CQV

Job in Boston, Suffolk County, Massachusetts, 02108, USA

Listing for: Kasmo Global

Full Time position
Listed on 2026-07-01

Job specializations:

Engineering
Validation Engineer, Pharma Engineer, Quality Engineering

Pharmaceutical CQV Engineer

A major pharmaceutical company in Los Angeles is seeking a CQV Engineer for an onsite position supporting facility and equipment commissioning and qualification. This role focuses on supporting capital projects through lifecycle documentation, equipment validation, and daily job walks on an active construction site.

Key Responsibilities

Develop and execute CQV documentation (URS, FS, DS, SOPs, MOC, Risk Assessments, Protocols)
Perform IQ/OQ/PQ for equipment such as centrifuges, filter presses, and tanks
Support installation, commissioning, and start-up activities
Conduct job walks, safety reviews, and construction oversight
Execute process, cleaning, and facility validation protocols
Train personnel and maintain validation records
Participate in change control, audits, and deviation resolution

Requirements

Bachelor's degree in Engineering or related field
2–4 years of validation experience in pharmaceutical manufacturing
Experience with EMPO, Vessel IOV/IOPQ, temp mapping, and technical documentation
Strong communication and cross-functional coordination skills
Ability to work independently and manage multiple tasks
Willingness to commit to a long-term project (up to 2 years)

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