1

Biotech Engineering Jobs in Indiana (NOW HIRING)

Be Seen First

We are seeking a motivated Manufacturing Engineer to support manufacturing operations, process improvements, and production activities. This is an excellent opportunity for recent graduates or early ...

About Software Engineering Roles at Danaher Are you passionate about building real-world ... biotechnology. Our global teams work every day to solve the world's most complex challenges by ...

About Software Engineering Roles at Danaher Are you passionate about building real-world ... biotechnology. Our global teams work every day to solve the world's most complex challenges by ...

About Software Engineering Roles at Danaher Are you passionate about building real-world ... biotechnology. Our global teams work every day to solve the world's most complex challenges by ...

About Software Engineering Roles at Danaher Are you passionate about building real-world ... biotechnology. Our global teams work every day to solve the world's most complex challenges by ...

About Software Engineering Roles at Danaher Are you passionate about building real-world ... biotechnology. Our global teams work every day to solve the world's most complex challenges by ...

About Software Engineering Roles at Danaher Are you passionate about building real-world ... biotechnology. Our global teams work every day to solve the world's most complex challenges by ...

Project Engineer II

Munster, IN · On-site

$67K - $86K/yr

Bachelor's Degree in Construction Engineering, Management or a related field is required * Minimum ... biotechnology, and semiconductor. As one of the premier specialty construction companies in the ...

Facilities Engineer

Indianapolis, IN · On-site

$84K - $126K/yr

Bachelor's degree in engineering or related field or equivalent experience is required. * 2+ years of industrial experience is required (GMP Biotech/biopharma industry preferred) w/ Bachelor's degree ...

Bachelor's degree in Engineering, Life Sciences, or a related technical field. * Minimum 3-5 years of hands-on validation experience in the pharmaceutical, biotech, or pharmaceutical industry.

Project Engineer II

Munster, IN · On-site

$67K - $86K/yr

Bachelor's Degree in Construction Engineering, Management or a related field is required * Minimum ... biotechnology, and semiconductor. As one of the premier specialty construction companies in the ...

Project Engineer II

Munster, IN · On-site

$67K - $86K/yr

Bachelor's Degree in Construction Engineering, Management or a related field is required * Minimum ... biotechnology, and semiconductor. As one of the premier specialty construction companies in the ...

Master's degree in Science or Engineering preferred * Minimum 3years of GMP experience required * Minimum2 years of Technical Transfer experience in pharmaceutical/biotech industry * Demonstrated ...

next page

Showing results 1-20

Biotech Engineering information

See Indiana salary details

$12

$30

$54

How much do biotech engineering jobs pay per hour?

As of Jul 10, 2026, the average hourly pay for biotech engineering in Indiana is $30.02, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $36.15 per hour, depending on experience, location, and employer.

What does a typical day look like for someone working in Biotech Engineering?

A typical day in Biotech Engineering often involves a mix of hands-on laboratory experiments, data analysis, and meetings with multidisciplinary teams such as biologists, chemists, and project managers. You might spend part of your day using specialized equipment to conduct tests, followed by documenting results and discussing findings with colleagues to drive projects forward. Collaboration is key, as most projects require input from multiple areas of expertise. Additionally, you may participate in troubleshooting processes, ensuring compliance with safety protocols, and staying updated with the latest advancements in biotechnology. This dynamic environment makes every day both challenging and rewarding for professionals in the field.

What is a Biotech Engineering job?

A Biotech Engineering job involves applying principles of biology and engineering to develop technologies and products in areas like healthcare, agriculture, and pharmaceuticals. Professionals in this field work on designing medical devices, developing biopharmaceuticals, improving crop yield, and creating sustainable bio-based materials. They use techniques from genetic engineering, bioprocessing, and biomaterials science to solve complex problems. Biotech engineers often collaborate with researchers and industry experts to bring innovative solutions from the lab to real-world applications.

What are the key skills and qualifications needed to thrive in the Biotech Engineering position, and why are they important?

