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Biotechnology Engineer Jobs in Indiana (NOW HIRING)

Futures Consulting

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Electrical Engineer EIT

Indianapolis, IN · On-site

$85K - $115K/yr

Electrical Engineer Job Summary: The Electrical Engineer will be responsible for all aspects of ... biotech, higher education, office, and large mixed-use residential buildings and hotels. Full ...

Nooter Construction

Project Engineer

Lebanon, IN · On-site

... pharmaceutical, biotechnology, and life sciences facilities. Our success is built on safety ... The ideal Project Engineer can hit the ground running, manage multiple priorities with minimal ...

Simotechnology

Senior OSI PI Engineer

Indianapolis, IN · On-site

$90 - $120/hr

* Industry Pharma/Biotech/Clinical Research * City Indianapolis * Province Indiana * Country United ... Workcollaboratively with the System Integrator Engineers and Developers * SupportCommissioning and ...

Nooter Construction

Sr. Project Engineer

Lebanon, IN · On-site

$94K - $123K/yr

Experience supporting pharmaceutical, biotechnology, life sciences, industrial manufacturing, or ... Management, Engineering, or related field preferred. Equivalent industry experience will be ...

Stark Pharma Solutions Inc

Quality Engineer

Lafayette, IN · On-site

$69K - $89K/yr

... biotechnology, and medical device roles. I came across your profile and wanted to see if you are ... Quality Engineer Location: Lafayette, IN Duration: 6-12 Month Contract Job Summary We are seeking a ...

Danaher

Reagent Manufacturing Engineer

Indianapolis, IN · On-site

$69K - $89K/yr

... biotechnology? At Beckman Coulter Life Sciences, one of Danaher's 15+ operating companies, our work ... The Reagent Manufacturing Engineer serves as the primary engineering interface for new product ...

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All JobsBiotechnology Engineer JobsBiotechnology Engineer Jobs in Indiana

Biotechnology Engineer information

See Indiana salary details

$32.8K

$84.5K

$151.4K

How much do biotechnology engineer jobs pay per year?

As of Aug 24, 2026, the average yearly pay for biotechnology engineer in Indiana is $84,550.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,401.00 and $96,087.00 per year, depending on experience, location, and employer.

What does a biotechnology engineer do?

A Biotechnology Engineer applies principles of biology, chemistry, and engineering to develop products and technologies that improve human health, agriculture, and the environment. Their work includes designing processes for producing medicines, biofuels, and food, as well as developing equipment and systems for biotechnology applications. Biotechnology Engineers often collaborate with scientists and other engineers to innovate and solve complex biological problems, making their role crucial in advancing medical and agricultural technologies.

What are the key skills and qualifications needed to thrive as a biotechnology engineer?

To thrive as a Biotechnology Engineer, you need a strong background in biology, chemistry, and engineering principles, typically supported by a bachelor's or master's degree in biotechnology or a related field. Familiarity with laboratory equipment, bioinformatics tools, and regulatory standards such as GMP is essential. Critical thinking, problem-solving, and effective teamwork are standout soft skills in this role. These skills and qualities are crucial for developing innovative solutions and ensuring compliance in the rapidly evolving biotechnology industry.

What are some common challenges biotechnology engineers face when working on interdisciplinary teams?

Biotechnology Engineers often collaborate with professionals from biology, chemistry, computer science, and engineering backgrounds. A common challenge is bridging communication gaps due to varying technical vocabularies and priorities among disciplines. Successful engineers develop strong teamwork and communication skills to align goals, understand constraints, and integrate diverse expertise into innovative solutions. Building mutual respect and fostering open dialogue are essential for effective interdisciplinary collaboration.

What is the difference between Biotechnology Engineer vs Biomedical Engineer?

AspectBiotechnology EngineerBiomedical Engineer
Required CredentialsBachelor's or Master's in Biotechnology, Bioengineering, or related fieldsBachelor's or Master's in Biomedical Engineering, Bioengineering, or related fields
Work EnvironmentLaboratories, biotech companies, research facilitiesHospitals, medical device companies, research labs
Industry UsageBiotech firms, pharmaceutical companies, agricultural biotech
Common Search IntentComparing roles in biotech development and research

Biotechnology Engineers focus on developing and improving biotechnological products, often working in labs and biotech firms. Biomedical Engineers design medical devices and work closely with healthcare providers. While both roles require similar educational backgrounds, their work environments and industry applications differ, catering to different aspects of the life sciences sector.

Do biotechnology engineers make a lot of money?

Biotechnology engineers typically earn competitive salaries that vary based on experience, education, and location. According to industry data, the median annual wage is above the national average for engineering roles, with higher earnings possible for those with advanced skills or managerial responsibilities.

