Job details
Job type full-time
Benefits pulled from the full job description
401(k) 401(k) matching dental insurance disability insurance health insurance paid time off show 4 more benefits
Not provided by employer
Full job description
Who are we:
Looking for an exciting opportunity at a fast growing, employee-oriented company? verista’s 500+ experts team up with the world’s most recognizable brands in the life science industry to solve their business needsWhether it’s compliance, quality management, verification, validation, automation, it infrastructure, data analysis, manufacturing, or packaging, we deliver solutions that are right the first time.
Verista’s experts include smes across the spectrum of pharma, medical devices and biotech industriesAs a result, we’re uniquely capable of offering transformative, integrated solutions, new perspectives, and consistent results.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable our clients to improve the quality of patient healthcare worldwideOur talented and dedicated professionals are committed to making an impact every day.
We deliver solutions that are right the first time.
Typical responsibilities include:
Kneat validation engineer this position requires advanced learning; technical precision; and consistent use of independent judgment and discretionKneat validation engineers utilize kneat gx and csv/cqv experience to provide value added solutions to verista clients.
Requirements
Thorough understanding of c&q and/ or csv and the ability to apply and implement this knowledge at a client
Direct experience authoring/editing/executing validation documents
Can demonstrate the functional differences between a paper based system and an electronic system
Kneat expert – process mapping
Master of the 3 kneat elements
Transferring document templates to a work folder
Sharing data across the work process documents
Modifying documents with templatized sections
Ability to translate a work process into the 3 kneat elements
Ability to coordinate teams to complete validation/kneat activities
Requirements
Bachelor’s degree or higher required
3-5+ years’ experience in gmp regulated environment
Ability and willingness to quickly learn new technology
Intermediate knowledge of fda regulations, ispe guidelines and iso standards
Advanced skills with word (authoring/editing large technical documents with styles, template creation, tables, tocs) ·
Capacity to make independent sound decisions and independently manage priorities ·
Proven attention to detail and organization (including technical proofreading, follow-through, and project communication) experienced at effectively communicating to different levels of the organization
Preferred:
Kneat power user 2 or super user certification
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Benefits
Because employees are the key to our success, verista offers strong benefits and incentives including:
Health, dental, and vision insurance
401(k) retirement plan with a company match
Paid time off pay
Tuition reimbursement
9 company paid holidays
Paid long term & short term disability insurance
Training and development
Paid maternity leave and parental leave
Travel bonus
Employee referral program
Tuition reimbursement
Marriage leave
Bereavement
Verista is an equal opportunity employer
Job type: full-time
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Job activity
Posted 30+ days ago
