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Biopharmaceutical Engineering Jobs (NOW HIRING)

INCOG BioPharma Services

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 ...

INCOG BioPharma Services

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 ...

INCOG BioPharma Services

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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Biopharmaceutical Engineering information

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How much do biopharmaceutical engineering jobs pay per year?

As of Jun 23, 2026, the average yearly pay for biopharmaceutical engineering in the United States is $92,956.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,500.00 and $114,000.00 per year, depending on experience, location, and employer.

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

To thrive as a Biopharmaceutical Engineer, you need a solid background in chemical or biomedical engineering, biological sciences, and regulatory knowledge, often supported by a relevant degree. Familiarity with bioprocessing equipment, Good Manufacturing Practices (GMP), and software such as process simulation tools is typically required. Strong problem-solving, teamwork, and communication skills set top professionals apart in this field. These competencies are crucial for ensuring safe, efficient, and compliant development and production of biopharmaceutical products.

What does a biopharmaceutical engineer do?

A biopharmaceutical engineer designs and develops processes for producing biological drugs and therapies, ensuring they are safe, effective, and scalable. They work with bioreactors, purification systems, and quality control methods, often using tools like chromatography and fermentation technology, and typically require knowledge of regulatory standards such as GMP.

What are some common challenges faced by biopharmaceutical engineers when working on new drug development projects?

Biopharmaceutical engineers often encounter challenges related to balancing innovation with regulatory compliance during new drug development. They must ensure that all processes meet strict quality and safety standards while also optimizing production efficiency. Additionally, they frequently collaborate with cross-functional teams, including scientists, quality assurance, and manufacturing, to address issues such as scalability and process validation. Staying current with evolving technologies and adapting to changes in project requirements are also common aspects of the role.

What is biopharmaceutical engineering?

Biopharmaceutical engineering is a multidisciplinary field that combines principles of biology, chemistry, and engineering to design, develop, and manufacture biopharmaceutical products such as vaccines, therapeutic proteins, and monoclonal antibodies. Professionals in this field work on optimizing the processes for producing biologically-derived drugs, ensuring they are safe, effective, and meet regulatory standards. Biopharmaceutical engineers play a critical role in translating scientific discoveries into scalable, market-ready medicines that can improve patient health worldwide.

What engineers make $500,000?

In biopharmaceutical engineering, senior-level engineers with extensive experience, advanced degrees, and specialized skills in areas like process development or regulatory compliance can reach or exceed $500,000 annually, especially in leadership roles or with bonuses and stock options. Such compensation typically requires years of expertise, a strong track record, and often working in high-cost regions or large companies.

What is the difference between Biopharmaceutical Engineering vs Bioprocess Technician?

AspectBiopharmaceutical EngineeringBioprocess Technician
Required CredentialsBachelor's or higher in bioengineering, chemical engineering, or related fieldsAssociate's or bachelor's degree in biotechnology, biology, or related fields
Work EnvironmentDesign, develop, and optimize biopharmaceutical processes in labs and manufacturing facilitiesOperate and monitor bioprocess equipment on production lines
Industry UsageResearch, development, and process design in pharmaceutical companiesManufacturing and quality control in biopharma production plants

Biopharmaceutical Engineering focuses on designing and improving bioprocesses, requiring advanced degrees and a broader scope. In contrast, Bioprocess Technicians primarily operate and monitor manufacturing equipment, often with technical diplomas. Both roles are essential in the biopharmaceutical industry but differ in responsibilities and qualifications.

What engineers make $300,000 a year?

In biopharmaceutical engineering, senior-level professionals such as lead process engineers, R&D directors, or engineering managers can earn $300,000 or more annually, especially with extensive experience, advanced degrees, and specialized skills in areas like bioprocessing, regulatory compliance, or automation. High compensation often reflects leadership roles, complex project management, and industry demand for expertise in developing and manufacturing biopharmaceutical products.

What jobs can a bio engineer get?

A bioengineer can pursue roles such as biomedical engineer, bioprocess engineer, research scientist, quality assurance specialist, or regulatory affairs associate. These positions often require knowledge of biology, engineering principles, and laboratory or manufacturing environments, with certifications like PE or advanced degrees enhancing job prospects.
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Biopharmaceutical Engineering jobs near you

QC Microbiology Consultant

ALLIANCE BIOTECH SOLUTIONS LLC

Wilson, NC

$22.25 - $29.25/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago

Job description

Description

Alliance Biotech Solutions is seeking an experienced QC Microbiology Consultant to support a large-scale method transfer remediation and validation program at a pharmaceutical manufacturing facility. This role will focus on the assessment, remediation, transfer, and validation of legacy microbiological methods to ensure compliance with current GMP requirements and regulatory expectations.

Requirements

Responsibilities

Evaluate and remediate legacy microbiological methods.
Support method transfer and validation activities.
Author protocols, risk assessments, and reports.
Review historical data and identify compliance gaps.
Troubleshoot microbiological methods and support investigations.
Train analysts and support knowledge transfer activities.
Generate GMP documentation and final reports.
Partner with QC and QA teams to ensure regulatory compliance.


Experience/Skills

Bachelor's degree in Microbiology, Biology, Biochemistry, or a related life sciences discipline.
5+ years of experience in Quality Control Microbiology within a pharmaceutical, biotechnology, or regulated GMP environment.
Demonstrated experience supporting microbiological method transfers, method validation, method verification, or remediation activities.
Strong experience authoring protocols, risk assessments, investigations, technical reports, and GMP documentation.
Proven ability to troubleshoot microbiological methods and investigate atypical results.


Benefits & Compensation

Industry competitive wage as a full-time employee

Flexible Paid Time Off

Medical, Dental and Vision Insurance with low employee cost

Employer paid long term and short-term disability

401k plan with employer contributions


About Alliance Biotech Solutions

Alliance Biotech Solutions (ABS) is a premier consulting firm specializing in biopharmaceutical engineering and validation services. As industry leaders in Commissioning, Qualification, and Validation (CQV), we provide crucial services to the biotech and pharmaceutical sectors while maintaining our philosophy that employees are our #1 priority. Our success is built on the foundation of empowering our team members' growth and development, recognizing that our employees are the cornerstone of our clients' success.

Alliance Biotech Solutions is an Equal Employment Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, ancestry, citizenship status, military status, protected veteran status, religion, creed, physical or mental disability, medical condition, marital status, sex, sexual orientation, gender, gender identity or expression, age, genetic information, or any other basis protected by law, ordinance, or regulation.

Alliance Biotech Solutions does not accept unsolicited resumes through or from search firms or staffing agencies. All unsolicited resumes will be considered the property of Alliance Biotech Solutions, and Alliance Biotech Solutions will not be obligated to pay a placement fee.

All persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.

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