What are popular job titles related to Biotechnology Engineer jobs in Indiana?

For Biotechnology Engineer jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Biotechnology Engineer jobs in Indiana look for?

The top searched job categories for Biotechnology Engineer jobs in Indiana are:

Biotechnology Engineer jobs near you
Infographic showing various Biotechnology Engineer job openings in Indiana as of August 2026, with employment types broken down into 93% Full Time, 4% Part Time, and 3% Contract. Highlights an 84% Physical, 6% Hybrid, and 10% Remote job distribution, with an average salary of $84,550 per year, or $40.6 per hour.

Validation Engineer

Indianapolis, IN

Sterling Engineering Inc.
See more jobs at Sterling Engineering Inc.external

$75K - $120K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 17 days ago

Job description

Title: Validation Engineer - VHP / Aseptic Processing / Pharmaceutical Manufacturing
Location: Indianapolis, IN or remote in Northeast US
Hire Type: Direct Hire
Compensation: $75,000 - $120,000
Benefits: Health, Dental, Vision, 401K, PTO
Must have Skill Set:

  • Must have proven Validation Engineering experience in a pharmaceutical, biotech, life sciences, or regulated manufacturing environment.
  • Must have equipment validation experience. Cleanroom validation experience is also acceptable.
  • Must have proven experience developing and executing decontamination cycle development and validation activities.
  • Must have hands-on experience with Vaporized Hydrogen Peroxide (VHP/VPHP) systems.
  • Must have experience with Steris VHP generators or similar VHP generator systems.
  • Must have experience working in aseptic processing environments, including sterilization of equipment prior to production.
  • Must have strong pharmaceutical validation documentation experience, including validation protocols, IQ, OQ, PQ documentation, validation reports, and GMP documentation.
  • Must be willing and able to travel up to 60% to customer sites, including local day trips and overnight travel throughout the Northeastern United States.

Overview:

We are seeking an experienced Validation Engineer to support pharmaceutical, biotech, and advanced therapy manufacturing projects. This is a highly hands-on customer-facing role responsible for equipment validation, commissioning, qualification, and decontamination cycle development for aseptic manufacturing systems.

The ideal candidate will have proven experience in Validation Engineering, equipment validation, VHP (Vaporized Hydrogen Peroxide) systems, VHP cycle development, and aseptic processing environments. This individual will work closely with engineering teams and customers to execute Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities while ensuring compliance with pharmaceutical quality and regulatory requirements.

This position requires regular travel to customer sites. Candidates must be comfortable traveling up to 60%, including both local day trips and overnight travel throughout the Northeast region.

Job Duties:

  • Lead and support validation engineering activities for pharmaceutical and biotechnology manufacturing equipment.
  • Execute and support equipment validation, including FAT, SAT, IQ, OQ, and PQ activities.
  • Develop, optimize, and validate Vaporized Hydrogen Peroxide (VHP/VPHP) decontamination cycles.
  • Perform cycle development and support Performance Qualification activities related to VHP sterilization processes.
  • Work directly with customers and field service teams during equipment installation, commissioning, startup, and qualification.
  • Support validation activities within aseptic processing environments, ensuring proper sterilization of manufacturing equipment prior to production.
  • Prepare, review, and execute pharmaceutical validation documentation, including validation protocols, reports, SOPs, deviations, and change control documentation.
  • Ensure compliance with GMP, regulatory, customer, and internal quality requirements.
  • Support quality investigations, process improvements, inspections, and corrective actions.
  • Collaborate with engineering, quality, manufacturing, and customer teams throughout project execution.
  • Travel to customer facilities for validation, commissioning, startup, and qualification activities (approximately 60% travel).

Qualifications:

  • Bachelor's degree in Engineering, Life Sciences, or a related technical discipline, or equivalent industry experience.
  • Proven experience in Validation Engineering is required.
  • Proven experience with equipment validation is required.
  • Experience with cleanroom validation is acceptable in lieu of equipment validation experience.
  • Proven experience with Vaporized Hydrogen Peroxide (VHP/VPHP) systems is required.
  • Experience with Steris VHP generators is strongly preferred.
  • Proven experience developing decontamination cycles and VHP cycle development is required.
  • Experience working in aseptic processing and sterile pharmaceutical manufacturing environments is required.
  • Strong knowledge of pharmaceutical validation principles, GMP requirements, and regulated manufacturing environments.
  • Experience preparing and executing pharmaceutical documentation, including IQ/OQ/PQ protocols, validation reports, SOPs, and related quality documentation.
  • Excellent communication, problem-solving, and organizational skills.
  • Proficiency with Microsoft Office.
  • Ability and willingness to travel up to 60%, including local day travel and overnight travel throughout the Northeastern United States.


Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.