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Contract Process Engineer Jobs in New Jersey (NOW HIRING)

Hutchinson Industries Inc

Process Engineer

Trenton, NJ · On-site

$70K - $90K/yr

Process Engineer General Description Responsible for evaluating existing processes and configuring ... Neither this nor any other communication creates an employment contract between Hutchinson ...

Axens North America

Process Engineer I

Princeton, NJ · On-site

$77K - $83K/yr

Job Summary The Process Engineer I is mainly participating and assisting in the preparation of the deliverables of the Process Design Packages in the frame of Licensing contracts, on the specific ...

Kiewit

Supply Chain/Contracts Specialist

Woodcliff Lake, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Own and manage the contract process for assigned materials/equipment. Negotiate T's and C's on the ... Interface with Engineering and/or construction teams to provide insight about status of cost ...

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All JobsContract Process Engineer JobsContract Process Engineer Jobs in New Jersey

Contract Process Engineer information

See New Jersey salary details

$50.3K

$93.4K

$144.7K

How much do contract process engineer jobs pay per year?

As of Aug 19, 2026, the average yearly pay for contract process engineer in New Jersey is $93,420.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,600.00 and $104,600.00 per year, depending on experience, location, and employer.

What is a contract process engineer?

Contract Process Engineers are professionals who are hired on a temporary or project-specific basis to design, optimize, and troubleshoot industrial processes within a company. They often work in industries such as chemicals, pharmaceuticals, oil and gas, or manufacturing, providing technical expertise to improve production efficiency, safety, and quality. Their responsibilities may include process design, equipment specification, project management, and ensuring regulatory compliance. Because they work on a contract basis, their assignments may vary in length and scope depending on the needs of the employer.

What types of projects or industries do contract process engineers typically work on, and how does this influence their daily responsibilities?

Contract Process Engineers often work on short- to medium-term assignments across industries such as pharmaceuticals, chemicals, oil and gas, and manufacturing. The nature of their projects can range from process optimization and troubleshooting to equipment commissioning and plant upgrades. Depending on the industry and project scope, daily responsibilities may include conducting process simulations, collaborating with multidisciplinary teams, preparing technical documentation, and ensuring compliance with safety and quality standards. This variety allows for broad experience, but also requires adaptability and strong communication skills to integrate quickly with new teams and workflows.

What are the key skills and qualifications needed to thrive as a contract process engineer, and why are they important?

To thrive as a Contract Process Engineer, you need a solid background in chemical or process engineering, experience with process optimization, and a relevant engineering degree. Familiarity with process simulation software (like Aspen HYSYS or CHEMCAD), project management tools, and safety compliance standards is typically expected. Strong analytical thinking, effective communication, and adaptability are valuable soft skills for managing changing project requirements and collaborating with diverse teams. These skills ensure efficient, safe, and cost-effective process improvements that meet contractual obligations and client expectations.

What is the difference between Contract Process Engineer vs Process Engineer?

AspectContract Process EngineerProcess Engineer
CredentialsBachelor's in Engineering, relevant certifications (e.g., Six Sigma)Bachelor's or higher in Engineering, similar certifications
Work EnvironmentContract-based, project-specific, often in industrial or manufacturing settingsFull-time, ongoing roles in manufacturing, chemical, or industrial plants
Employer & Industry UsageUsed by companies hiring temporary or project-based engineersEmployed by companies for continuous process improvement and operations
Search & Comparison IntentCommonly compared for project-based roles and contract workCompared for permanent roles in process optimization

The Contract Process Engineer typically works on temporary, project-specific assignments, focusing on process improvements within a set timeframe. In contrast, the Process Engineer holds a permanent position, overseeing ongoing operations and continuous process optimization. Both roles require similar qualifications but differ mainly in employment type and work scope.

What are the most commonly searched types of Process Engineer jobs in New Jersey?

The most popular types of Process Engineer jobs in New Jersey are:

What are popular job titles related to Contract Process Engineer jobs in New Jersey?

For Contract Process Engineer jobs in New Jersey, the most frequently searched job titles are:

What job categories do people searching Contract Process Engineer jobs in New Jersey look for?

The top searched job categories for Contract Process Engineer jobs in New Jersey are:

What cities in New Jersey are hiring for Contract Process Engineer jobs?

Cities in New Jersey with the most Contract Process Engineer job openings:

Contract Process Engineer jobs near you
Infographic showing various Contract Process Engineer job openings in New Jersey as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $93,420 per year, or $44.9 per hour.

Process Engineer

Katalyst Healthcares and Lifesciences

Morristown, NJ • On-site

Other

Posted 4 days ago

Job description

Responsibilities:
  • Provide technical support for all products manufactured externally at third party contract manufacturers, North American locations. Frequent visits to third party sites for batch monitoring are required.
  • ct as the technical expert on all product formulations, scale-up activity, process validation, equipment qualification, process related technical issues and investigations to ensure sites adhere to GMP and regulatory guidelines.
  • Review and/or author technical protocols, reports or memos.
  • Lead Continued Process Verification (CPV) activities across Contract Manufacturing Organizations (CMOs).
  • This includes overseeing data collection and analysis, ensuring ongoing process performance and control, partnering with CMOs to identify and mitigate risks, and driving continuous improvements to strengthen product robustness.
  • The role will collaborate closely with Quality, MSAT, and CMO technical teams to ensure compliance with regulatory expectations and maintain a state of control throughout the product lifecycle.
  • Support manufacturing tech transfer of new and existing products.
  • Support multi-functional teams to formulate plans and strategy that meet defined objectives.
  • Troubleshoot manufacturing issues, conduct effective problem-solving and provide solutions leading to product releases.
  • Review, execute and support validation activities at third party contractors.
  • Work with Regulatory teams as needed to support product submissions to the FDA.
Requirements:
  • Bachelor of Science, Pharmacy, Engineering, or Chemistry.
  • 8 to 10+ years in Pharmaceutical Operations or Technical Operations with the application of cGMPs in the Pharmaceutical or related regulated industry.
  • 10+ years in a Technical Services or engineering function.
  • Experience in third party manufacturing, technical services support function and plant operations.
  • Good knowledge and hands-on application of Word, Excel, and Powerpoint are necessary.
Skills:
  • Thorough knowledge of cGMP's and regulatory requirements with respect to development, engineering and validation of pharma products.
  • Comprehensive knowledge of drug product manufacturing for solid and liquid oral dosages. Knowledge of API manufacturing a plus.
  • bility to work in cross functional teams, provide strong analytical skills for troubleshooting and root cause analysis, and communicate with internal and external team members.
  • Knowledge of product manufacture, formulation, quality, FDA and EMA regulations, technical transfer, process development and validation.
  • Skilled in improving productivity, cost analysis, and plant equipment evaluation.

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