534 Jobs Found for Pq Swim
Are you ready to take your validation engineering skills to the next level? Join our dynamic team of innovators at Oberg Industries, a leading contract manufacturer specializing in life-changing medical devices. We're seeking a Validation Engineer with a passion for quality, innovation, and the highest standards of excellence.The Validation Enginee...
Job Title: Supplier Quality EngineerJob DescriptionThe Sr. Supplier Quality Engineer will support manufacturing operations such as process validations and line transfer projects. They will also manage suppliers and procurement, working cross functionally with Manufacturing Engineers, Quality Managers, and the Regulatory team.Hard SkillsConducting s...
Key Responsibilities: Validation Protocols: Develop and execute validation protocols (IQ, OQ, PQ) for manufacturing equipment, processes, and software systems to ensure compliance with FDA and ISO regulations. Documentation: Prepare and review validation documentation, including validation plans, test protocols, and final reports, ensuring accur...
The Validation Engineer will be responsible to ensure that validation requirements are met for all existing and new equipment/ facilities/utilities and processes by preparing and executing detailed validation protocols that meet the relevant testing standards and any requirements. Responsibilities: Designs and drafts validation sampling and testing...
Manufacturing Quality Engineer (Contract)
NewPosted 13 Oct 2024a Medical Devices company located in MNManufacturing Engineer (Contract) RESPONSIBILITIES Developing, implementing, and continuously improving manufacturing processes to enhance yield, reduce costs, and improve productivity. Representing Process Engineering in R&D and Project Team meetings, providing technical expertise in technology transfers, analytical method development, validatio...
Responsibilities ● Designs and drafts validation sampling and testing plan/protocols. ● Executes and reports on validation studies such as Process Validation, Cleaning Validation, CSV, Commissioning, IQ, OQ and PQ studies. ● Resolve technical issues encountered during study execution. ● Track and expedite the review and sign-off of quali...
JOB DESCRIPTION Process Validation Design of Experiments Gauge R&R Education Required: Bachelor's degree in technical discipline Years' Experience Required: 4+ Will the contractor be working 40 hours a week? If not, weekly estimate? Yes, 40 hours Does this position require the candidate to be onsite or remote, if hybrid what does the onsite vs remo...
Hi,We are looking for a Manufacturing Process Engineer. Please let me know, if interested. Manufacturing Process Engineer North Haven, CT FT/Contract Participate in Design for Assembly (DFA) / Design for Manufacturing (DFM) activities to verify manufacturability of Product Designs. Actively participate in PFMEA, DFMEA, Process Mapping, and Crit...
Responsibilities: Establish and maintain design history file documentation for development projects (design and development plan, requirements specifications, device master record, IOV matrix, verification, validation summary reports, etc.) Establish and maintain risk management documentation (risk management plan, hazards analyses, failure mode, a...
Career Opportunities with Nova Biomedical Corporation Nova Biomedical is an Equal Opportunity Employer in compliance with Affirmative Action in hiring and promoting women, minorities, veterans, and individuals with disabilities. Nova Biomedical is looking for a Plastics Engineering Intern for the January 2025 cycle in our Lexington Rd, Billerica,...