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Base pay range
$88,000.00 / yr - $121,000.00 / yr
Join a global healthcare manufacturer dedicated to delivering high-quality therapies and technologies that improve outcomes across hospital, clinical, and home settings. Be part of a mission-driven organization focused on patient care and innovation.
About the Opportunity
Our client is seeking a skilled Validation Engineer to support critical system qualifications at a large-scale manufacturing site. This role plays a key part in ensuring that new and existing equipment, software, and facility systems meet industry standards and regulatory requirements.
You'll provide technical validation support for a wide variety of systems—from automated inspection and packaging lines to cleanroom environments and water purification setups. If you enjoy hands-on technical work, process improvement, and collaborating across functional teams, this is a great fit.
What You'll Do
- Lead and support validation activities for facility systems, manufacturing equipment, and automation platforms in compliance with industry regulations and internal policies
- Contribute to equipment and software qualification processes (IQ / OQ / PQ), including development of test plans and execution documentation
- Perform and document validation activities for equipment and processes across a range of systems such as water purification, formulation equipment, automated visual inspection, and lab instruments
- Apply knowledge of regulatory standards (e.g., 21 CFR Part 11, FDA Process Validation Guidance, USP Chapters) to ensure compliance
- Participate in project planning and timeline execution during equipment upgrades, facility shutdowns, and maintenance windows
- Work closely with engineering, IT, QA, manufacturing, and other stakeholders to coordinate validation needs
- Troubleshoot validation-related issues and contribute to root cause analyses, non-conformance resolutions, and change control activities
- Ensure computer system validation (CSV) aligns with software lifecycle protocols and data integrity standards
- Translate technical details into clear documentation and validation reports for internal and regulatory purposes
- Support continuous improvement initiatives and contribute to equipment commissioning as needed
Who You Are
Bachelor's degree in an Engineering discipline (e.g., Mechanical, Electrical, Chemical, Industrial, or Biomedical)At least 3 years of experience in validation engineering or quality assurance within regulated industries such as pharmaceuticals, biotech, or medical devicesExperience with equipment, utility, and computer system validation; familiarity with industry protocols (IQ / OQ / PQ) and data integrity principles (ALCOA)Skilled in interpreting system schematics, protocols, and technical documentationProficient with Microsoft Office applications; experience with tools like AutoCAD, E-Plan, Wonderware, or PLCs (e.g., Allen-Bradley) is a plusSelf-driven with strong problem-solving skills and attention to detailAble to work independently and collaboratively across multi-site or cross-functional teamsExcellent written and verbal communication skillsSalary and Benefits
Salary Range : $88,000 – $121,000 annually (based on location, experience, and qualifications)Additional Benefits Include :Medical, dental, and vision coverage from day one401(k) with company matchStock purchase planPaid parental leave and paid holidaysTuition assistanceGenerous paid time off and sick leavePlease note : This job posting is just a preview of the full scope of the position. A comprehensive job description is shared by a member of our team.
Seniority level
Mid-Senior levelEmployment type
Full-timeJob function
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