The Senior Validation Engineer coordinates all validation activities by constant communication with affected departments and personnel; oversees and reviews validation area processes and procedures. Prepares all protocols and reports for validation work. Being a Senior Validation Engineer typically reports to a manager or head of a unit/department. May require a bachelor's degree. Being a Senior Validation Engineer contributes to moderately complex aspects of a project. Work is generally independent and collaborative in nature. Working as a Senior Validation Engineer typically requires 4 to 7 ...years of related experience.More Show Less
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Job Details. Roles & Responsibilities. Develop and execute validation strategies. Lead Process Validation & PPQ activities. Perform C&Q for equipment, utilities, and facility systems. Run risk and gap assessments. Maintain equipment master data and support change controls. Execute floor-level validation in GMP cleanrooms. Coordinate sampling and data collection. Support recipe authoring, data trending, and automation needs. Train and guide cross-...
Job Description. This position is responsible for planning, executing, and documenting commissioning, qualification, and validation (CQV) activities to ensure all systems meet stringent regulatory and client-specific requirements. The Senior Validation Engineer will act as a subject matter expert, collaborating closely with cross-functional teams, including Manufacturing, Facilities, Quality Control and Quality Assurance to deliver robust validat...
Roles & Responsibilities. Develop and execute validation strategies. Lead Process Validation & PPQ activities. Perform C&Q for equipment, utilities, and facility systems. Run risk and gap assessments. Maintain equipment master data and support change controls. Execute floor-level validation in GMP cleanrooms. Coordinate sampling and data collection. Support recipe authoring, data trending, and automation needs. Train and guide cross-functional te...
Roles & Responsibilities. Develop and execute validation strategies. Lead Process Validation & PPQ activities. Perform C&Q for equipment, utilities, and facility systems. Run risk and gap assessments. Maintain equipment master data and support change controls. Execute floor-level validation in GMP cleanrooms. Coordinate sampling and data collection. Support recipe authoring, data trending, and automation needs. Train and guide cross-functional te...
A fast-growing biotechnology company is expanding their team in Salt Lake City, and they are in immediate need of a. Sr. Validation Engineer. to support them fully onsite for. 12 months. The Sr. Validation Engineer will serve as a key contributor to process validation and equipment qualification initiatives, supporting GMP biologics manufacturing. This position is responsible for developing and executing validation strategies, authoring protocols...
Our Mission. Blackrock Neurotech is 100% focused on improving human lives through neuroscience research and technology. The passion and dedication behind this mission has nurtured a dynamic, enjoyable and fulfilling corporate environment in which learning, and growth are commonplace. We operate in an innovative field that requires our staff to meet the highest standards. Every step of the way, we encourage one another by providing continuous moti...
WHAT WE'RE LOOKING FOR. We’re seeking a highly motivated and detail-oriented. Sr. Validation Engineer. to lead and support validation activities across equipment, utilities, and computer systems in a pharmaceutical manufacturing environment. This role is essential to ensuring compliance with cGMP, GLP, and FDA regulations while driving continuous improvement and operational excellence. You’ll collaborate with cross-functional teams, provide techn...
WHAT WE'RE LOOKING FOR. We’re seeking a highly motivated and detail-oriented. Sr. Validation Engineer. to lead and support validation activities across equipment, utilities, and computer systems in a pharmaceutical manufacturing environment. This role is essential to ensuring compliance with cGMP, GLP, and FDA regulations while driving continuous improvement and operational excellence. You’ll collaborate with cross-functional teams, provide techn...
𝙊𝙣𝙡𝙮 𝙒2 – 𝙉𝙤 𝘾2𝘾 / 1099. We are looking for a highly skilled Senior Validation Engineer. to support platform-level electrical and functional validation for next-generation processor and memory subsystems. This role requires strong hands-on experience in memory interface bring-up, FPGA-based validation, and lab-level debugging of high-speed interfaces. This is a. 100% onsite role in Santa Clara, CA. . The project is long-term with strong ...
Sr. Validation Engineer – Wilson, NC (Onsite Only). Long Term Contract. We’re seeking an experienced. Sr. Validation Engineer. to support ongoing commissioning, qualification, and validation activities at a large-scale pharmaceutical manufacturing site in. Wilson, NC. This role requires strong hands-on experience with equipment and automation system qualification, excellent documentation discipline, and the ability to work cross-functionally in a...
. Job Title. Senior Validation Engineer. City. Devens. State. MA. . JOB DESCRIPTION. . Validation. Generate, execute, review, finalize, and approve validation/qualification protocols. Manage and update the validation master plan to align with best industry practices. Assist and deliver amendments to the qualification(s) to ensure qualification compliance within deadlines. Provide validation/qualification support to quality assurance during audits...
Are You Ready. CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For mission-critical and regulated industries that need to deliver critical solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled performance at the highest standard through our rigorous approach, field-tested processes, and elite expertise developed over 30 years. O...
