1

Biotech Engineer Jobs in Arizona (NOW HIRING)

Our client, a world leader in biotechnology and life sciences, is looking for a " Validation Engineer " based out in Tucson, AZ. Job Duration: Long Term Contract (Possibility Of Extension & FT ...

... Biotech Company is seeking a a motivated, hands-on engineer who has knowledge of/experience with ... electro-mechanical devices. Responsibilities: * Appliy intensive and diversified knowledge of ...

Senior Systems Engineer

Tucson, AZ · On-site

$100.80K - $137.90K/yr

Senior Systems Engineer A leading biotechnology company is seeking a Senior Systems Engineer to operate within the Product Development organization, specifically supporting the On Market Support (OMS ...

New

Validation Engineer

Tucson, AZ · On-site

$39 - $42/hr

We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and ... Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined ...

Software Systems Engineer Our client, a world leader in life sciences and biotechnology, is looking for a Software Systems Engineer based out of Tucson, AZ. Job Duration: Long Term Contract ...

We are seeking a proactive Validation Engineer with 1-3 years of experience in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA) to ensure compliance and ...

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 ...

next page

Showing results 1-20

Biotech Engineer information

See Arizona salary details

$34K

$100K

$128.1K

How much do biotech engineer jobs pay per year?

As of May 28, 2026, the average yearly pay for biotech engineer in Arizona is $99,974.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,500.00 and $126,700.00 per year, depending on experience, location, and employer.

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

To thrive as a Biotech Engineer, you need a solid background in biology, chemistry, and engineering principles, typically supported by a degree in biotechnology, biomedical engineering, or a related field. Familiarity with laboratory instrumentation, molecular biology techniques, and data analysis software such as MATLAB or Python is essential. Strong problem-solving skills, teamwork, and effective communication set top performers apart in this interdisciplinary role. These competencies ensure successful research, product development, and innovation in the rapidly evolving biotech sector.

What are some common challenges faced by Biotech Engineers when working on cross-disciplinary projects?

Biotech Engineers frequently collaborate with professionals from fields like biology, chemistry, and software engineering, which can present challenges in communication and aligning project goals. Understanding the specialized terminology and priorities of each discipline is essential to ensure smooth teamwork and project success. Additionally, integrating new biotechnologies with existing systems often requires adaptability and creative problem-solving. Being open to learning from colleagues and actively seeking clarification can help overcome these challenges and lead to innovative solutions.

What are Biotech Engineers?

Biotech Engineers are professionals who apply principles of biology, chemistry, and engineering to develop products and technologies that improve healthcare, agriculture, and the environment. They work on designing and optimizing processes for manufacturing pharmaceuticals, developing biofuels, engineering genetically modified organisms, and creating medical devices. Their work often involves research, laboratory experiments, and collaboration with other scientists and engineers to solve complex biological problems. Biotech Engineers play a key role in advancing innovations that benefit society and improve quality of life.

What is the difference between Biotech Engineer vs Biomedical Engineer?

AspectBiotech 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 EnvironmentBiotech companies, research labs, pharmaceutical firmsHospitals, medical device companies, research labs
Industry UsageDevelops biotech products, genetic engineering, bioprocessingDesigns medical devices, prosthetics, healthcare technology

Biotech Engineers focus on developing biotech products and processes, often working in research and manufacturing settings. Biomedical Engineers primarily design and improve medical devices and healthcare solutions. While both roles require similar educational backgrounds, their work environments and industry applications differ, catering to distinct aspects of healthcare and biotechnology.

Infographic showing various Biotech Engineer job openings in Arizona as of May 2026, with employment types broken down into 88% Full Time, and 12% Part Time. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $99,974 per year, or $48.1 per hour.
Validation Engineer

Validation Engineer

Dawar Consulting, Inc.

Tucson, AZ

$39 - $42/hr

Full-time

Medical, Dental, Vision, Retirement

Posted 5 days ago


Job description

Our client, a world leader in biotechnology and life sciences, is looking for a “Validation Engineer" based out in Tucson, AZ.

Job Duration: Long Term Contract (Possibility Of Extension & FT Conversion)

Rate: $39-$42/hr on W2

Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

Job Summary:

We are seeking a proactive Validation Engineer with 1–3 years of experience in a regulated manufacturing environment such as medical devices, pharmaceuticals, or biotechnology. This on-site role focuses on process validation activities to ensure compliance with FDA, ISO, cGMP, and internal quality standards while supporting continuous improvement and operational excellence.

Key Responsibilities:
  • Develop, write, review, and execute process validation and process verification protocols and reports
  • Conduct risk assessments and support validation strategies for new and existing manufacturing processes
  • Analyze and interpret validation data to ensure compliance with regulatory and internal quality requirements
  • Collaborate with Manufacturing, Quality, and Design Transfer teams to resolve validation issues and implement corrective actions
  • Support process optimization and continuous improvement initiatives to improve quality and efficiency
  • Ensure compliance with FDA, ISO, cGMP, and internal regulatory standards
  • Maintain validation documentation, traceability records, and audit-ready files
  • Provide training and guidance on validation processes, procedures, and compliance requirements
Required Qualifications:
  • Bachelor’s degree in Engineering, Life Sciences, or related field
  • 1–3 years of experience in validation within a regulated manufacturing environment
  • Knowledge of process validation principles, verification techniques, and industry standards
  • Familiarity with FDA regulations, ISO standards, and cGMP requirements
  • Strong technical writing, analytical, and problem-solving skills
  • Excellent communication and cross-functional collaboration abilities
Preferred Experience:
  • Medical device, biotech, or pharmaceutical industry experience
  • Experience supporting audits, CAPA activities, and process improvement initiatives
  • Familiarity with risk assessments and validation documentation practices
Key Skills:

Process Validation | Process Verification | FDA Compliance | cGMP | ISO Standards | Validation Protocols | Risk Assessments | CAPA | Technical Writing | Root Cause Analysis | Quality Systems | Continuous Improvement | Manufacturing Validation | Regulatory Compliance

If interested, please send us your updated resume at hr@dawarconsulting.com/kavitha@dawarconsulting.com .