$80,000–$100,000 Per Year
Join a specialized Central New Jersey engineering firm delivering cutting-edge solutions to the pharmaceutical industry. Contribute to high-impact projects designing GMP-compliant processes and equipment for drug substance and product manufacturing.
Key Responsibilities:
Develop conceptual, preliminary, and detailed design packages for process equipment and unit operations
Create and review Process Flow Diagrams (PFDs), Piping & Instrumentation Diagrams (P&IDs), and layout drawings
Support equipment sizing, specification, and process integration of unit operations
Assist with commissioning, qualification protocol development, and execution (CQV)
Required Skills & Experience:
Bachelor"s degree in engineering with 3-5 years of experience in pharmaceutical or biopharmaceutical process engineering
Strong interpersonal skills and ability to work effectively on cross-functional project teams
Self-directed with strong problem-solving skills and ability to manage multiple tasks
Excellent written and verbal communication skills
Preferred Skills & Experience:
Experience developing User Requirement Specifications (URS) and Design Basis documentation
Familiarity with GMP-compliant process design and pharmaceutical manufacturing equipment
Compensation: $80,000-$100,000
Call to Action:
Ready to advance your career in pharmaceutical process engineering? Apply today!
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Anthony Borbely
aborbely@synerfac.com
Synerfac Technical Staffing
732-271-9333S
Synerfac Technical Staffing