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 are seeking a highly skilled Commissioning, Qualification, and Validation (CQV) Engineer to join our consulting team. The CQV Engineer will play a crucial role in ensuring the successful commissioning, qualification, and validation of facilities, equipment, and processes in the pharmaceutical, biotechnology, and medical device industries. The ideal candidate will possess strong technical expertise, project management skills, and a thorough understanding of regulatory requirements. Key Responsibilities:
Develop and execute commissioning and qualification protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) of Facilities, Utilities and Equipment (tanks/vessels, centrifuges, filter presses, etc.) Coordinate and oversee the installation, testing, and validation of equipment and systems Ensure compliance with regulatory guidelines (FDA, EMA, etc.) and industry standards (GMP, GxP) Prepare and review validation documentation, including Validation Master Plans (VMP), User Requirement Specifications (URS), and risk assessments Perform validation activities for processes, systems, and equipment, including writing and executing test plans and reports Identify and resolve deviations and non-conformities, ensuring timely corrective actions Communicate effectively with clients, project teams, and stakeholders to ensure project objectives are met Provide technical guidance and mentorship to junior team members Contribute to the development and implementation of best practices and standard operating procedures (SOPs) in CQV activities Stay current with industry trends, technological advancements, and regulatory changes Requirements Lead and execute validation activities for lyophilizers, including cycle development, qualification (IQ/OQ/PQ), and performance monitoring. Support validation and qualification of fill‑finish equipment, such as filling lines, isolators/RABS, cappers, and associated utilities. Plan, coordinate, and execute media fill (aseptic process simulation) activities in compliance with regulatory expectations. Develop and author validation protocols, reports, risk assessments, and supporting documentation. Partner with Manufacturing, Quality, Engineering, and Technical Operations to ensure validated state of equipment and processes. Troubleshoot validation deviations, perform root‑cause analysis, and implement corrective/preventive actions (CAPA). Maintain compliance with FDA, EMA, and global GMP requirements related to aseptic processing and equipment validation. Support change controls, equipment upgrades, and continuous improvement initiatives. Ensure validation activities are executed safely, on schedule, and aligned with project timelines. 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.
