parsippany, New Jersey, United States
Base: $89,000 to $105,000; bonus/equity: annual bo...
Cgmp compliance and regulatory adherence
Process improvement and troubleshooting
Cross-functional team collaboration
As the Process Engineer II, you will optimize and enhance manufacturing processes to achieve the highest quality and efficiency in pharmaceutical production by leveraging your expertise in engineering principles, process design, and regulatory compliance

Job Summary

  • As the Process Engineer II, you will optimize and enhance manufacturing processes to achieve the highest quality and efficiency in pharmaceutical production by leveraging your expertise in engineering principles, process design, and regulatory compliance.
  • Ferring offers competitive total compensation along with an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work.
  • Ferring is an equal opportunity employer committed to a 'People First' philosophy and maintains a drug-free workplace.

Matching Summary

As the Process Engineer II, you will optimize and enhance manufacturing processes to achieve the highest quality and efficiency in pharmaceutical production by leveraging your expertise in engineering principles, process design, and regulatory compliance.

Salary

Base: $89,000 to $105,000; Bonus/Equity: Annual bonus based on individual and company performance; Benefits: Comprehensive healthcare, 401k with match, disability, life insurance, paid time off, parental leave

Skills & Requirements

Must-have

  • cGMP compliance and regulatory adherence
  • Process improvement and troubleshooting
  • Cross-functional team collaboration
  • Aseptic processing and lyophilization expertise
  • Manufacturing process validation support
  • Shift work flexibility including weekends

Nice-to-have

  • Strong customer focus and communication
  • Entrepreneurial and agile work environment
  • Continuous improvement initiatives
  • Hands-on use of analysis and quality software

Key Requirements

  • Bachelor’s degree in mechanical, chemical, or electrical engineering
  • Minimum three years pharmaceutical engineering experience
  • Knowledge of GMP and FDA regulations
  • Experience with aseptic processing and lyophilization
  • Ability to work 1st, 2nd, or 3rd shifts including weekends

Work Rights

Not specified

Tailored Resume

Cover Letter