Validation Engineer

Not for C2C Candidates Please Role: All Validation Engineer (V&V, CQV, CSV, Equipment, Process) Location: Country Wide USA Duration: 12+ months + extensions Visa{ USC, GC, H4 OPT CPT Job Description: Process and equipment qualification (IQ/OQ/PQ). Development of test methods for Design V&V, Process Validation, and Production Validation of test...

Title: Validation Engineer III, Req#: ROCGJP00025890 Location: Oceanside, CA (100% onsite) Duration: 8+ months Contract Job Description: A Validation Engineer plans, implements, and monitors the validation strategy in highly regulated industries such as pharmaceutical or medical device manufacturing. Education and Experience: 5 -7 years of relevant...

Senior Validation Engineer RESPONSIBILITIES Leading start-up, commissioning, qualification, validation and revalidation projects for facility, equipment, critical utility, automation/computer system, cleaning, sterilization, medical device, and drug product manufacturing processes. Leading the delivery of validation within complex, capital projects...

*US Citizens or Greencard Holders only* **No C2C** Work Schedule: Onsite - M-F Salary: $60-70/hr Duration: 4 months Primary Responsibilities: Support the Quality Engineering group with documentation and validation needs. Draft URS documents, design specifications, testing protocols, and final reports. Perform hands on validation execution for automation...

Senior Validation Engineer Are you a validation expert looking for a new, dynamic environment? I am partnering with a rapidly growing full service CDMO who are specialised within sterile product development, manufacturing and packaging, and am working with the leadership team to help appoint a number of new hires. For this specific hire, we are seeking and...

Join Our Team as a Validation Engineer Are you ready to make a significant impact in the cloud networking industry? Our client, a premier cloud networking company, is seeking a talented Validation Engineer to join their Electrical Design Validation Testing (EDVT) team. As a Validation Engineer, you will play a crucial role in ensuring the functionality of...

Key Responsibilities Strong Experience in Computer Systems Validation (CSV) within the pharmaceutical industry. Required Bachelor's degree in pharmaceutical Science OR related field of study. Schedule and plan equipment and process qualification workload to meet approved schedules. Handle multiple projects and be able to work independently as required....

Job Title: - CAN Validation Engineer Job Location: - Foster City, CA (On-Site) Employment type: - 12+ Months contract Responsibilities in this role include: Analyses the ECU and provide the diagnosis report to other team members such as the developer and Testers Work on CAN Network Design and analysis Build a CAN Network report database Requirements: Review...

We are looking for a: Mechanical Development and Validation Engineer The resource will be involved in: Coordinating bench testing with nominated suppliers to fully execute Design Validation Plans activities within the required timeframe Working with testing suppliers for debugging and triage of on-going test issues (at the plant or on the...

We’re ALTEN Technology USA, an engineering company that provides solutions for engineering, technology, and product development projects. For decades, we’ve been helping our clients develop products that are changing the world, whether that’s by shaping the future of space exploration, saving lives with medical devices that set a new standard of care,...

Come Innovate MedTech with us! The Senior Quality Engineer for Vandalia, OH., will support all aspects of the Quality Assurance (QA) program within the Quality Management System (QMS). The QE reports to the Q&R Manager. This position will lead all customer and third-party quality audits. Participate in Design Project Teams as a QE/QA Representative to ensure...

Facilities Validation Engineer No C2C or sponsorship The Validation Engineer is responsible for completing assigned equipment validation, packaging validation, computers validation, cleaning validation, and process areas to meet cGMP requirements. Job Function: Prepare and execute IQ / OQ / PQ protocols and write summary reports for production/packaging...

One of our large pharmaceutical clients is actively looking for a Validation Senior Specialist, specializing in Filter Validation, to join their team in West Point, PA. The Validation SME will be responsible for oversight of validation activities as part of the Bio-Sterile Validation SME Team. Main responsibilities include change control assessments for...

Facilities Validation Engineer No C2C or sponsorship The Validation Engineer is responsible for completing assigned equipment validation, packaging validation, computers validation, cleaning validation, and process areas to meet cGMP requirements. Job Function: Prepare and execute IQ / OQ / PQ protocols and write summary reports for production/packaging...

Facilities Validation Engineer No C2C or sponsorshipThe Validation Engineer is responsible for completing assigned equipment validation, packaging validation, computers validation, cleaning validation, and process areas to meet cGMP requirements. Job Function: Prepare and execute IQ / OQ / PQ protocols and write summary reports for production/packaging...

Facilities Validation Engineer No C2C or sponsorshipThe Validation Engineer is responsible for completing assigned equipment validation, packaging validation, computers validation, cleaning validation, and process areas to meet cGMP requirements. Job Function: Prepare and execute IQ / OQ / PQ protocols and write summary reports for production/packaging...

Facilities Validation Engineer No C2C or sponsorship The Validation Engineer is responsible for completing assigned equipment validation, packaging validation, computers validation, cleaning validation, and process areas to meet cGMP requirements. Job Function: Prepare and execute IQ / OQ / PQ protocols and write summary reports for production/packaging...

Job DescriptionJob DescriptionValidation & 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...

Must Have: 1. cleaning validation experience 2. strong communication skills 3. ability to manage, execute and troubleshoot on their own 4. Strong Microsoft Suite skills Roles and Responsibilities Experience in cleaning validation in the biologics or vaccine industry to include the following: o Experience in authoring, reviewing, executing and approving...

Quality Chemical Laboratories (QCL), a leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of Validation Engineer. This position, in the Manufacturing and Formulations Services department, requires a Bachelor’s degree or higher in a scientific or engineering discipline with either 3...