Validation Engineer
Company: Eliquent Life Sciences, Inc
Location: New Albany
Posted on: February 15, 2026
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Job Description:
Job Description Job Description ELIQUENT Life Sciences is the
leading global consulting firm providing solutions to life science
companies researching, developing, and manufacturing innovative
products to serve patients and respond to public health challenges
around the world. ELIQUENT is committed to serving clients’ needs
with extensive expertise, unwavering integrity, and strategic
insight in a manner that supports availability of safe, effective,
and high-quality drugs, biologics, and medical devices. For more
information, please visit our website at eliquent.com. We at
Eliquent are looking for an experienced Validation Engineer to
immediately join our Eliquent Consulting: Columbus team. The
Validation Engineer is an FTE project-based role. The Validation
Engineer is responsible for the theory and content of validation
documents for new manufacturing lines, including utilities
qualification, cleanroom qualification, and FAT/SAT/IQ/OQ/PQ of a
new equipment. This will ensure that validation documentation is
compliant with site and corporate validation requirements and
policies as well as compendial (e.g., USP) and regulatory (e.g.,
FDA) expectations/regulations. ESSENTIAL DUTIES AND
RESPONSIBILITIES: Writes procedures, protocols, reports, etc. to
support the Maintenance, Engineering, Validation, Quality, and
Regulatory departments. Generates validation life cycle
documentation (FAT, SAT, IOQ, PQ) for cleaning, sterilization,
facilities, utilities, systems, and equipment
qualification/requalification. Writes and revises a variety of
Installation, Operation and Performance qualification/verification
related documents, including any of all of the following: SOPs,
validation/verification master plans, guidelines and execution
plans, automation test plans, engineering design reviews, user
requirement specifications (URS), functional requirement
specifications(FRS), detailed design specifications, factory
acceptance test documents (FAT), and/or commissioning test
procedures. Performs on site or support work for a client under
supervision, including but not limited to: Validation protocol
execution for FAT/SAT/IQ/OQ/PQ, thermal mapping of
temperature-controlled chambers, warehouses, and sterilization
processes Equipment Qualification test execution Investigations and
deviations Risk analysis, and/or Data integrity assessments and
review of client data Executes protocols and helps resolve
deviations/discrepancies, analyze study data and write summary
reports, under supervision of senior consultants. QUALIFICATIONS
AND REQUIREMENTS: Bachelors Degree in engineering, science, or
similar field or equivalent experience 2-5years experience in
validation services in a regulated, manufacturing environment
within the biotechnology, pharmaceutical, or medical device
industry Experience in executing protocols including systems such
as process validation, utilities, manufacturing equipment and
laboratory validation Experience with temperature mapping Working
knowledge of FDA and cGMP regulations and documentation practice
Ability to read and interpret Piping and Instrument Diagrams
(P&IDs), and electrical diagrams BENEFITS: What We Offer:
Competitive Compensation: Attractive salary and comprehensive
benefits package for full-time and part-time employees, including
health, dental, vision, and life insurance, a 401(k) plan with
employer match, a generous paid time off policy, and additional
perks. Compensation is commensurate with professional experience.
Career Development: Opportunities for professional growth and
advancement within a supportive and innovative environment.
Work-Life Balance: Flexible work arrangements and a commitment to
maintaining a healthy work-life balance. Eliquent Life Sciences is
proud to be an Equal Opportunity Employer, committed to employee
diversity.
Keywords: Eliquent Life Sciences, Inc, Elyria , Validation Engineer, Engineering , New Albany, Ohio
