Senior Inspector QA/QC_BLS

About the role

The Senior Inspector QA/QC is responsible for conducting inspections to ensure that work on a site complies with project design documents, industry pharmaceutical standards, and local, state, and federal building codes in a regulated GMP environment. The role provides technical support to quality engineering (QE) and quality control (QC) functions, captures and analyzes statistical data from processes, and recommends new or enhanced methods, procedures, and standards. Knowledge of high‑tech facility construction, particularly in semiconductor or biopharma environments, is required to maintain safety standards throughout the project.

Responsibilities

• Review Subcontractor Work: Perform and support inspections of MEP, OFCI, and CFCI installations in accordance with ITPs and project specifications; verify workmanship quality, installation compliance, and adherence to approved procedures; support NCR identification, tracking, and closure in coordination with construction teams.
• Code Compliance & Safety: Validate that final installations do not violate code requirements, including equipment clearances, emergency egress paths, and other safety aspects.
• Safety Oversight: Enforce the company safety policy on‑site and ensure continuous compliance with site‑specific safety protocols.
• CQV Interface Coordination: Support coordination with commissioning agents and client representatives during testing and startup activities; participate in system walkdowns and readiness reviews; ensure alignment between construction completion and commissioning sequence requirements.
• Documentation & Reporting: Maintain clear and concise documentation of inspections, audits, and NCRs; ensure reports are completed and submitted on time.
• Perform additional duties as assigned by management to ensure successful project completion.

Requirements

• High School Diploma or GED.
• At least 5 years of experience in pharmaceutical high‑tech facility construction with a strong emphasis on quality assurance and control.
• Proven experience in MEP systems execution in regulated (GMP) environments.
• Proficient in reading and interpreting design documents, building codes, and project specifications.
• Familiarity with OFCI/CFCI equipment integration and turnover processes.
• Preferred: Bachelor’s degree in construction management, engineering, or a related field, or Journeyman Certificate.
• Preferred: Experience in semiconductor or biopharma life sciences facility construction.
• Strong knowledge of biopharma facility construction methods and quality control.
• Experience performing and documenting field inspections to meet quality and regulatory requirements.
• Strong knowledge of relevant building codes, industry standards, and project specifications.
• Proficiency with Microsoft Office Suite, BIM360, and other construction management software.
• Ability to work collaboratively with diverse teams and maintain positive relationships with subcontractors, suppliers, and stakeholders.
• Excellent verbal and written communication skills, with the ability to convey technical information to non‑technical stakeholders.

For questions or further information, contact Clinton Crellin via email at clinton.crellin@exyte.net. Applications are accepted only through the company’s application portal.