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...

Our client is a global, research-driven pharmaceutical focusing on treatment options for diseases and conditions for which there is no satisfactory treatment option to date. The company is looking for a Validation Engineer to join the team. This is an amazing opportunity to work on cutting edge treatments and make a difference! Shift : M-F 1st shift Type : 7...

Validation Engineer | Contract-To-Hire Clearwater, FL | On-Site The Validation Engineer is responsible for developing, documenting, and validating manufacturing processes, related to the manufacture, inspection, and packaging of lathed intraocular lenses. Specific tasks to include: new technology and process improvements for existing manufacturing processes,...

Summary of Objective: The Validation Engineer is responsible for the qualification/validation of pharmaceutical equipment, processes, and test methods for the assembly, inspection, testing, and packaging of medical devices. Core functions include management of validation projects, generation and execution of validation protocols, evaluation of statistical...

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...

ADVENT's services include process engineering, automation engineering, project engineering, HVAC/facility system design, process development, start up and commissioning, validation and compliance consulting for distinguished and successful biotechnology and pharmaceutical manufacturing companies. The successful candidate will work with a group of engineers...

Senior Validation Engineer (Contract) Location: Van Nuys Area Role Overview We're seeking a highly skilled Senior Validation Engineer for a temporary onsite role. Reporting to the Manager of Quality Engineering, you'll support our quality engineering team with documentation and validation tasks for automation projects. You'll also draft design...

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...

Not For C2C Candidates Please do not apply even not enquire Job Title: CQV Validation Engineer Location: Countrywide USA Contract Duration: 12+ months Pay: Negotiable on w2 without any benefits Responsibilities: Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and...

Responsibilities: Review qualification requirements for any new instrument, equipment and process with system owner and cross-functional teams. Prepare protocols and reports related to equipment/system/utility qualification (IQ/OQ/PQ), calibrations, engineering, process, packaging, and cleaning validations. Preparation and review of associated procedures,...

Responsibilities: Review qualification requirements for any new instrument, equipment and process with system owner and cross-functional teams. Prepare protocols and reports related to equipment/system/utility qualification (IQ/OQ/PQ), calibrations, engineering, process, packaging, and cleaning validations. Preparation and review of associated procedures,...

Not For C2C Candidates Please do not apply even not enquire Job Title: CQV Validation Engineer Location: Countrywide USA Contract Duration: 12+ months Pay: Negotiable on w2 without any benefits Responsibilities: Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and...

DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES. RECRUITERS: DO NOT CONTACT. SUMMARY OF THE JOB As a Senior Validation Engineer, you will play a critical role in ensuring the quality and compliance of products by developing and implementing robust validation strategies. Your expertise will be essential in verifying and...

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...

*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...

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...