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Pharmaceutical Process Engineer Jobs in Iowa (NOW HIRING)

Senior Process Engineer

Charles City, IA

$94K - $121K/yr

The senior engineer oversees multi-step, multi-year programs that define the cGMP manufacturing process for active pharmaceutical ingredients. They are an engineering expert, interfacing with ...

Senior Process Engineer

Charles City, IA · On-site

$94K - $121K/yr

The senior engineer oversees multi-step, multi-year programs that define the cGMP manufacturing process for active pharmaceutical ingredients. They are an engineering expert, interfacing with ...

Senior Process Engineer

Charles City, IA · On-site

$94K - $121K/yr

The senior engineer oversees multi-step, multi-year programs that define the cGMP manufacturing process for active pharmaceutical ingredients. They are an engineering expert, interfacing with ...

Senior Process Engineer

Cedar Rapids, IA · On-site

$102K - $132K/yr

Senior Process Engineer Your Role at BSI Our Process Engineers are responsible for designing safe ... food & beverage, pharmaceutical, and consumer products. We design manufacturing process for ...

Job Overview As a Process Engineer II, you'll build on your chemical engineering experience while ... with pharmaceutical clients worldwide and to work on multiple processes each year. This position ...

Job Overview As a Process Engineer II, you'll build on your chemical engineering experience while ... Experience in a chemical manufacturing environment, particularly pharmaceutical, is preferred.

Overview: As a Process Engineer II, you'll build on your chemical engineering experience while ... with pharmaceutical clients worldwide and to work on multiple processes each year. This position ...

Troubleshooting, investigating process problems and deviations, and preparing appropriate reports ... pharmaceutical manufacture; or equivalent education/experience Employment Type: FULL_TIME

Troubleshooting, investigating process problems and deviations, and preparing appropriate reports ... pharmaceutical manufacture; or equivalent education/experience Employment Type: FULL_TIME

Troubleshooting, investigating process problems and deviations, and preparing appropriate reports ... pharmaceutical manufacture; or equivalent education/experience Cambrex is committed to providing a ...

Troubleshooting, investigating process problems and deviations, and preparing appropriate reports ... pharmaceutical manufacture; or equivalent education/experience Cambrex is committed to providing a ...

Troubleshooting, investigating process problems and deviations, and preparing appropriate reports ... pharmaceutical manufacture; or equivalent education/experience Cambrex is committed to providing a ...

Troubleshooting, investigating process problems and deviations, and preparing appropriate reports ... pharmaceutical manufacture; or equivalent education/experience Cambrex is committed to providing a ...

Education: Ph.D. in Microbiology, Virology, Biochemical Engineering, Chemical Engineering ... Minimum of 2-3 years of experience supporting vaccine, biologics, biotechnology, or pharmaceutical ...

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Pharmaceutical Process Engineer information

See Iowa salary details

$28

$33

$36

How much do pharmaceutical process engineer jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for pharmaceutical process engineer in Iowa is $33.10, according to ZipRecruiter salary data. Most workers in this role earn between $31.15 and $35.00 per hour, depending on experience, location, and employer.

What does a pharmaceutical process engineer do?

A pharmaceutical process engineer reviews the requirement to produce a pharmaceutical product and develops a process for manufacturing. In this career, your duties vary from employer to employer but usually include tasks such as providing technical specifications for machinery and equipment, working to estimate costs for production, and undertaking a negotiation for the procurement of necessary materials and ingredients. Your responsibilities as a process engineer may include providing analysis of the process to ensure efficiency, safety, and compliance with relevant regulations.

What does a pharmaceutical process engineer do?

A Pharmaceutical Process Engineer is responsible for designing, developing, and optimizing processes used in the manufacturing of pharmaceutical products. They ensure that production methods are efficient, safe, and compliant with regulatory standards. Their work involves troubleshooting process problems, implementing new technologies, and collaborating with other departments to improve product quality and production efficiency. They play a critical role in scaling up laboratory processes to full-scale manufacturing while maintaining product integrity and safety.

What are some common challenges faced by pharmaceutical process engineers when scaling up production from laboratory to manufacturing scale?

Pharmaceutical Process Engineers often encounter challenges when translating lab-scale processes to full-scale manufacturing, such as maintaining product quality, ensuring process consistency, and meeting strict regulatory requirements. Controlling variables like temperature, pressure, and mixing at a larger scale can introduce unforeseen issues that require innovative problem-solving. Collaboration with cross-functional teams—including quality assurance, validation, and production staff—is essential to address these challenges efficiently. Adaptability and attention to detail are crucial in ensuring a smooth and compliant scale-up process.

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

To thrive as a Pharmaceutical Process Engineer, you need a strong background in chemical or process engineering, pharmaceutical manufacturing, and regulatory compliance, typically supported by a relevant engineering degree. Familiarity with process simulation software (such as Aspen Plus), GMP standards, and quality management systems is essential. Attention to detail, problem-solving skills, and effective teamwork are crucial soft skills for optimizing processes and ensuring product quality. These competencies are vital for developing efficient, safe, and compliant pharmaceutical manufacturing processes that meet industry standards.

What is the difference between Pharmaceutical Process Engineer vs Pharmaceutical Manufacturing Technician?

