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Biotech Process Engineer Jobs in Columbus, OH (NOW HIRING)

Senior Mechanical Engineer

Columbus, OH ยท On-site

$150 - $160/hr

Our teams partner with leading pharmaceutical and biotechnology companies to deliver manufacturing ... Develop engineering solutions for process utilities, manufacturing support infrastructure, facility ...

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Biotech Process Engineer information

See Columbus, OH salary details

$47.8K

$88.9K

$137.6K

How much do biotech process engineer jobs pay per year?

As of Aug 24, 2026, the average yearly pay for biotech process engineer in Columbus, OH is $88,880.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $99,500.00 per year, depending on experience, location, and employer.

What does a Biotech Process Engineer do?

A Biotech Process Engineer designs, develops, and optimizes processes used in the production of biological products such as pharmaceuticals, vaccines, and biofuels. They work closely with scientists and manufacturing teams to scale up lab procedures to industrial levels while ensuring product quality and regulatory compliance. Their role often involves troubleshooting equipment, improving efficiency, and implementing new technologies within biotech manufacturing environments.

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

To thrive as a Biotech Process Engineer, you need a solid background in chemical or biochemical engineering, process design, and regulatory compliance, typically supported by a relevant bachelor's or master's degree. Familiarity with process control systems, bioprocess simulation software, and industry-standard quality systems such as cGMP is essential. Strong analytical thinking, problem-solving abilities, and effective teamwork and communication skills help you excel in cross-functional environments. These skills ensure efficient, compliant, and innovative bioprocess operations, which are critical for product quality and organizational success.

What are some common challenges faced by Biotech Process Engineers during scale-up from laboratory to production?

Biotech Process Engineers often encounter challenges when scaling up processes from laboratory or pilot scale to full production. These challenges can include maintaining product consistency, ensuring process sterility, and adapting equipment to handle larger volumes without compromising yield or quality. Engineers must also collaborate closely with cross-functional teams such as quality assurance, validation, and manufacturing to implement changes efficiently and adhere to regulatory standards. Proactive problem-solving and strong communication skills are key to overcoming these hurdles and ensuring successful technology transfer.

What is the difference between Biotech Process Engineer vs Biotech Manufacturing Technician?

AspectBiotech Process EngineerBiotech Manufacturing Technician
CredentialsBachelor's degree in biotech, chemical engineering, or related field; often requires experience in process designAssociate's or bachelor's degree; focus on operational skills and equipment handling
Work EnvironmentDesigning, optimizing, and overseeing production processes in labs or manufacturing facilitiesOperating and maintaining equipment on the manufacturing floor
Job FocusProcess development, scale-up, troubleshooting, and process improvementExecuting production tasks, quality checks, and equipment setup

Biotech Process Engineers focus on designing and improving manufacturing processes, requiring technical and analytical skills. In contrast, Biotech Manufacturing Technicians handle day-to-day production operations. Both roles are essential in biotech manufacturing but differ in responsibilities and required qualifications.

What job categories do people searching Biotech Process Engineer jobs in Columbus, OH look for?

The top searched job categories for Biotech Process Engineer jobs in Columbus, OH are:

Infographic showing various Biotech Process Engineer job openings in Columbus, OH as of August 2026, with employment types broken down into 69% Full Time, and 31% Contract. Highlights an 94% In-person, and 6% Hybrid job distribution, with an average salary of $88,880 per year, or $42.7 per hour.

