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Biotech Validation Jobs in Raleigh, NC (NOW HIRING)

NCSU

Lab Manager - Biotech Teaching

Raleigh, NC

Required License or Certification N/A Valid NC Driver's License required No Commercial Driver ... Biotechnology Teaching EEO NC State University is an equal opportunity employer. All qualified ...

Cencora

Cleaning Validation Specialist

Raleigh, NC · On-site

Minimum of 5 years of professional experience in cleaning validation in the pharmaceutical and biotechnology industries. * Proficient knowledge of cleaning validation, continuous process improvement ...

Cencora

Cleaning Validation Specialist

Raleigh, NC · On-site

Minimum of 5 years of professional experience in cleaning validation in the pharmaceutical and biotechnology industries. * Proficient knowledge of cleaning validation, continuous process improvement ...

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How much do biotech validation jobs pay per hour?

As of May 29, 2026, the average hourly pay for biotech validation in Raleigh, NC is $50.54, according to ZipRecruiter salary data. Most workers in this role earn between $38.32 and $61.44 per hour, depending on experience, location, and employer.
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Biotech Validation jobs near you

Validation Engineer

Alliance Biotech Solutions LLC

Raleigh, NC • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Job Description Job Description Description: Alliance Biotech Solutions is currently hiring multiple Cleaning Validation Engineers to supports the execution and coordination of cleaning validation activities across manufacturing equipment and processes in GMP-regulated environments. This role is responsible for protocol development, execution, deviation support, and documentation while ensuring compliance with site procedures, FDA, GMP, and global regulatory standards. The Cleaning Validation Engineer will work cross-functionally with Manufacturing, Quality, Quality Control and Engineering teams to support the cleaning validation, including cycle development, hold time studies, and lifecycle management.

The role requires strong technical writing, analytical thinking, and hands-on execution. Requirements: Key Responsibilities: Execute and support cleaning validation activities, including protocol development, execution, and final report generation Support Cleaning Validation, Clean Hold Time (CHT), and Soil Hold Time (SHT) studies from planning through completion Perform on-the-floor validation execution, including sampling and coordination of cleaning activities Support cleaning validation for manufacturing equipment including process vessels, CIP systems, autoclaves, and parts washers Investigate deviations, discrepancies, and out-of-specification results; perform root cause analysis and support corrective actions Ensure timely closure of validation-related deviations and documentation Collaborate with cross-functional teams to ensure validation activities align with project timelines and operational needs Author and review validation protocols, reports, and technical documentation Support execution within electronic validation systems such as KNEAT Skills & Experience: 2+ years of experience supporting cleaning validation in GMP-regulated environments Experience with electronic validation systems such as KNEAT or similar platforms Strong understanding of GMP regulations and global compliance standards Ability to interpret technical documentation including P&IDs 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 dynamic environment Strong communication skills with the ability to collaborate cross-functionally Benefits & Compensation Industry competitive wage as a full-time employee Flexible Paid Time Off Medical, Dental and Vision Insurance with low employee cost Employer 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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