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# Reliability Engineer

- **Company:** PCI Pharma Services
- **Location:** San Diego, CA, United States
- **Experience:** Expert
- **Salary:** $106,800.0 - $133,500.0
- **Contract:** Permanent contract
- **Skills:** Data Integrity, Wonderware, Reliability Engineering, DESIGO Building Automation, Allen-Bradley Factory Automation Equipment
- **Published:** October 12, 2026
- **Apply:** https://www.juju.com/job/1_ScrapingHub25741-JR118258

## About the Role

professional mentor for junior colleagues. + Regular and reliable attendance on a full-time basis [or in accordance with posted schedule]. + Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company's policies and practices. + Embodies PCI Pharma Service's cultural values and aligns daily actions with department goals and company culture. + Foster a safe and environmentally sustainable workplace by following all PCI EHS policies and procedures **Qualifications:** + Bachelor's degree in ChE, EE, IE, ME, CS, or similar discipline or equivalent experience required. + Minimum of 7-10+ years of relevant engineering experience including a minimum of 4 years cGMP experience. + Understanding of plant and equipment reliability preferred. + Well-developed understanding of automation standards (including GAMP). + Well-developed understanding of control platforms from
multiple vendors (Allen Bradley, Siemens, Wonderware, iFix, PI). + Extremely strong working knowledge of GMP, aseptic techniques, and laboratory compliance. + Highly proficient in Microsoft Office applications. + Excellent attention to detail, critical thinking, and communication skills. + Able to work autonomously, drive results, and collaborate in a cross-functional environment.

## Description

Our strategy includes building teams across our global network to pioneer and shape the future of PCI. **Essential Duties and Responsibilities:** + Maintain and troubleshoot manufacturing and utility equipment. + Update manufacturing systems. + Provide input and author URS, FDS, SAT, I/O/PQ, and SOP documents. + Document changes to systems per change management procedures. + Research new technologies and make recommendations. + Advanced knowledge of plant and equipment reliability. + Travel between facilities to support all functional areas. + Maintain and troubleshoot automated control systems related to process equipment as well as the Building Management System (Siemens: Insight and Desigo). + Evaluate existing systems for continuous improvement. + Provide in-depth technical review of all documents and complete GMP documentation including change controls, data integrity assessments, deviations and CAPAs, and the closing of audit observations. + Act as a technical and