Client: Leading Medical Device Company. Location: Tempe-AZ, 85281. Contract Term: 4 months with possible extension. Onsite Role. Note: we do not take visa transfers or support sponsorship. This is not a C2C / 1099 role. Top technical skills. 1. Process development (i.e. process characterization and validation – DOE, PCR, TMV, IQ, OQ, PQ). 2. Statistics. Education Required: Advanced degree in Physics, Mechanical Engineering, Materials Science, Che...
Job Description. This role will be heavy on execution and technical writing so just need someone with some familiarity in process validation and who is comfortable learning new equipment and executing. Requirements. BS Degree in Engineering. 2-5 years of experience minimum. Experience in medical device manufacturing is required. Experience in process validation planning, execution and reporting is required. Strong technical writing skills related...
Job Title. Process Validation Engineer. Location: Birmingham, AL. Experience: 3 - 5 Years. Duration: 12 months. Overview. We're looking for a Process Validation Engineer with hands-on experience in aseptic pharmaceutical environments. The role focuses on equipment qualification, facility validation, and computerized system validation activities to support ongoing operations and regulatory compliance. Responsibilities. Aseptic Facility and Equipme...
Job Description As a Process Validation Engineer within the Process Validation team of Agilent Technologies Nucleic Acid Solution Division, the candidate will be responsible for executing process validation activities of oligonucleotide Active Pharmaceutical Ingredient (API) manufacturing. The responsibilities may include: Compile, generate and review process inputs and outputs using statistical process control measures for product quality and pr...
Description. The Process/Validation Engineer is responsible for providing engineering production support including. Implementing process and technology improvements. Process and Cleaning Validation. Equipment Qualification. Collecting, monitoring, analyzing, troubleshooting, and reporting manufacturing data related to performance in the areas of quality, cost, and speed/service to market. Investigating non-conformances, CAPAs, process performance...
Process Validation Engineer - Medical Device Manufacturing. Overview. Seeking a Process Validation Engineer to lead equipment and process validation efforts, ensuring compliance with regulatory and company standards. This role supports product quality, process improvement, and production readiness. Responsibilities. Lead and execute IQ/OQ/PQ protocols for equipment, processes, and systems. Develop and implement validation plans that meet regulato...
The Process/Validation Engineer will be responsible for providing engineering production support, implementing process and technology improvements, and ensuring compliance with regulatory standards. This role involves process and cleaning validation, equipment qualification, change control, and data analysis to drive process efficiency, quality, and compliance. Key Responsibilities. Conduct process and cleaning validation activities and equipment...
