Chemical Process Engineer

Synerfac Technical Staffing; West Deptford Township (NJ); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Structured onboarding and mentorship

Hands-on experience in pharmaceutical production

Clear career progression opportunities

Job summary

Synerfac Technical Staffing is seeking an Entry-Level Process Engineer in West Deptford Township, NJ, to support pharmaceutical production operations. Ideal candidates should have a Bachelor's degree in Chemical or Mechanical Engineering, with strong problem-solving and communication skills. This role offers hands-on experience in GMP-regulated environments, involving tasks like process optimization and collaboration with manufacturing teams. This is a great opportunity for recent graduates looking to grow in pharmaceutical manufacturing.

Qualifications

• Recent graduates strongly encouraged to apply.
• Internship or academic project experience in regulated environments is preferred.
• Ability to work in a manufacturing/plant environment.

Responsibilities

• Support daily pharmaceutical production operations including batch processing.
• Assist with process optimization and yield improvement.
• Collaborate with cross-functional teams.

Skills

Problem-solving

Communication

Process engineering principles

Education

Bachelor's degree in Chemical Engineering or Mechanical Engineering

Job description

Entry-Level Process Engineer – Pharmaceutical Manufacturing

About the Role

We are seeking a highly motivated recent Chemical or Mechanical Engineering graduate to join a pharmaceutical manufacturing operations in a Production Technician role. This is an entry-level role designed to provide hands‑on exposure to drug substance and drug product manufacturing, equipment, and GMP-regulated processes in a production environment.

Key Responsibilities

• Support daily pharmaceutical production operations, including batch processing, equipment utilization, and troubleshooting
• Assist with process optimization, yield improvement, and cycle time reduction
• Participate in technology transfer, scale‑up, and validation activities
• Support deviation investigations, root cause analysis, and CAPA development
• Author and revise technical documentation including SOPs, batch records, and validation protocols
• Collaborate cross‑functionally with Manufacturing, Quality, Maintenance, and EHS teams
• Ensure all activities comply with cGMP, FDA, and regulatory requirements

Required Qualifications

• Bachelor’s degree in Chemical Engineering, Mechanical Engineering, or related discipline
• 0–2 years of experience (recent graduates strongly encouraged to apply)
• Internship, co‑op, or academic project experience in pharmaceutical, biotech, chemical, or regulated manufacturing preferred
• Fundamental understanding of process engineering principles
• Strong problem‑solving and communication skills
• Ability to work in a manufacturing / plant environment

Preferred Experience

• Exposure to GMP environments
• Familiarity with batch processing, unit operations, or production equipment
• Interest in long‑term career growth within pharmaceutical manufacturing

Why Join Us

• Structured onboarding and mentorship for early‑career engineers
• Hands‑on exposure to commercial pharmaceutical production
• Clear career progression within Manufacturing, MS&T, or Process Engine