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Biopharma Engineering Jobs (NOW HIRING)

... 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 ...

Senior MES Engineer

Fishers, IN · On-site

$94K - $129K/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 ...

Senior MES Engineer

Fishers, IN

$94K - $129K/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 ...

... 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 ...

... 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 ...

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 ...

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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:
Manufacturing Engineering Technician

Manufacturing Engineering Technician

INCOG BioPharma Services

Fishers, IN • On-site

Full-time

Posted 24 days ago


Job description

Description
The Manufacturing Engineering Technician is a key technical role within INCOG 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 candidate must have experience in pharmaceuticals and/or biologics, GMP manufacturing, and/or within highly regulated industries as well as knowledge and experience in aseptic filling, sterile manufacturing, and engineering principles.
The Manufacturing Engineering Technician will have the demonstrated ability to apply experience to process design, design thinking, data integrity, controls, instrumentation, and electro-mechanical systems.
The ideal candidate must thoroughly understand and be able to adapt to the changing needs of a manufacturing environment while providing high level support to the process engineering and operations team in troubleshooting, repair and preventative maintenance of manufacturing equipment and processes. You will be expected to work hands-on, be actively involved in continuous process improvements while taking ownership of the quality and quantity of our product. You will also be expected to demonstrate mentor and leadership skills to motivate manufacturing personnel, drive timely production activities and inspire problem solving & solution driven thinking. Additionally, this position would act as the owner of the equipment tracking process for manufacturing equipment.
Essential Job Functions:
Resolve issues that arise in day-to-day running of operations, providing timely responses and solutions.
Implement solutions in collaboration with cross-functional technical teams and site leadership team.
SME for filling equipment and supporting systems.
Evaluate and improve efficiency of manufacturing instruments, equipment, and tools.
Evaluate and implement new changes.
Participate and/or support process FMEAs to understand process and product risks as a pre-requisite for process validation.
Provide technical support to manufacturing activities.
Apply Good Engineering Practices (GEP) to drive site engineering and operational excellence.
Partner with vendors and suppliers to define requirements and understand functional specifications.
Work flexible hours to ensure production facility coverage.
Job Requirements:
Bachelor's degree in engineering field, or life sciences with 5+ years of relevant work experience.
Or 10+ years of relevant work experience.
Ability to become a SME for aseptic filling, inspection and packaging equipment.
Additional Preferences:
Lean Six Sigma Certification.
Practical expertise with cGMP manufacturing and regulatory requirements for pharmaceuticals and devices.
Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing (fill and finish), and process development.
Additional info about INCOG BioPharma Services:
At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.
If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.
INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.
By submitting your resume and details, you are declaring that the information is correct and accurate.