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Pharmaceutical Engineer Jobs (NOW HIRING)

The International Society for Pharmaceutical Engineering, Inc.

$140 - $190/hr

Lead CQV Engineer - Pharmaceutical Manufacturing - Major CAPEX Projects A global pharmaceutical manufacturer is looking for an experienced Lead CQV Engineer to play a key role in the delivery of ...

Jubilant Pharma, LLC

$84 - $135/hr

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

Jubilant Pharma, LLC

Engineer I, Project

Spokane, WA · On-site

$84 - $135/hr

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

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Pharmaceutical Engineer information

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How much do pharmaceutical engineer jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for pharmaceutical engineer in the United States is $38.46, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $40.38 per hour, depending on experience, location, and employer.

What does a pharmaceutical engineer do?

Pharmaceutical engineers design and manufacture pharmaceutical products. As a pharmaceutical engineer, the focus of your work may be on chemical research, manufacturing design, field testing, quality assurance, packaging and labeling, product delivery, or regulations compliance. Your job duties include collaborating with other engineers and manufacturing personnel, and ensuring all procedures follow Good Manufacturing Practice Regulations established by the Food and Drug Administration (FDA). You need extensive science experience, strong analytical and problem-solving skills, and the ability to work well with a team.

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

To thrive as a Pharmaceutical Engineer, you need a strong background in chemical or biomedical engineering, pharmaceutical sciences, and process development, typically supported by a relevant bachelor's or master's degree. Familiarity with Good Manufacturing Practice (GMP) regulations, process simulation software, and quality assurance systems is essential. Exceptional problem-solving, attention to detail, and teamwork skills help you excel in cross-functional environments. These skills ensure safe, efficient drug production and regulatory compliance, which are vital for patient safety and business success.

How do pharmaceutical engineers typically collaborate with cross-functional teams during drug development projects?

Pharmaceutical engineers work closely with scientists, quality assurance specialists, regulatory teams, and manufacturing staff throughout the drug development process. They play a key role in translating laboratory-scale processes into safe, efficient, and scalable manufacturing solutions. Effective communication and teamwork are crucial, as engineers must ensure that all technical, safety, and compliance requirements are met while balancing project timelines and budgets. This collaborative environment offers valuable opportunities to broaden your expertise and develop leadership skills, especially as you take on more responsibility in project management or process optimization roles.

What is the difference between Pharmaceutical Engineer vs Chemical Engineer?

AspectPharmaceutical EngineerChemical Engineer
CredentialsBachelor's in Pharmaceutical Engineering, Chemical Engineering, or related field; often requires industry-specific certificationsBachelor's in Chemical Engineering; professional engineer (PE) license optional
Work EnvironmentPharmaceutical manufacturing facilities, labs, quality controlChemical plants, refineries, research labs
Industry UsagePrimarily in pharmaceutical and biotech industriesBroader industries including chemicals, energy, and materials
Job FocusDesigning and optimizing drug manufacturing processes, ensuring compliance with regulationsDesigning chemical processes, scaling up production, safety analysis

While both roles require a background in chemical processes, Pharmaceutical Engineers focus specifically on drug manufacturing and regulatory compliance within the pharmaceutical industry. Chemical Engineers have a broader scope, working across various chemical production sectors. The choice depends on your industry interest and specialization goals.

More about Pharmaceutical Engineer jobs

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Pharmaceutical Engineer jobs near you
Infographic showing various Pharmaceutical Engineer job openings in the United States as of August 2026, with employment types broken down into 93% Full Time, 3% Part Time, and 4% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $79,999 per year, or $38.5 per hour.

Process Engineer II (Pharmaceutical Manufacturing)

Astrix Inc

Wilmington, OH • On-site

Full-time

Re-posted 10 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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