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Equipment Qualification Engineer Job OverviewWe are seeking a detail-oriented and proactive Equipment Qualification Engineer with 3 to 5 years of experience to join our site. This role focuses on managing the qualification lifecycle of GMP production and manufacturing equipment in a small molecule API production facility. The ideal candidate will spearhead new production equipment IQ/OQ executions, lead periodic requalification assessments, and execute mappings for environmentally controlled areas. You will work cross-functionally with Maintenance, Quality Assurance, Engineering, and Production to maintain our facility in a continuous state of compliance.

Key ResponsibilitiesNew Production Equipment IQ/OQProtocol Development & Execution:

Draft, review, and execute Installation Qualification (IQ) and Operational Qualification (OQ) protocols for small molecule processing equipment.

System Field Verification:

Physically verify manufacturing equipment installations against P&IDs, vendor manuals, and site engineering specifications.

Operational Testing:

Evaluate and test production equipment functionality to assure adherence to functional requirements.

Requalification ActivitiesPeriodic Review Cycles:

Perform periodic requalification evaluations of existing production systems to ensure they remain in a validated state.

Deviation Resolution:

Identify, investigate, and document technical deviations or out-of-specification results during qualification executions on the shop floor, authoring robust CAPAs to prevent recurrence.

Environmental Controlled Area MappingExecution & Analysis:

Execute mapping studies for controlled environmental areas, including raw material/finished goods storage areas while also providing support for stability and analytical chambers.

Required Skills & QualificationsEducation:

Bachelors degree in Chemical Engineering, Mechanical Engineering, or a related Life Sciences discipline.

Experience:

35 years of validation or equipment qualification experience. Preferably in a cGMP-regulated pharmaceutical manufacturing environment, with a focus on manufacturing floor equipment.

Collaborative Nature:

Strong project management mindset coupled with the communication skills required to manage cross-functional initiatives across Facilities, Quality, and Operations teams.