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...

Are you a recent graduate with a degree in Science (Chemical/Biotechnology/Biomedical/Regulatory Affairs), and passionate about a long term career in the Life Science Industry? Validation Associates is the perfect place for you to come to explore what Life Science has to offer. We are looking for people like you to help us continue to thrive. We offer best...

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...

Technical Source is currently in search of a Validation Engineer for our pharmaceutical manufacturing client in Western North Carolina. This is a long-term contract position that requires on-site work. There is a possibility of full-time conversion if internal headcount allows. The qualified candidate should have experience conducting Equipment Validation in...

Title: Validation Engineer Summary: A leading manufacturing company is looking to add a Validation Engineer to their growing team! This is a well-established company with over 50 years of experience in the industry, specializing in manufacturing ingredients used in nutrition products. The Quality Assurance Supervisor will be responsible for: Perform...

Title: Validation EngineerSummary: A leading manufacturing company is looking to add a Validation Engineer to their growing team! This is a well-established company with over 50 years of experience in the industry, specializing in manufacturing ingredients used in nutrition products. The Quality Assurance Supervisor will be responsible for:Perform lab-scale...

Title: Validation Engineer Location: Rapids, MI Duration: 06+ months Key Responsibilities: Validation Strategy Development: Collaborate with clients to develop validation strategies tailored to their specific aseptic manufacturing processes and equipment. Validation Protocol Generation: Lead the development and execution of validation protocols, including...

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...

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 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...

*US Citizens or Greencard Holders only* 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 implementation...

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....