Validation Engineer
- Seniority
- Mid-level
- Work
- On-site
- Type
- Full-time
- Degree
- BS
- Experience
- 2+ yrs
- Industry
- General manufacturing
- Role
- Quality / Testing
- Schedule
- Standard
Role details
Validation EngineerThe Validation Engineer will lead validation activities across our production lines. They will have a strong background in quality systems, process validation, and regulatory compliance, with specific experience in plastics manufacturing. This role is critical to ensuring product integrity, customer satisfaction, and continuous improvement. Employee may perform other related duties as required to meet the ongoing needs of the organization.
Essential Responsibilities:
- Develop and implement validation protocols for plastic manufacturing processes primarily focused on NPD.
- Conduct equipment, process, and product validations (IQ/OQ/PQ), ensuring compliance with internal standards and external regulations (ISO 9001).
- Responsible for the following validation documentation: W.I.’s, PFMEA’s, packaging instructions, setup instructions for new parts.
- Be the liaison between process engineering and design engineering to assist with tooling modifications and recommendations.
- Clearly communicate and execute modifications for process engineering to develop new product development.
- Communicate required tooling design changes to the design department for final revision.
- Assist engineering and production teams to improve process capability and product consistency.
- Conduct internal and external audits, including supplier quality assessments.
- Support customer quality requirements, including documentation, reporting, and communication. Manage projects across multiple departments for new and existing tooling needs and modifications.
- Essential Skills:* Bachelor’s degree in; Mechanical, Electro-Mechanical, Manufacturing or Industrial Engineering preferred.
- Minimum 2 years of experience in quality/validation engineering within a manufacturing environment; plastics manufacturing preferred.Strong knowledge of quality standards (ISO 9001).
- Hands-on experience with validation protocols (IQ/OQ/PQ).
- Excellent communication, organizational, and problem-solving skills.
- Proficient in Microsoft Office and QMS software. Knowledge of regulatory standards in medical device or automotive sectors.
- Brentwood offers professional growth potential, a pleasant work environment, and an excellent wage and benefits package including 401K w/employer match. Brentwood Industries, Inc., provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics.
At Brentwood, we have a passion for both our products and our people. Our goal as an employer is to help you excel as an individual and as part of a team by providing you with satisfying, motivating and stimulating work experience. The varied nature of the environment at Brentwood allows you to work alongside industry professionals on a wide range of projects, contributing your knowledge and strengths to develop innovative, market-driven solutions.
To begin the application process, please click the "Apply" button.
Please note: We are not working with external recruiters at this time and are not accepting unsolicited resumes.
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