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Contract Validation Engineer Jobs in Iowa (NOW HIRING)

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... Work with Validation Engineering and Maintenance departments on developing and maintaining IQ, OQ ...

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... Work with Validation Engineering and Maintenance departments on developing and maintaining IQ, OQ ...

Contract Duration: 3 months with extension to 12 months with high potential for contract to hire ... Conduct mechanical / electric performance test plans for verification and validation purposes per ...

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... Work with Validation Engineering and Maintenance departments on developing and maintaining IQ, OQ ...

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... Work with Validation Engineering and Maintenance departments on developing and maintaining IQ, OQ ...

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... Work with Validation Engineering and Maintenance departments on developing and maintaining IQ, OQ ...

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... Work with Validation Engineering and Maintenance departments on developing and maintaining IQ, OQ ...

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... Work with Validation Engineering and Maintenance departments on developing and maintaining IQ, OQ ...

Sr. Project Engineer

Denison, IA · On-site

$100K - $120K/yr

Review technical documents and validate field installations, including as-built drawings. * Define ... Manage budgets and assist with contract administration to meet financial targets. Qualifications:

Manufacturing Engineer II

Dubuque, IA

$68K - $88K/yr

Develop engineering solutions and coordinate feasibility testing and validation. * Develop, apply ... Knowledge of project management, contract management, costing, or budgeting. * Strong continuous ...

Manufacturing Engineer

Dubuque, IA · On-site

$68K - $88K/yr

... validation Support the development, application, and evaluation of engineering standards and ... contract management plans Support product development and engineering activities by analyzing ...

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Showing results 1-20

Contract Validation Engineer information

See Iowa salary details

$21

$48

$73

How much do contract validation engineer jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for contract validation engineer in Iowa is $48.84, according to ZipRecruiter salary data. Most workers in this role earn between $37.02 and $59.38 per hour, depending on experience, location, and employer.

What is a contract validation engineer?

A Contract Validation Engineer is responsible for ensuring that systems, processes, and products meet regulatory and contractual requirements. They typically work on a temporary or project basis, verifying compliance through testing, documentation, and analysis. Their role involves collaborating with engineering teams to validate designs, troubleshoot issues, and ensure quality standards are met. This position is common in industries like pharmaceuticals, aerospace, and manufacturing, where strict validation protocols are required.

What are the primary responsibilities of a contract validation engineer on a typical project?

A Contract Validation Engineer is primarily responsible for reviewing and verifying that project deliverables, processes, and products comply with contractual requirements and industry standards. This includes conducting thorough documentation reviews, performing technical validations, and collaborating with project managers, legal teams, and quality assurance professionals to resolve any discrepancies. You will also support audits, maintain compliance records, and participate in meetings to ensure all stakeholders remain informed and aligned. The role often involves both independent analysis and teamwork, providing an excellent environment for those who enjoy balancing technical expertise with cross-functional collaboration.

What are the key skills and qualifications needed to thrive in the contract validation engineer position, and why are they important?

To thrive as a Contract Validation Engineer, you need strong analytical skills, a degree in engineering or a related field, and a deep understanding of contract requirements and industry regulations. Proficiency with validation software, quality management systems (QMS), and relevant certifications such as Six Sigma or ISO standards is often preferred. Outstanding attention to detail, effective communication, and the ability to work collaboratively across departments are crucial soft skills. These competencies ensure accurate contract assessments, regulatory compliance, and seamless integration of contractual obligations into engineering projects.

What are the most commonly searched types of Validation Engineer jobs in Iowa?

The most popular types of Validation Engineer jobs in Iowa are:

What are popular job titles related to Contract Validation Engineer jobs in Iowa?

For Contract Validation Engineer jobs in Iowa, the most frequently searched job titles are:

What job categories do people searching Contract Validation Engineer jobs in Iowa look for?

The top searched job categories for Contract Validation Engineer jobs in Iowa are:

What cities in Iowa are hiring for Contract Validation Engineer jobs?

Cities in Iowa with the most Contract Validation Engineer job openings:

Infographic showing various Contract Validation Engineer job openings in Iowa as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $101,584 per year, or $48.8 per hour.

Production Engineer

Cambrex

Charles City, IA

Full-time

Medical, Life, Retirement

Re-posted 19 days ago


Cambrex rating

8.1

Company rating: 8.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

40th of 86 rated pharmaceutical


Job description

Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. 

With over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and highly potent APIs.

Your Work Matters.

At Cambrex, we strive to build a culture where all colleagues have the opportunity to:

  • engage in work that matters to our customers and the patients they serve
  • learn new skills and enjoy new experiences in an engaging and safe environment
  • strengthen connections with coworkers and the community

We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company.  We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more!

Your Future Matters.

Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!

Overview:

The Production Engineer will be a Operations technical expert and responsible for reviewing documentation for Operations to implement projects for the manufacture of APIs, bulk intermediates, and other products from development through piloting and/or commercial production.

Responsibilities:
  • Writing batch records and cleaning records for commercial products or simple revisions, campaign reports, as needed to support production operations.
  • Initiate SOPs and investigations/deviation reports/CAPAs for production operations and commercial products.
  • Reviewing and approving documentation (batch records, cleaning records, supplements, etc) for Operations as the area technical expert.
  • Troubleshoot equipment and coordinate with maintenance to monitor equipment for efficiency improvement.
  • Assist Process Engineers and Chemical Development teams when new processes are transferred into the area workcenter.
  • Work with Validation Engineering and Maintenance departments on developing and maintaining IQ, OQ and PQ documents and protocols. Ownership of equipment and facility change controls in their assigned area workcenter.
  • Generate product setups and cleaning memos as needed.
  • Troubleshooting, investigating process problems and deviations, and preparing appropriate reports on findings.
  • Participating in HAZOPs and providing guidance on corrective actions when needed.
  • Completing CAPAs and audit action items as assigned.
  • Train Operators or Technicians on equipment and process operations as needed to ensure safe and efficient manufacturing.
  • Additional job duties as assigned.

All employees are required to adhere to DEA, EPA, FDA and cGMP regulations as they relate to the operation of the Company; and to adhere to all company safety rules and procedures. All employees are expected to report to work regularly and promptly. Other duties relating to departmental mission, not specifically detailed in this section may be assigned.

Qualifications / Skills:
  • Knowledge of and/or direct experience in a cGMP environment is preferred
  • General knowledge of chemical operations equipment and manufacturing operations
Education, Experience, and Licensing Requirements: (Text Only)- BS in Chemical Engineering or similar field, plus 1 - 3 years of experience in manufacturing environment, preferably in pharmaceutical manufacture; or equivalent education/experience  Employment Type: FULL_TIME

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Benefits

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About Cambrex

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

East Rutherford, NJ, US

Year founded

1981

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