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Synerfac Technical Staffing

Process Engineer I

Entry-Level JobVerifiedNo experience needed

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What they do

A Process Engineer solves problems related to the manufacturing and use of products, including chemicals, fuel, food, and clothing. Designs new products, improves existing ones, or develops new processes for better use of existing materials. May specialize in a chemical engineering process, such as making plastics, or in an industry such as health care.

$109,039 / year median in New Jersey

+3% projected growth

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Job Description

Process Engineer I Synerfac Technical Staffing - 3.6 Gibbstown, NJ Job Details $23.00 - $26.50 an hour 5 days ago Qualifications Bachelor's degree in mechanical engineering Biotechnology Chemical engineering unit operations Operational analysis Content creation for technical audiences Quality records maintenance Defect resolution root cause analysis Chemical Engineering Procedural guides Technical documentation Pharmaceutical regulatory compliance Defect analysis Mechanical Engineering Technical writing experience within manufacturing Production deviation management Engineering process optimization Process improvement Equipment troubleshooting Corrective and preventive actions (CAPA) Chemical scale-up projects Manufacturing standard operating procedures Manufacturing facility experience Policy & process development Bachelor's degree in engineering Production validation processes Pharmaceutical company experience Technology transfer (scale-up process) Compliance documentation Incident Investigation Quality control problem-solving Full Job Description Entry-Level Process Engineer-Pharmaceutical Manufacturing 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 Must be available to work Rotating Shifts; 6am to 6pm and 6pm to 6am, including working every other weekend 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 Call to action: If you would like to gain experience in GMP manufacturing and want a hands-on role supporting pharmaceutical production in a high-compliance environment, apply today.
Disclaimer:
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