Bausch Health
Bausch Health

62 Bausch Health Validation Engineer Jobs Hiring Near You

... of healthcare and technology alongside a purpose-driven, supportive team. Excited to build ... Validation & Engineering Group is an equal opportunity employer. All applicants will be considered ...

... of healthcare and technology alongside a purpose-driven, supportive team. Excited to build ... Validation & Engineering Group is an equal opportunity employer. All applicants will be considered ...

... of healthcare and technology alongside a purpose-driven, supportive team. Excited to build ... Validation & Engineering Group is an equal opportunity employer. All applicants will be considered ...

... of healthcare and technology alongside a purpose-driven, supportive team. Excited to build ... Validation & Engineering Group is an equal opportunity employer. All applicants will be considered ...

Validation Engineer

Wilson, NC · On-site

$85 - $120/hr

... of healthcare and technology alongside a purpose-driven, supportive team. Excited to build ... Validation & Engineering Group is an equal opportunity employer. All applicants will be considered ...

$85 - $130/hr

... of healthcare and technology alongside a purpose-driven, supportive team. Excited to build ... Validation & Engineering Group is an equal opportunity employer. All applicants will be considered ...

... of healthcare and technology alongside a purpose-driven, supportive team. Excited to build ... Validation & Engineering Group is an equal opportunity employer. All applicants will be considered ...

... of healthcare and technology alongside a purpose-driven, supportive team. Excited to build ... Validation & Engineering Group is an equal opportunity employer. All applicants will be considered ...

Validation Engineer Location: Framingham, MA What's the Job? * Lead and execute equipment ... Health Savings Account * Health Flexible Spending Account * Dependent Care Flexible Spending ...

The Validation Engineer will work under limited supervision to support product validation and ... Ensure compliance with Health, Safety, Environmental, and regulatory requirements. * Maintain ...

As a Validation Engineer 3, you will be part of a highly technical team supporting processor ... Health Savings Account * Health Flexible Spending Account * Dependent Care Flexible Spending ...

As a Validation Engineer, you will be part of the Systems Engineering department supporting ... Health Savings Account * Health Flexible Spending Account * Dependent Care Flexible Spending ...

... of healthcare and technology alongside a purpose-driven, supportive team. Excited to build ... Validation & Engineering Group is an equal opportunity employer. All applicants will be considered ...

Validation Engineer Job Location: Raleigh - North Carolina Job Type: Contract * Manage lab servers ... Monitor lab health and resolve system or network issues promptly * Maintain lab inventory and ...

Validation Engineer As a Validation Engineer, you will deeply review and understand customer ... Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off ...

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Bausch Health Jobs Information

What is it like to work at Bausch Health?

Bausch Health is a global company that values innovation, collaboration, and patient-centricity, fostering a culture that prioritizes teamwork and open communication.

The company's structure is organized into various business units, each focused on a specific therapeutic area, allowing employees to work closely with cross-functional teams and contribute to the development of new treatments and products. Bausch Health's global headquarters is located in Burlington, Ontario, Canada, and the company operates in a fast-paced environment that encourages adaptability and continuous learning.

Working at Bausch Health may appeal to candidates who are passionate about making a difference in people's lives through innovative healthcare solutions, as the company offers opportunities for professional growth, development, and contributions to the advancement of medical science and patient care.

What makes Bausch Health an attractive place to work?

Bausch Health is a leading global company in the pharmaceutical and healthcare industry, with a diverse portfolio of brands and a commitment to improving the lives of patients worldwide. The company offers a dynamic work environment that fosters innovation, collaboration, and professional growth, with opportunities to work on cutting-edge projects and develop new skills. By joining Bausch Health, individuals can contribute to the company's mission of delivering innovative solutions and making a meaningful impact in the healthcare industry, while also advancing their careers and achieving their personal and professional goals.

What other companies are hiring for Validation Engineer jobs?

What are the most popular categories at Bausch Health?

Infographic showing various Validation Engineer job openings at Bausch Health in the United States as of August 2026, with employment types broken down into 98% Full Time, and 2% Part Time. Highlights an 100% Physical job distribution.

Validation Engineer

Pinnaql

Wilson, NC • On-site

Full-time

Posted 13 days ago


Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
  • Validation Engineer

Position Overview
We are seeking an experienced Validation Engineer with Commissioning, Qualification & Validation (CQV) experience to support projects within the life sciences industry. The successful candidate will be responsible for executing and documenting commissioning, qualification, and validation activities for facilities, utilities, equipment, systems, and manufacturing processes in accordance with applicable regulatory requirements and Good Manufacturing Practices (GMP).
This role requires strong technical documentation skills, attention to detail, and the ability to work collaboratively with Engineering, Quality, Manufacturing, Automation, and Project Management teams.
Key Responsibilities
  • Execute and support Commissioning, Qualification & Validation (CQV) activities for pharmaceutical, biotechnology, medical device, or other regulated life sciences facilities.
  • Develop, review, and execute validation documentation, including:
    • Validation Plans
    • User Requirements Specifications (URS)
    • Risk Assessments
    • Design/Functional Specifications
    • Commissioning documentation
    • IQ/OQ/PQ protocols and reports
    • Traceability Matrices
    • Summary Reports
  • Support qualification of equipment, facilities, utilities, and manufacturing systems.
  • Perform protocol execution, field verification, data collection, and review of qualification results.
  • Ensure validation activities are performed in compliance with GMP, FDA, EU GMP, and applicable industry standards.
  • Participate in FMEA/risk assessments and apply a risk-based approach to validation activities.
  • Support deviations, investigations, CAPA, and change control activities associated with validation projects.
  • Review engineering and technical documentation to ensure validation requirements are adequately addressed.
  • Collaborate with Engineering, Quality Assurance, Manufacturing, Automation, Facilities, and other project stakeholders.
  • Track validation deliverables, schedules, open items, and project milestones.
  • Support commissioning activities and transition from commissioning into formal qualification.
  • Ensure validation documentation is complete, accurate, and audit-ready.
  • Participate in client meetings, project status meetings, and technical reviews.
  • Provide technical support during regulatory or client inspections, as required.

CQV Experience
Candidates should have hands-on experience with some combination of:
  • Commissioning and qualification of process equipment
  • Facility and utility qualification
  • Cleanrooms and controlled environments
  • HVAC systems
  • Purified Water / WFI systems
  • Compressed gases and process gases
  • Autoclaves, sterilizers, and/or depyrogenation equipment
  • Manufacturing and laboratory equipment
  • Temperature-controlled systems
  • Process systems and supporting utilities
  • Equipment and system turnover documentation
  • IQ/OQ/PQ execution

Required Qualifications
  • Bachelor's degree in Engineering, Science, or a related technical discipline.
  • 3+ years of validation, qualification, commissioning, or CQV experience within a regulated life sciences environment.
  • Experience working in pharmaceutical, biotechnology, medical device, or other GMP-regulated industries.
  • Strong understanding of GMP and validation principles.
  • Experience developing and/or executing validation and qualification protocols.
  • Experience with risk-based validation methodologies.
  • Strong technical writing and documentation skills.
  • Ability to interpret engineering drawings, specifications, procedures, and technical documentation.
  • Strong organizational and project management skills.
  • Ability to work independently and collaboratively in a project environment.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.