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How much do biotech engineering jobs pay per hour?

As of May 28, 2026, the average hourly pay for biotech engineering in Raleigh, NC is $28.12, according to ZipRecruiter salary data. Most workers in this role earn between $17.98 and $33.85 per hour, depending on experience, location, and employer.

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 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.
More about Biotech Engineering jobs
What are popular job titles related to Biotech Engineering jobs in Raleigh, NC? For Biotech Engineering jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Biotech Engineering jobs in Raleigh, NC look for? The top searched job categories for Biotech Engineering jobs in Raleigh, NC are:
Biotech Engineering jobs near you

Equipment Validation Engineer

Alliance Biotech Solutions LLC

Raleigh, NC • On-site

Full-time

Dental, Vision, Retirement, PTO

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Alliance Biotech Solutions has multiple openings for Validation Engineers to support the execution and coordination of commissioning, qualification, and validation (CQV) activities for new and existing equipment within a GMP-regulated CDMO environment. These roles will focus on the introduction of new process equipment and updates to existing systems, ensuring all validation activities are executed in compliance with FDA, GMP, and global regulatory standards.
This Validation Engineer will work cross-functionally with Manufacturing, Quality, Engineering, and Automation teams to support equipment qualification, system integration, and potential CSV activities. The role requires strong technical writing, analytical thinking, and hands-on execution to ensure compliant, efficient project delivery within aggressive timelines.
Requirements
• Execute and support equipment qualification activities including IQ/OQ/PQ protocol development, execution, and report generation
• Support validation efforts for single-use systems including single-use mixers (SUMs), process pumps, and filtration systems (SUTFF)
• Participate in the qualification of lab instruments such as cell viability analyzers (e.g., Vi-Cell BLU) including potential CSV/data integrity support
• Perform on-the-floor validation execution including system walkdowns, functional testing, and coordination with operations
• Support system integration activities, ensuring equipment and instrumentation operate within defined parameters
• Assist with updates and modifications to existing systems, including parameter and instrumentation changes
• Investigate deviations, discrepancies, and non-conformances; perform root cause analysis and support corrective actions
• Ensure timely closure of validation deliverables and associated documentation
• Collaborate with cross-functional teams to align validation activities with project timelines and operational priorities
• Author and review validation protocols, reports, and technical documentation
• Support execution within electronic validation and quality systems (e.g., KNEAT, TrackWise, Veeva or similar)
Experience/Skills
• 2+ years (mid-level) or 5+ years (senior) of experience supporting CQV/validation activities in GMP-regulated environments
• Experience with equipment qualification (IQ/OQ/PQ) for manufacturing and/or lab systems
• Exposure to single-use technologies and/or biopharmaceutical manufacturing environments preferred
• Experience with CSV and data integrity concepts is a plus
• Strong understanding of GMP regulations and global compliance standards
• Ability to interpret technical documentation including P&IDs, URS, and process flow diagrams
• Strong technical writing and documentation skills
• Demonstrated analytical and problem-solving capabilities
• Ability to work independently and manage multiple priorities in a fast-paced project environment
• Strong communication skills with the ability to collaborate cross-functionally
Benefits & Compensation
• Competitive wage as a full-time employee
• Paid Time Off
• Dental and Vision Insurance with low employee cost
• 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.

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