6365 - Senior CQV Engineer / Senior Validation Engineer
External
Veristainc · Devens, MAPrepare for this interview
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About the role
Verista's 500 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: We empower and support our colleagues We commit to client success at every turn We have the courage to do the right thing We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged. We constantly acquire new skills and learn from our experiences to enhance our collective expertise Senior Validation Engineer Responsibilities: Execute IQ/OQ protocols and support operational verification activities Perform Drawing walkdowns (P&IDs, system verification) Perform Equipment/component verification Perform MOC and weld verification Support temperature mapping activities using data loggers and validation tools Assist with SIP/CIP execution and cycle development activities Identify and document deviations and support investigations Ensure accurate and complete documentation in compliance with GMP/GDP standards Work collaboratively with engineering, QA, and operations teams Job Requirements: Bachelor's Degree or equivalent required (STEM degree, Biomedical Engineering, Chemical Engineering preferred) 3-8 years of CQV/validation experience Hands-on experience executing validation for process equipment Strong GMP/GDP fundamentals Experience with IQ/OQ execution and field verification activities Experience with eVal (required), ValGenesis a plus Exposure to temperature mapping (Ellab a plus) Experience with bioprocess equipment preferred (bioreactors, filtration, chromatography, UF) This role requires the ability to be on-site, full-time in Devens, MA. 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. *Verista is an equal opportunity employer. National (US) Range $70,491 - $118,062 USD
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