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Pharmaceutical Process Engineer Jobs (NOW HIRING)

DPS Group

Process Engineer

Framingham, MA · On-site

The Process Engineer will contribute to the creation of design and technical documents to support ... Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic ...

Evonik

Process Engineer

Lafayette, IN

Summary Apply process engineering knowledge and skills to support the synthesis of starting materials pharmaceutical intermediates and final bulk products in a safe, efficient, and environmentally ...

Evonik Industries

Process Engineer

Lafayette, IN · On-site

Summary Apply process engineering knowledge and skills to support the synthesis of starting materials pharmaceutical intermediates and final bulk products in a safe, efficient, and environmentally ...

NCSL International

Process Engineer

Morrisville, NC · On-site

$100 - $125/hr

Process Engineer * Penzberg, Bavaria DE, Germany, 82377 * Full Time About the Job: The Process ... pharmaceutical, engineering, field service, or diagnostic laboratory setting Preferred ...

Actalent

Process Engineer

Saint Louis, MO

Hands-on experience in process engineering within biopharmaceutical or pharmaceutical environments. * Practical experience or strong interest in chromatography, with the ability to perform ...

Augment Professional Services

Process Engineer

Austin, TX · On-site

$100 - $125/hr

Chemical / Process Engineer - Advanced Manufacturing Location / Worksite On-site / Project-Based ... Semiconductor, battery, chemical processing, pharmaceutical, manufacturing, or cleanroom experience.

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Pharmaceutical Process Engineer information

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How much do pharmaceutical process engineer jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for pharmaceutical process engineer in the United States is $35.25, according to ZipRecruiter salary data. Most workers in this role earn between $33.17 and $37.26 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.

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Pharmaceutical Process Engineer jobs near you
Infographic showing various Pharmaceutical Process Engineer job openings in the United States 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 $73,310 per year, or $35.2 per hour.

Process Engineer

Stark Pharma Solutions Inc

Minneapolis, MN • On-site

Contractor

Re-posted 13 days ago

Job description

Hi,

My name is Karthik Mutyala and I’m a Recruitment Manager with Stark Pharma, specializing in pharmaceutical, biotechnology, and medical device roles. I came across your profile and wanted to see if you are open to new opportunities.

If interested, please send me your updated resume along with the best number and time to reach you.

Job Title: Tech Transfer Process Engineer

Location: Minneapolis, MN (Hybrid)

Schedule: Initially 1 week/month onsite, increasing to 50–60% onsite during project execution

Contract Duration: 12+ Months

Position Overview

We are seeking an experienced Tech Transfer Process Engineer to support technology transfer and startup activities within a pharmaceutical/biologics manufacturing environment. This role will focus on process knowledge transfer, operational readiness, startup execution, and CQV support across both upstream and downstream manufacturing systems.

The engineer will join during the late design phase and play a key role in transitioning systems into execution, commissioning, qualification, and startup activities while supporting manufacturing readiness and field operations.

Key Responsibilities

  • Support technology transfer activities for pharmaceutical and biologics manufacturing processes
  • Assist with startup execution, process scale-up, and operational readiness activities
  • Provide technical support across upstream and downstream processing operations
  • Support commissioning, qualification, and validation (CQV) activities for manufacturing systems and equipment
  • Collaborate with Engineering, Manufacturing, Validation, and Operations teams during project execution
  • Support CIP (Clean-in-Place) systems and related process integration activities
  • Assist with troubleshooting, process optimization, and startup issue resolution
  • Participate in field execution activities and support early construction ramp-up efforts
  • Ensure documentation and activities align with GMP and regulatory expectations

Required Qualifications

  • 5+ years of experience as a Tech Transfer Process Engineer within pharmaceutical or biologics manufacturing environments
  • Hands-on experience supporting startup and technology transfer activities
  • Strong understanding of upstream and downstream bioprocessing operations
  • Experience supporting CQV (Commissioning, Qualification, and Validation) activities
  • Working knowledge of CIP (Clean-in-Place) systems
  • Strong cross-functional communication and collaboration skills