Verista’s 600 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines & Values:
Senior CSV Engineer Responsibilities:
We are seeking a skilled Computer System Validation (CSV) Specialist to support the commissioning and qualification (C&Q) efforts for a cell therapy manufacturing project. This role ensures that computer systems meet regulatory compliance standards and are validated to facilitate product manufacturing.
Responsibilities Include:
Why Choose Verista?
For more information about our company, please visit us at Verista.com
For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.
$70,491-115,000
*Verista is an equal opportunity employer.
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Join Verista as a Senior CSV Engineer/Analyst and be part of a dedicated team where your contributions truly matter! At Verista, we believe in empowering growth and fostering innovation within the life sciences community. As a Senior CSV Engineer, you will play a crucial role in ensuring that computer systems are compliant and validated for a cutting-edge cell therapy manufacturing project. You'll be responsible for developing and executing comprehensive validation protocols, collaborating closely with automation teams, and overseeing necessary documentation to ensure it meets stringent regulatory standards. Working in a fast-paced environment, your analytical skills and attention to detail will help drive the success of critical projects. If you’re passionate about making an impact and want to work within a supportive team that values growth and collaboration, Verista is the perfect place for you! Not only do we provide a competitive salary and benefits, but we also encourage a fun and inclusive culture that respects and engages every team member. Your expertise in Computer System Validation and your experience within a GMP-regulated environment will shine here. If you're looking to advance your career in a place where you can learn and grow, we invite you to apply!
We enable life sciences clients to improve lives.
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