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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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 experience equipment and cleaning / sterilization focused validation expert. With a ...
Job Details. Do you have a passion for precision and a keen eye for detail. Do you thrive in fast-paced environments where ensuring quality is part of the culture. If so, then join our growing team as a Validation Engineer and play a vital role in safeguarding the integrity of our pharmaceutical products. In this role, you'll be responsible for ensuring that our manufacturing equipment and processes consistently meet the strictest cGMP standards....
Job Details. Do you have a passion for Science. Would you like to apply your expertise to impact a company that follows the science and turns ideas into life changing medicines. Then AstraZeneca might be the one for you. . At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, con...
Job Description. Performs cGMP compliance-based services (commissioning, qualification, validation, consulting, etc.) as developed and defined in project agreements with IPS' clients. Follows IPS and client standards and requirements, overall good industry practices for C/Q/V services and regulatory requirements. May also perform standalone commissioning services for non-FDA regulated clients. KEY ACTIVITIES AND RESPONSIBILITIES. Write C/Q/V docu...
Who are we. Technical Safety Services (TSS) is a leading laboratory service provider with locations across the United States. Our customers include leading life sciences and healthcare companies and renowned research institutions. We are rapidly growing and looking for additional passionate and talented employees to join our team and partner with TSS’ customers who are doing dramatic work focused on improving the human condition. TSS ensures the ...
Senior Validation Engineer. COMPI is a full service engineering contracting and consulting services company with a life sciences division specializing in pharma, biotech, API, Medical Device and laboratory facilities. We are seeking an experienced Senior Validation Engineer to join our growing team. COMPI differentiates itself through an integrated approach to engineering, construction commissioning and validation. Responsibilities. . Support Cli...
Senior Validation Engineer. COMPI is a full service engineering contracting and consulting services company with a life sciences division specializing in pharma, biotech, API, Medical Device and laboratory facilities. We are seeking an experienced Senior Validation Engineer to join our growing team. COMPI differentiates itself through an integrated approach to engineering, construction commissioning and validation. Responsibilities. . Support Cli...
PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America...
. We are seeking an experienced Senior Validation Engineer. . Our ideal candidate is a versatile engineering professional, with superior skills and experience in the optimization of procedure improvement and a willingness to work in a dynamic, on-site pharmaceutical project environment. Job Responsibilities. Develop and execute validation/verification protocols for all commercial and R&D manufacturing, processing, and packaging equipment. Analyze...
Title. . Senior Validation Engineer. Overtime Status. . Exempt. Employment Status. . Full-Time. Pay Range. $85,000 - $105,000 /yearly. The hiring pay range for this position is. $85,000 to $105,000. per year based on skills, education, and experience relevant to this role. Inventprise is a mission-driven bio-pharmaceutical company addressing global health inequalities by empowering people to live healthy lives. We do this by developing novel vacc...
General Purpose of Position. . This position is responsible for the execution, tracking, and reporting on Validation and Qualification projects. Validation activities include, but are not limited to, Process Validation, Cleaning Validation, Automation Validation, Computer Validation and Software Validation. This position will also have responsibility for Equipment Qualifications. The role collaborates to develop, maintain, and improve validation ...
Position Description. The CQV Engineer develops documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment. These people are responsible for protocol writing and execution (field verification), and development of summary reports at client sites. Other responsibilities include planning / coordinating work and directing small teams in document development and / or execution. Requirement...
