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Pharmaceutical Process Engineer Jobs (NOW HIRING)

Tech Tammina LLC

Process Engineer

Palm Beach, FL · On-site

Minimum 5 years of process engineering/project engineering experience in a cGMP, Pharmaceuticals, Biological manufacturing environment. Must have the ability to apply engineering theory, practices ...

Exyte

Senior Process Engineer

Raleigh, NC · On-site

$150 - $200/hr

Ensure designs meet pharmaceutical regulatory requirements, including cGMP, FDA, EMA, and ICH guidelines. * Client Interface: Act as the primary process engineering contact for clients, providing ...

GMP Pros®

Process Engineer

Lincoln, NE · On-site

APPLICANTS MUST HAVE PRIOR EXPERIENCE IN BIOTECH, PHARMACEUTICAL, OR ANIMAL HEALTH INDUSTRIES TO BE CONSIDERED Essential Duties: * Provide process engineering support across production processes.

Clayco (LJC)

Process Engineer

Greenville, SC · On-site

The Process Engineer works closely with clients, process architects, utilities engineers ... Active pharmaceutical ingredients (API) * Oral solid dosage (OSD) * Exposure to additional ...

Clayco (LJC)

Process Engineer

Greenville, SC · On-site

The Process Engineer works closely with clients, process architects, utilities engineers ... Active pharmaceutical ingredients (API) * Oral solid dosage (OSD) * Exposure to additional ...

Exyte Group

Senior Process Engineer

Raleigh, NC · On-site

$132K/yr

Ensure designs meet pharmaceutical regulatory requirements, including cGMP, FDA, EMA, and ICH guidelines. * Client Interface: Act as the primary process engineering contact for clients, providing ...

Clayco (LJC)

Process Engineer

Chicago, IL · On-site

The Process Engineer works closely with clients, process architects, utilities engineers ... Active pharmaceutical ingredients (API) * Oral solid dosage (OSD) * Exposure to additional ...

Clayco

Process Engineer

Chicago, IL · On-site

$135K - $185K/yr

The Process Engineer works closely with clients, process architects, utilities engineers ... Active pharmaceutical ingredients (API) * Oral solid dosage (OSD) * Exposure to additional ...

Clayco (LJC)

Process Engineer

Greenville, SC · On-site

The Process Engineer works closely with clients, process architects, utilities engineers ... Active pharmaceutical ingredients (API) * Oral solid dosage (OSD) * Exposure to additional ...

Clayco (LJC)

Process Engineer

Chicago, IL · On-site

The Process Engineer works closely with clients, process architects, utilities engineers ... Active pharmaceutical ingredients (API) * Oral solid dosage (OSD) * Exposure to additional ...

Clayco (LJC)

Process Engineer

Chicago, IL · On-site

The Process Engineer works closely with clients, process architects, utilities engineers ... Active pharmaceutical ingredients (API) * Oral solid dosage (OSD) * Exposure to additional ...

Augment Professional Services

Process Engineer

Austin, TX · On-site

$60 - $95/hr

Semiconductor, battery, chemical processing, pharmaceutical, manufacturing, or cleanroom experience ... engineering delivery, and industrial construction. Through a flexible services model that includes ...

Clayco

Process Engineer

Greenville, SC · On-site

The Process Engineer works closely with clients, process architects, utilities engineers ... Active pharmaceutical ingredients (API) * Oral solid dosage (OSD) * Exposure to additional ...

Clayco (LJC)

Process Engineer

Chicago, IL

The Process Engineer works closely with clients, process architects, utilities engineers ... Active pharmaceutical ingredients (API) * Oral solid dosage (OSD) * Exposure to additional ...

Clayco (LJC)

Process Engineer

Greenville, SC · On-site

The Process Engineer works closely with clients, process architects, utilities engineers ... Active pharmaceutical ingredients (API) * Oral solid dosage (OSD) * Exposure to additional ...

Clayco (LJC)

Process Engineer

Greenville, SC · On-site

The Process Engineer works closely with clients, process architects, utilities engineers ... Active pharmaceutical ingredients (API) * Oral solid dosage (OSD) * Exposure to additional ...

Clayco (LJC)

Process Engineer

Chicago, IL · On-site

The Process Engineer works closely with clients, process architects, utilities engineers ... Active pharmaceutical ingredients (API) * Oral solid dosage (OSD) * Exposure to additional ...

Salas O'Brien

Process Engineer

Raleigh, NC · On-site

Process Engineer At Salas O'Brien we tell our clients that we're engineered for impact. This ... This role will primarily support pharmaceutical, biotech, and life sciences clients, as well as ...

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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

Tech Tammina LLC

Palm Beach, FL • On-site

Full-time

Re-posted yesterday

Job description

Position: Sr. Process Engineer
Location: United States, , Palm Beach County
Status: Full Time, Permanent
Category: Engineering
 
Overview:
Develop and establish maintenance/engineering tools/programs to ensure that the facility is kept in a good state of repairs as well as all process equipment are cGMP compliant from a facility, maintenance and engineering perspective.
Direct, evaluate and assist capital engineering and process improvement projects.
Facilitate requisitions or equipment and parts.
Serve as equipment/facility expert and interface with regulatory agencies on audits etc.
Develop efficient PM plans for all key pieces of manufacturing equipment etc. and provide troubleshooting expertise in all areas of plant operations and maintenance.
Assist in and or champion investigation of deviations that are facilities/maintenance related, Train SMEs in problem solving techniques and ensure the appropriate corrective actions are taken.
Assist in writing regulatory documents for FDA submission as required
Continuously monitor the manufacturing operation to look for process optimization, debottlenecking opportunities and make technical engineering recommendations and/or changes as necessary.
Prepare annual evaluation and operational assessment reports of critical systems and equipment for review and final approval.
 
Qualifications:
Bachelor’s degree in Mechanical, Biochemical, or Chemical Engineering.
Minimum 5 years of process engineering/project engineering experience in a cGMP, Pharmaceuticals, Biological manufacturing environment.
Must have the ability to apply engineering theory, practices and principles to determine root cause of equipment failures and to perform equipment performance evaluations.
 
Please apply with your updated resume.