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Biotech Validation Jobs in Raleigh, NC (NOW HIRING)

Cutera

Staff Compliance Validation Engineer

Raleigh, NC · On-site

$120 - $160/hr

... biotechnology preferred). * Strong knowledge of validation principles, including IQ/OQ/PQ, with hands-on experience in software, hardware, and manufacturing environments. * Solid understanding of ...

Oxford Biomedica

Validation Engineer III

Durham, NC · On-site

We are currently recruiting for a Validation Engineer III to join our Engineering Team. In this ... OXB collaborates with some of the world's most innovative pharmaceutical and biotechnology ...

Barry Wehmiller Group

Validation Engineer

Raleigh, NC · On-site

Minimum of 1 year project experience in the pharmaceutical, life science, or biotech environments ... As a Validation Engineer, you will build a meaningful and fulfilling career with the support of ...

NCSU

Lab Manager - Biotech Teaching

Raleigh, NC · On-site

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 ...

Syner-G

Sr. Validation Engineer

Raleigh, NC

Technical Experience * 7-11 years of experience in the biotech, pharmaceutical, or medical device industry. * Strong knowledge of FDA cGMP requirements, FMEA, and riskbased validation principles.

Syner-G

Sr. Validation Engineer

Raleigh, NC · On-site

Technical Experience * 7-11 years of experience in the biotech, pharmaceutical, or medical device industry. * Strong knowledge of FDA cGMP requirements, FMEA, and risk-based validation principles.

Alliance Biotech Solutions LLC

QC Microbiologist

Raleigh, NC · On-site

$22 - $28.75/hr

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 ...

Valspec

ERP (D365) Validation Consultant

Raleigh, NC · On-site +1

We partner with a variety of sectors, including pharmaceutical, biotech, manufacturing, and other regulated industries. Position Summary: As a Microsoft D365 ERP Validation Consultant with cloud ...

Valspec

ERP (D365) Validation Consultant

Durham, NC · On-site +1

We partner with a variety of sectors, including pharmaceutical, biotech, manufacturing, and other regulated industries. Position Summary: As a Microsoft D365 ERP Validation Consultant with cloud ...

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How much do biotech validation jobs pay per hour?

As of Sep 3, 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
Infographic showing various Biotech Validation job openings in Raleigh, NC as of August 2026, with employment types broken down into 90% Full Time, 6% Part Time, and 4% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $105,133 per year, or $50.5 per hour.

Staff Compliance Validation Engineer

Cutera

Raleigh, NC • On-site

$120 - $160/hr

Other

Posted 8 days ago

Job description

Job DetailsJob Location: RALEIGH - RALEIGH, NC 27615


Position Type: Full Time


Position Summary:

We are seeking an experienced Compliance and Validation Engineer to lead validation strategy and execution across products, embedded software, hardware, and manufacturing processes. This role is critical to ensure that our technologies meet global regulatory requirements while maintaining the high standards of performance, scalability, and reliability.


As a key partner to R&D and Manufacturing, you will drive a proactive, engineering-focused approach to validation supporting new product introductions (NPI), design transfers, and sustaining operations. This role focuses on executing effective validation activities and supporting the development of efficient, scalable, and audit-ready processes.


Duties & Responsibilities:

  • Lead the development and execution of validation strategies, protocols, and reports for equipment, systems, software, and manufacturing processes.

  • Own and drive qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), with a focus on production readiness.

  • Ensure compliance with applicable regulatory and quality standards (e.g., FDA, ISO 13485) through practical, engineering-driven validation approaches.

  • Partner cross-functionally with R&D and Manufacturing teams to support new product introduction (NPI), design verification/validation, and design transfer to production.

  • Support integration and validation of hardware/software systems, including test method development and execution.

  • Drive validation activities for manufacturing equipment, fixtures, and process development to ensure robust and repeatable production.

  • Author, review, and maintain validation documentation, ensuring accuracy, completeness, and audit readiness.

  • Support internal and external audits and regulatory inspections, serving as a subject matter expert for validation and compliance activities.

  • Develop and maintain SOPs and related documentation and deliver training to ensure consistent understanding and application of validation and compliance requirements.

  • Drive continuous improvement in validation and manufacturing processes, leveraging data-driven and engineering best practices.

  • Monitor evolving regulatory requirements and industry best practices, recommending and implementing improvements as needed.

  • Other duties as needed or required.


QualificationsMinimum Requirements & Qualifications:

  • Bachelor’s degree in Engineering, Quality, or a related field; advanced degree preferred

  • 8+ years of experience in validation engineering, quality, or compliance within a regulated industry (medical device, pharmaceutical, or biotechnology preferred).

  • Strong knowledge of validation principles, including IQ/OQ/PQ, with hands-on experience in software, hardware, and manufacturing environments.

  • Solid understanding of regulatory requirements and quality standards, including FDA regulations and ISO 13485.

  • Experience with embedded systems, hardware/software integration, and production test methodologies.

  • Familiarity with supporting NPI, design transfer, and manufacturing process validation.

  • Proficiency with quality management systems (QMS) and validation documentation practices.

  • Strong analytical, problem-solving, and organizational skills with high attention to detail.

  • Excellent communication and collaboration skills, with the ability to work effectively across engineering and manufacturing teams.


Preferred Qualifications:

  • Enterprise Architect

  • Markdown

  • Quarto

  • PowerShell, JavaScript, Typst (and other tools) for automating document generation.

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