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Pharmaceutical Process Engineer Jobs (NOW HIRING)

Jubilant HollisterStier

Process Engineer, Sr.

Washington, CA · On-site

$113K - $146K/yr

Join a Leader in Pharmaceutical Manufacturing - And Build What's Next As Spokane's Largest ... The process engineer will also provide technical direction for complex projects and exhibit ...

New

Jubilant HollisterStier

Process Engineer, Sr.

Spokane, WA · On-site

$105K - $136K/yr

Join a Leader in Pharmaceutical Manufacturing - And Build What's Next As Spokane's Largest ... The process engineer will also provide technical direction for complex projects and exhibit ...

New

Actalent

Process Engineer

Elwood, KS

Process Engineer This Process Engineer role provides hands-on technical support for manufacturing ... This position offers exposure to pharmaceutical and animal health manufacturing processes ...

Actalent

Process Engineer

Clinton, TN

$48.08 - $57.69/hr

Process Engineer This Process Engineer role focuses on improving manufacturing efficiency ... Minimum 1 year of experience working in a pharmaceutical cGMP manufacturing environment. * Strong ...

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 ...

Actalent

Process Engineer

Clinton, TN

$48.08 - $57.69/hr

Process Engineer This Process Engineer role focuses on improving manufacturing efficiency ... Strong understanding of FDA-regulated manufacturing practices and pharmaceutical quality ...

Tranzeal, Inc.

Process Engineer

Paris, KY · On-site

$50 - $58/hr

... a pharmaceutical, chemical, or highly regulated cGMP manufacturing environment. Key Requirements: Bachelor's Degree in Chemical Engineering or related Engineering field 5-8 years of Process ...

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Pharmaceutical Process Engineer information

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How much do pharmaceutical process engineer jobs pay per hour?

As of Aug 17, 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 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $73,310 per year, or $35.2 per hour.

Process Engineer III, Manufacturing Sciences

Thermo Fisher Scientific

Saint Louis, MO • On-site

Other

Posted 9 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 427 frontline employees who took The Breakroom Quiz

199th of 540 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
How will you make an impact?
We are searching for a Process Engineer 3 with education and experience in biopharmaceutical processing or a related field. This member of our team provides technological input in the development, validation, and transfer of manufacturing processes. A Process Engineer 3 routinely supports the Process Engineering team as technical owners of customer programs in a manufacturing environment and will be highly involved and act as a subject matter expert in defining and shaping Thermo Fisher Scientific's own technology programs. This role will collaborate internally with supervisors and technicians in the Operations department, Quality Assurance, fellow Engineers, and scientists in Process Development and with the client as a Process Engineer program lead. These activities are conducted in projects and involve teamwork with experts across functional groups to ensure project success.
What will you do?
  • Draft, review and approve Standard Operation Procedures, and Job Aids and consult internally to ensure scientifically sound and robust procedures.
  • Collaborate with the process development to develop standardized methodologies and learn/explore new methodologies for conducting unit operations at the manufacturing scale including cell culture, harvest, and purification.
  • Contribute to Internal and Customer meetings based upon sound evidence guided by minimal supervision.
  • Manages internal projects and tasks and lead client projects and manage timelines with minimal support from supervision.
  • Actively identify error proofing opportunities and initiate and drive engineering initiatives to improve practices and procedures with minimal supervision.
  • Provide scientific expertise for GMP deviations by assessing, reviewing and approving the impact of major deviations on both the product quality and the validation of the process.
  • Lead changes to equipment and process design, proactively and with minimal supervision.
  • Draft, review and approve Manufacturing Batch Records, Performance Qualifications, Process Validation protocols, process flow diagrams, automation methods, and Bill of Materials, ensuring the process is technically accurate and designed for Manufacturing.
  • Draft, review, and approve Process control documents, campaign summary report and process validation reports
  • Reviews, analyzes and trends process data without supervision
  • Provide technical feedback on documents created by other departments, such as Tech Transfer Protocols and SOPs.
  • Troubleshoot technical challenges on the manufacturing floor as needed for a 24/7 manufacturing facility.
  • Support our MSAT team with additional tasks to improve the site, ensure patient safety, and deliver for our customers.
  • Provides development and training for Process Engineers/Scientists.

How will you get here?
Education
  • Bachelor's degree required in a scientific field, preferably an engineering field.
  • 5+ years of experience in GMP regulated Biologics / Pharma Industry, or equivalent experience (or master's degree in a scientific field + 3 years' experience or Ph.D.).

Experience
  • 5+ years of experience in GMP regulated Biologics / Pharma Industry, or equivalent experience (or master's degree in a scientific field + 3 years' experience or Ph.D.).
  • Follow Environmental, Health and Safety policies and procedures and ensure a safe and healthy workplace environment.
  • Ability to self-motivate, prioritize work and time.
  • Demonstrates a foundation in general scientific practices, principles, and concepts.
  • Writes and communicates effectively.
  • Ability to work both independently and as part of a team.
  • Knowledge of current Good Manufacturing Practices and EU regulations.
  • Intermediate knowledge of statistical methods used for Pharmaceutical Process Analysis is a plus.
  • Proficient in Microsoft Word and Excel.
  • Ability to stand for prolonged periods of time and gown into manufacturing areas.

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