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Biopharma Engineering Jobs (NOW HIRING)

INCOG

Senior MES Engineer

Fishers, IN · On-site

$97K - $134K/yr

... BioPharma Engineering and Technical Operations to ensure data integrity, implement state-of-the-art digital technologies, process control strategies, and support the technology road map. The ideal ...

Twist BioScience

Project Manager, Biopharma

Communication with customers, the Antibody Engineering and Protein Production teams, the Business ... the Biopharma Project Team in response to all customer and internal inquiries; maintain ...

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Biopharma Engineering information

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$46.5K

$146.9K

$174K

How much do biopharma engineering jobs pay per year?

As of Jun 8, 2026, the average yearly pay for biopharma engineering in the United States is $146,868.00, according to ZipRecruiter salary data. Most workers in this role earn between $116,500.00 and $173,000.00 per year, depending on experience, location, and employer.

What are common challenges faced by biopharma engineers when scaling up processes from lab to production?

One of the main challenges biopharma engineers encounter is ensuring that processes developed at the laboratory scale can be successfully and safely transferred to large-scale manufacturing. This often involves addressing differences in equipment, maintaining product quality, and ensuring regulatory compliance. Collaborative troubleshooting with cross-functional teams—such as quality assurance, process development, and manufacturing operations—is essential. Additionally, engineers must adapt to evolving technologies while meeting strict timelines, making adaptability and strong communication skills key to success.

What is biopharma engineering?

Biopharma engineering is a specialized field that combines principles of biology, chemistry, and engineering to design, develop, and optimize processes for producing biopharmaceutical products, such as vaccines, therapeutic proteins, and gene therapies. Professionals in this field work on scaling up laboratory processes to industrial production, ensuring product quality, safety, and regulatory compliance. Biopharma engineers play a critical role in bringing new medical treatments to market by improving manufacturing efficiency and innovation.

What is the difference between Biopharma Engineering vs Bioprocess Technician?

AspectBiopharma EngineeringBioprocess Technician
Required CredentialsBachelor's degree in bioengineering, chemical engineering, or related fieldAssociate's or bachelor's degree in biotechnology, biology, or related field
Work EnvironmentDesign, develop, and optimize biopharmaceutical manufacturing processesOperate and monitor bioprocess equipment on production lines
Employer & Industry UsagePharmaceutical companies, biotech firms, research institutionsManufacturing plants, biotech companies, contract manufacturing organizations

Biopharma Engineering focuses on designing and improving biopharmaceutical processes, requiring engineering expertise. In contrast, Bioprocess Technicians handle daily operations and equipment in production settings. Both roles are essential in the biopharma industry but differ in responsibilities and qualifications.

What does a biopharmaceutical engineer do?

A biopharmaceutical engineer designs and develops processes for producing biological drugs, such as vaccines and therapies, often working in laboratory and manufacturing environments. They utilize skills in biotechnology, chemical engineering, and quality control to ensure safe and efficient production, frequently working with equipment like bioreactors and adhering to regulatory standards.

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

To thrive as a Biopharma Engineer, you need a solid background in biochemical engineering, process development, and regulatory compliance, typically supported by a degree in chemical, biomedical, or bioprocess engineering. Familiarity with GMP standards, bioreactor operations, and software like MATLAB or process simulation tools is essential. Strong problem-solving abilities, teamwork, and effective communication help you excel in cross-functional environments. These skills ensure the efficient and compliant production of biopharmaceutical products, which is vital for patient safety and company success.
More about Biopharma Engineering jobs
What states have the most Biopharma Engineering jobs? States with the most job openings for Biopharma Engineering jobs include:
What job categories do people searching Biopharma Engineering jobs look for? The top searched job categories for Biopharma Engineering jobs are:
Biopharma Engineering jobs near you

Automation Engineer

PharmEng Technology Americas

Durham, NC • On-site

Contractor

Posted 25 days ago

Job description

PharmEng Technology is a global ISO certified Pharmaceutical Compliance Consulting Firm with projects around the world providing quality services to the manufacturers of pharmaceutical and health care products for over 25 years.


Our 300+ global consultants have expertise in Commissioning & Qualification, Validation, Quality Systems, Engineering, Medical Devices, Modular Cleanrooms, Thermal Mapping, Training, Toxicology and Regulatory Affairs.


PharmEng Technology is a cGMP compliant leader with international offices in Canada, Spain, France, Germany, Austria, Switzerland, Italy, Belgium, Singapore, Malaysia, Indonesia, Taiwan, Ireland, Denmark, Brazil and USA and maintains strategic partnerships for extended capabilities internationally.


PharmEng Technologies is seeking a full-time experienced Automation Engineer in Durham, NC


The Automation Hardware Engineer will oversee the system integrator design, construction, and configuration of the DeltaV platform. This includes but is not limited to:


  • DeltaV Server infrastructure, host servers, thin clients, controllers
  • DeltaV Firewalls, switches
  • DeltaV Virtual Machines
  • DeltaV physical integration with external systems (BMS, PLC)


The specifications and testing are being executed by a System Integrator (SI), and this role is to provide technical oversight of the SI, review and approve documents the SI produces, and in general represent the client’s interests.


The platform engineer is also responsible for establishing standard work practices with the SI, such as configuration management practices, and testing practices, and will have responsibility for reviewing, evaluating, and impact assessments of changes.


Responsibilities


  • Possess a deep understanding of the DeltaV platform
  • Possess a deep understanding of DeltaV control system design in the pharmaceutical industry.
  • Technically Lead and oversee the work and work products that the System Integrator produces. Including (but not limited to): technical standards, work processes.
  • Work collaboratively with the System Integrator Engineers and Developers


Qualifications


  • BS Engineering (or equivalent experience)
  • Preferable, 7 years working experience in Biopharma engineering, operations, or manufacturing.
  • Preferable, 5 years’ experience in DeltaV control system design.
  • Preferable, Instrumentation knowledge.
  • Demonstrated technical leadership and teamwork abilities.
  • Knowledge of GMP’S, regulatory requirements, computer system validation.
  • Interface regularly and provide formal and informal project status updates to Project Management.
  • Good written and verbal communication skills for both technical and non-technical audiences.