AspectPharmaceutical Process EngineerPharmaceutical Manufacturing Technician
Required CredentialsBachelor's degree in engineering, chemistry, or related field; often includes certifications in process validationHigh school diploma or associate degree; on-the-job training or technical certifications
Work EnvironmentDesign, optimize, and oversee manufacturing processes in labs or production facilitiesOperate equipment, monitor production lines, and ensure quality in manufacturing settings
Employer & Industry UsagePharmaceutical companies, biotech firms, contract manufacturing organizationsPharmaceutical manufacturing plants, biotech production facilities

The main difference is that Pharmaceutical Process Engineers focus on designing and improving manufacturing processes, requiring higher technical credentials, while Pharmaceutical Manufacturing Technicians handle day-to-day production tasks and equipment operation. Both roles are essential in pharmaceutical production but differ in responsibilities and qualifications.

What are popular job titles related to Pharmaceutical Process Engineer jobs in Iowa?

For Pharmaceutical Process Engineer jobs in Iowa, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Process Engineer jobs in Iowa look for?

The top searched job categories for Pharmaceutical Process Engineer jobs in Iowa are:

What are popular job titles related to Pharmaceutical Process Engineer jobs in IA?

For Pharmaceutical Process Engineer jobs in IA, the most frequently searched job titles are:

Infographic showing various Pharmaceutical Process Engineer job openings in Iowa as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 17% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $68,857 per year, or $33.1 per hour.

Senior Process Engineer

Charles City, IA


Cambrex
Pharmaceutical and Medicine Manufacturing • 1 - 5K employees

8.1

Company rating: 8.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

38th of 86 rated pharmaceutical

People enjoy working here

Good employer


$94K - $121K/yr

Full-time

Medical, Life, Retirement

Re-posted 28 days ago


Job description

Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,000 professionals servicing global clients. Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.

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:

As an expert in their field, the Senior Process Engineer leads technical teams responsible for the manufacture of active pharmaceutical ingredients. The senior engineer oversees multi-step, multi-year programs that define the cGMP manufacturing process for active pharmaceutical ingredients. They are an engineering expert, interfacing with internal leadership and external clients to solve complex technical problems and ensure high-quality manufacturing. As a Senior Process Engineer, you will serve as a senior member of our engineering team, taking a leading role in advancing the development and manufacture of active pharmaceutical ingredients. Building on your experience, you'll guide large, multi-year projects that bring complex new medicines from the laboratory to full-scale batch manufacturing, while introducing innovative technologies that enhance our operations.

In this role, you'll mentor and develop junior engineers, helping shape the next generation of talent while receiving mentorship yourself to prepare for senior leadership opportunities - whether as a subject-matter expert or within management. As part of a global contract development and manufacturing organization, you'll collaborate with clients worldwide, tackle technical challenges across diverse processes and unit operations, and make a lasting impact on the success of both our company and the patients who depend on our work.

Responsibilities:

Lead multi-step, multi-year technical programs for the development of the manufacturing process for an API from the initial pilot batches to full commercialization.

Oversee the conceptual process design for complete API programs including: scaling calculations for unit operations, equipment selection, production planning, and determination of operating parameters.

Lead process reviews for operability, safety, and quality.

Operate as a subject-matter expert for external clients and internal stakeholders.

Mentor junior engineers and scientists.

Initiate improvements through ideation, process modelling and the analysis of production and laboratory data.

Lead complex quality investigations and corrective action / preventative action implementation.

Identify, oversee, and conduct process improvement projects to reduce cycle time, increase yield, and improve quality.

Coordinate the drafting of manufacturing documents: process flow diagrams, batch records, validation protocols, standard operating procedures, quality investigations, campaign reports.

Optional Additional Responsibility: Lead a team of 2-5 engineers as direct reports, overseeing career development and project assignments.

Qualifications / Skills:
  • Applied Math and Science: A complete understanding of the core chemical engineering fundamentals (thermodynamics, heat transfer, mass transfer, transport, kinetics, etc.) and an intuitive sense for their application to real-world problems.
  • Data Analysis, Visualization, Troubleshooting: The ability to analyze data from various sources, including sensors and experiments, to identify trends, troubleshoot issues, and improve efficiency.
  • Process Simulation and Modeling: Advanced use of software (spreadsheets, programming, simulators) to model chemical unit operations and processes.
  • Process Safety and Risk Management: Instinctively assess and manage risks associated with chemical processes, ensuring the safety of personnel and the environment.
  • Process Scale Up & Equipment knowledge: Assess equipment capability of key processing equipment (reactors, filters, heat exchangers) with respect to process fit. Proposes alternatives that incorporate business objectives and optimize the use of resources.
  • Problem-Solving: Lead discussions and ideation to identify, analyze, and solve complex problems related to chemical processes and plant operations. Includes investigations.
  • Technical Writing & Communication: The ability to explain technical concepts clearly and accurately to technical and non-technical audiences.
  • Attention to Detail: Be meticulous and pay close attention to detail to ensure accuracy and quality. Review documents and the work of others.
  • Adaptability: Adapt to changing priorities, new technologies, and unexpected challenges is important. Assist others with change management.
  • Project Management, Leadership, & Mentoring: Manage one's own assignments, delegate, and support others. Manage projects, including timelines, resources, and budgets. Lead teams and mentor junior engineers. Ensure all projects meet the assigned deadlines.
Education, Experience, and Licensing Requirements: (Text Only)- B.S. degree in Chemical Engineering or related field. - 7-15 years of experience in chemical development, chemical manufacturing, chemical engineering design, or the equivalent. - Experience in a chemical manufacturing environment, particularly pharmaceutical, is preferredEmployment Type: FULL_TIME

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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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Pay

Benefits

Hours and flexibility

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