Validation Engineer

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...

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...

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...

Description: A Validation Engineer plans, implements and monitors the validation strategy in highly regulated industries such as pharmaceutical or medical device manufacturing. This position is onsite in Oceanside. Assignment will go through the end of the year • Lead or support cleaning, equipment, utilities, sterilization and/or autoclave qualification...

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...

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 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...

Our client, a leading medical devices company, is looking for a Verification & Validation Engineer. This is for an initial duration of 12 months and is located in Andover, MA. Top Skills: IEC 60601: Product Safety Standards for Medical Devices 10+ years of experience. 5 years working at a company in the Medical Device Industry. Experience and understands...

Senior Validation EngineerAre 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...

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....

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’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,...

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...

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...

This is a full-time position, and requires a TS/SCI/Full Scope Polygraph Clearance. 2HB Incorporated is seeking a Tempest Engineer in order to support its government customer in Linthicum, MD. As part of our team, you'll get to work on a team of TEMPEST engineers and SMEs helping perform TEMPEST testing and provide TEMPEST engineering recommendations to help...