Manufacturing Specialist-Process Engineer

New Albany, OH โ€ข On-site

$108 - $146/hr

Other

Medical, Dental, Vision, Life, Retirement

Posted 22 hours ago

Posted today


Job description

Career Category Manufacturing Job Description Job Description

Join Amgenโ€™s Mission of Serving Patients

At Amgen, if you feel like youโ€™re part of something bigger, itโ€™s because you are. Our shared missionโ€”to serve patients living with serious illnessesโ€”drives all that we do. Since 1980, weโ€™ve helped pioneer the world of biotech in our fight against the worldโ€™s toughest diseases. With our focus on four therapeutic areas โ€“Oncology, Inflammation, General Medicine, and Rare Diseaseโ€“ we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesityโ€‘related conditions. As a member of the Amgen team, youโ€™ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our awardโ€‘winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youโ€™ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Specialist, ManufacturingWhat you will do

Letโ€™s do this. Letโ€™s change the world. This role will support the execution of manufacturing/quality systems such as continuous improvement, technology transfer / new product introductions, process validation, manufacturing process/procedures, risk assessments, training, and nonโ€‘conformance. They will apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support operations. You may also serve as the primary production process owner for process support systems and assist with process ownership responsibilities on process systems.

Responsibilities may include, but are not limited to
  • Applied Process Expertise: As a document owner, initiate, revise, and approve manufacturing procedures to ensure all procedures reflect current operations. Assess process performance by; observation of floor operations, review of performance data and provide troubleshooting support. Evaluate, plan, and implement solutions for process improvement opportunities. Assist in generation of training materials and / or in providing training on scientific or technical aspects of the process. Complete risk evaluations for new processes or changes to existing processes and issue the summary reports of these evaluations.
  • Projects and Initiatives: Bring continuous improvement initiatives for cost reduction or cycle time reduction and participate in the assessment or implementation of such special projects or initiatives.
  • Process Monitoring: Support process monitoring parameters and control limits based off critical metrics and recommend improvements. Collect processโ€‘monitoring data and support the assessment of deviations. Provide support of timely process monitoring quarterly reports.
  • Technology Transfer / New Product Introductions & Process or Equipment Modifications: Participate in technology transfer / NPI process to assess requirements for documentation, materials, training, and equipment modifications. Assess, prioritize, justify, and provide implementation and project management support for process or equipment modification projects.
  • Nonโ€‘Conformance and CAPA: Ensure that all Nonโ€‘conformance are triage within the established goal. Assist with investigations, corrective actions and NC/CAPA closure within established goal. Monitor and communicate incidents trends. Review equipment/system Root Cause Analysis investigations and support trend evaluations.
  • Process Validation: Assist with the process validation and generation of process validation protocols and reports. Support collection and analysis of process validation data.
  • Regulatory: May participate in regulatory inspections.
  • Change Control: As manufacturing change owner, provide assessments on CCRB records impacting the process.
What we expect of you

We are all different, yet we all use our outstanding contributions to serve patients. The professional we seek will possess these qualifications.

Basic Qualifications
  • Doctorate degree
  • Or Masterโ€™s degree and 2 years in Engineering, Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.
  • Or Bachelorโ€™s degree and 4 years in Engineering, Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.
  • Or Associateโ€™s degree and 8 years in Engineering, Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.
  • Or High school diploma / GED and 10 years in Engineering, Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.
Preferred Qualifications
  • Detailed technical understanding of bioโ€‘processing and manufacturing operations
  • Develop, manage, and implement process improvements
  • Experience with Lean principals (Kaizen, Six Sigma, Operational Excellence) and knowledge of problemโ€‘solving techniques
  • Experience in participating and helping lead crossโ€‘functional teams
  • Collaborate with staff at all levels in the organization, including technical and management staff within manufacturing, process development, and quality
  • Experience with change control process and change management
  • Skilled in performance of GMP production operations
  • Regulatory knowledge and interactions
  • Project management skills
  • Excellent organizational, technical writing, presentation, and verbal skills
  • Knowledge of data analysis and control charting

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Sponsorship

Sponsorship for this role is not guaranteed. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and wellโ€‘being. From our competitive benefits to our collaborative culture, weโ€™ll support your journey every step of the way.

  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a salesโ€‘based incentive plan
  • Stockโ€‘based longโ€‘term incentives
  • Awardโ€‘winning timeโ€‘off plans
  • Flexible work models where possible.
Salary Range

107,545.40USD -145,502.60 USD

Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve peopleโ€™s lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen.

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