To thrive as a Biotech Engineer, you need a solid background in biology, chemistry, and engineering principles, often backed by a degree in biotechnology, bioengineering, or a related field. Familiarity with laboratory techniques, bioinformatics tools, and equipment such as spectrometers and PCR machines, along with relevant certifications like Six Sigma or GLP, is commonly sought after. Strong problem-solving abilities, teamwork, and clear communication distinguish top professionals in this field. These skills are essential for developing innovative solutions, ensuring regulatory compliance, and driving collaborative research in a fast-evolving industry.

What job categories do people searching Biotech Engineering jobs in Indiana look for? The top searched job categories for Biotech Engineering jobs in Indiana are:
Infographic showing various Biotech Engineering job openings in Indiana as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $62,446 per year, or $30 per hour.
6095 - CQV Engineer / Validation Engineer

6095 - CQV Engineer / Validation Engineer

Verista, Inc.

Bloomington, IN

Other

Re-posted yesterday


Job description

CQV / Validation Engineer Responsibilities:Commissioning, Qualification & Validation (CQV)
  • Execute commissioning, qualification, and validation activities for manufacturing equipment, utilities, facilities, and process systems.
  • Author, review, and execute validation lifecycle documentation including:
    • Commissioning Protocols
    • IQ (Installation Qualification)
    • OQ (Operational Qualification)
    • PQ (Performance Qualification)
    • Validation Summary Reports
    • Traceability Matrices
    • Risk Assessments
  • Support startup and operational readiness activities for new production equipment and manufacturing systems.
  • Perform field verification activities, walkdowns, and documentation reviews to ensure systems are installed and functioning according to design requirements.
  • Coordinate testing activities with Engineering, Manufacturing, Quality, and Vendor teams.
Manufacturing & Technical Support
  • Support qualification of production equipment used in pharmaceutical manufacturing operations.
  • Troubleshoot qualification and validation issues encountered during equipment startup and testing.
  • Review engineering documentation including P&IDs, equipment specifications, drawings, and vendor documentation.
  • Ensure equipment and systems meet GMP, regulatory, and internal quality requirements.
  • Assist in identifying and resolving deviations, discrepancies, and validation-related issues.
Compliance & Documentation
  • Ensure all validation activities are executed in accordance with current GMP regulations and company procedures.
  • Maintain clear, accurate, and compliant validation documentation.
  • Support change controls, deviations, CAPAs, and validation impact assessments as required.
  • Participate in audits and inspections by providing validation subject matter expertise.
Lead Validation Engineer (Additional Responsibilities)
  • Provide technical leadership and mentorship to validation team members.
  • Coordinate validation deliverables and execution schedules across multiple systems and workstreams.
  • Interface with project leadership to communicate risks, resource needs, and project status.
  • Review and approve validation documentation prepared by junior team members.
  • Drive resolution of complex qualification and startup challenges.
Requirements:
  • Bachelor's degree in Engineering, Life Sciences, or a related technical discipline.
  • 3+ years of CQV, Validation, Commissioning, or Qualification experience (Validation Engineer).
  • 7+ years of CQV, Validation, or Pharmaceutical Manufacturing experience (Lead Validation Engineer).
  • Experience supporting GMP-regulated pharmaceutical, biotech, medical device, or manufacturing environments.
  • Strong understanding of validation lifecycle principles and documentation requirements.
  • Experience authoring and executing IQ/OQ/PQ protocols.
  • Ability to work onsite in Bloomington, Indiana.
Preferred
  • Experience supporting startup of new manufacturing lines, facilities, or capital projects.
  • Experience within pharmaceutical manufacturing, sterile manufacturing, biologics, or contract manufacturing environments.
  • Familiarity with ISPE, FDA, EU GMP, and GAMP guidance.
  • Experience managing deviations, change controls, and risk assessments.
  • Strong technical writing and documentation skills.
Key Skills
  • Commissioning & Qualification (CQV)
  • Equipment Validation
  • Manufacturing Systems
  • IQ / OQ / PQ Execution
  • GMP Compliance
  • Technical Writing
  • Risk Assessments
  • Deviation Management
  • Change Control
  • Cross-Functional Collaboration
  • Startup & Operational Readiness
  • Problem Solving & Troubleshooting