Bausch Health
Bausch Health

62 Bausch Health Validation Engineer Jobs Hiring Near You

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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

Validation & Engineering Group, Inc

Holly Springs, NC • On-site

Full-time

Re-posted 14 days ago


Job description

Validation & Engineering Group, Inc. (V&EG) 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

Description:

The role demands deep technical expertise across the full validation lifecycle — including URS development, FAT/SAT execution, and Computer System Validation (CSV) — as well as hands-on experience with systems and controls integration. The candidate will drive end-to-end project implementation: from equipment design and installation through startup, commissioning, and qualification.

Key Responsibilities:

  • Develop User Requirement Specifications (URS).
  • Lead full validation lifecycle activities: FAT, SAT, CSV, equipment integration, and startup.
  • Drive process design for new equipment and ensure product design requirements are met.
  • Execute commissioning and qualification activities for new and existing equipment.
  • Provide technical oversight to ensure equipment meets safety, regulatory, and operational standards.
  • Manage suppliers and external vendors on capital projects, controlling scope, cost, and lead time.
  • Collaborate with Procurement and Legal on vendor contracts.
  • Create and maintain engineering documentation (URS, assembly instructions, bill of process, etc.).
  • Optimize equipment design for manufacturability, cost reduction, maintainability, and efficiency.
  • Lead design reviews, risk assessments, and FMEA to ensure reliability and performance.
  • Ensure compliance with all safety regulations and quality policies, procedures, and GMP standards.
  • Apply statistical analysis and SPC systems to support data-driven decision-making.
  • Manage multiple priorities and maintain equipment qualification schedules.

Qualifications:

  • Bachelor's degree in Engineering or Science.
  • Minimum 4 years of engineering experience in pharmaceutical and/or medical device industries.
  • Demonstrated experience across the full validation lifecycle (URS, FAT, SAT, CSV).
  • Proven track record supporting full project implementation: design, installation, startup, commissioning, and qualification.
  • Strong experience executing capital projects within GMP-regulated manufacturing environments.
  • Familiarity with GMP, ISO standards, Lean Manufacturing, and FDA-regulated environments.
  • Ability to work independently and lead solutions under general direction.
  • Strong organization, and communication skills

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.