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Pharmaceutical Process Engineer Jobs (NOW HIRING)

Stark Pharma Solutions Inc

Senior Process Engineer

Bend, OR · On-site

$109K - $141K/yr

The ideal candidate will have extensive experience in pharmaceutical process design, OSD ... Lead process engineering activities for pharmaceutical and API manufacturing projects. * Review ...

Quality Agents, LLC

Process Engineer

Rockville, MD · On-site

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. We are seeking a detail-oriented and collaborative Process Engineer to support ...

Quality Agents

Process Engineer

Rockville, MD · On-site

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. We are seeking a detail-oriented and collaborative Process Engineer to support ...

Quality Agents, LLC

Process Engineer

Rockville, MD · On-site

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. We are seeking a detail-oriented and collaborative Process Engineer to support ...

Perrigo Company plc

Process Engineer

Bronx, NY · On-site

$95K - $120K/yr

Bachelor's degree in Pharmaceutical Sciences, Chemical Engineering, Pharmaceutical Engineering, Chemistry, or a related scientific discipline. * 2-5 years of pharmaceutical manufacturing, process ...

Visium Resources, Inc.

Be Seen First

Senior Process Engineer

Kankakee, IL · On-site

$140K - $170K/yr

Summary Client is seeking an experienced Senior Process Engineer to support a major pharmaceutical capital expansion project at manufacturing campus in Kankakee, Illinois. Serving as the Owner ...

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Pharmaceutical Process Engineer information

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How much do pharmaceutical process engineer jobs pay per hour?

As of Jul 27, 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 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 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 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 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 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.
More about Pharmaceutical Process Engineer jobs
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Pharmaceutical Process Engineer jobs near you
Infographic showing various Pharmaceutical Process Engineer job openings in the United States as of July 2026, with employment types broken down into 96% Full Time, 1% Part Time, and 3% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $73,310 per year, or $35.2 per hour.
Process Engineer II (Pharmaceutical Manufacturing)

Process Engineer II (Pharmaceutical Manufacturing)

Astrix Inc

Wilmington, OH • On-site

Full-time

Posted 5 days ago

Job description

Pay Rate Low: 90000 | Pay Rate High: 115000
Our client is a global biopharmaceutical company seeking a ProcessEngineer II to support commercial and clinical pharmaceutical manuacturing, with a focus on oral solid dosage (OSD) products.
Title: Process Engineer II (Pharmaceutical Manufacturing)
Salary: $90-115K +Bonus
Hours: 1st shift ~8am-5pm M-F
Location: Onsite in Wilmington, OH (Excellent Relocation assistance provided if needed!)
Summary
The Process Engineer supports commercial and clinical pharmaceutical manufacturing, with a focus on oral solid dosage (OSD) products. This role is responsible for process scaleup and transfer, equipment selection and commissioning, and continuous improvement of manufacturing and packaging operations.
Essential Functions
  • Troubleshoot and maintain manufacturing systems, processes, and equipment.
  • Support the development or transfer of manufacturing and cleaning processes for the manufacturing area.
  • "Hands-on" ability to install and troubleshoot instrumentation and equipment.
  • Author high-quality technical protocols/reports (engineering studies, summary reports, equipment specifications, change controls, and investigations)
  • Specify and size manufacturing systems, equipment, and process equipment.

Basic Qualifications:
  • BS degree in Engineering or technical discipline.
  • 2-5 year of manufacturing experience or technical experience.

Preferred Qualification:
  • 2-5 years of OSD pharmaceutical experience or 5 years of pharmaceutical engineering experience.
  • Experience with OSD equipment procurement.
  • Thorough knowledge of cGMP, OSHA, EPA and FDA facility requirements and regulations.
  • Thorough knowledge of OSD operations, statistics, equipment design, process control, and process scale-up.
  • Knowledge of OSD pharmaceutical process and equipment validations.
  • Experience in statistical analysis: sample sizing, ANOVA, regression analysis, control charts, etc
  • MUST be authorized to work in the US without sponsorship

Physical Demands
  • Ability to properly gown and don PAPR for potent controlled substance formulations for extended periods of time
  • Ability to lift/move 40 lbs. overhead. Ability to team lift up to 100 lbs.
  • Must be able to be medically cleared for respirator use (PAPR)
  • Ability to operate different types of production equipment.
  • Ability to gown correctly for clean room manufacturing operations.
  • Ability to stand or sit for extended periods (up to 2 hours at a time).
  • Must be able to work in an office and a manufacturing environment.

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