Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
We are PCI.
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
Summary of Objective:
The Plant Engineer III provides engineering support throughout various manufacturing areas such as process equipment improvements, technological advancements, capital projects, cost improvements, facility maintenance, safety and environmental regulation. Demonstrates good engineering, effective collaboration, partnering and teamwork skills when interacting with internal and external resources. Supports review and approval of the conceptual, basic and detailed design, procurement, installation and start-up for new plants facilities, equipment, utilities and systems. Behaves as a Change Agent to drive innovation and operational effectiveness. Engages with functional department leaders to establish an understanding of the needs/requirements of the department from an equipment capability and capacity perspective. Ensures inclusion of existing site facility and engineering team members in the learning process and design process for new plant systems. Systems include water pretreatment, generation of WFI, plant steam, Clean Steam, Clean Air, Clean Gases, Plant HVAC, Fill Finish equipment and lyophilization. Independently lead Critical and Plant Utility projects from inception to completion.
Essential Duties and Responsibilities:
- Support safety initiatives/ opportunities through personal engagement and promote individual accountability for safety within the Plant Engineering Department. Conduct all activities in accordance with cGMP, EH&S, and the site quality systems.
- Establish and streamline practices around equipment and/or facility specification, design, start-up, and commissioning & qualification. Coordinate design, procurement, installation, engineering start-up, and validation activities of new equipment and systems including documentation of IQ/OQ protocols, executions, and summary reports
- Provide engineer support for Facilities, Systems, Utilities and Equipment (FSUE) execution of projects/assignments from initial concept to final closeout.
- Design and execution of engineering runs to test equipment or to troubleshoot problems.
- Perform process/ equipment investigations and prepare appropriate documentation/ report (deviations, NCs, CAPA).
- Identifies and resolves problems in a timely manner; gathers and analyzes information skillfully; Develops alternative solutions; works well in group problem solving situations. provides the technical support for the user with respect to investigations, re-occurring problems, required modifications, optimizations and Continuous Improvements.
- Work with end users to develop system requirements, specification of equipment/buildings, support fabrication and perform Factory/Site Acceptance Testing.
- Execute good Engineering practices for new equipment/Systems/utilities as applicable.
- Procure new equipment, create and maintain the appropriate engineering records including equipment records and manuals, drawings and diagrams, inspection reports per Good Engineering policies.
Qualifications:
- Bachelor’s degree in Chemical, Mechanical, or other related Engineering or scientific discipline preferred
- 5-7 years’ experience in engineering, facilities clean utilities, preferably in a cGMP environment; equivalent combination of education and experience will be considered
- Strong understanding of technical project management, Good Engineering Practices, reliability, and Lean Principles.
- Experience working in a GMP and FDA regulatory environment for drugs and/or medical devices a plus.
- Strong organization, interpersonal, oral and good written communication skills.
- Demonstrated proficiency in the application of basic manufacturing, engineering, and/or scientific theories, principles, and techniques used in biopharma/medical device processes.
- Proficiency with standard software applications, including Microsoft Office Suite.
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Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future
Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.
Skills Required
- Bachelor’s degree in Chemical Engineering, Mechanical Engineering, or another engineering discipline from an accredited university.
- At least 9 years of engineering, facilities clean utilities, or plant utilities experience.
- Experience in biotechnology, medical device, or pharmaceutical manufacturing.
- Strong understanding of technical project management, Good Engineering Practices, reliability, and Lean Principles.
- Experience with GMP and non-GMP change control and maintaining regulatory compliance.
- Experience with aseptic liquid vial filling, CIP/SIP, cleanrooms, lyophilization, and aseptic processes.
- Experience with CMMS, AutoCAD, SolidWorks, PLC, and SCADA control systems.
- Experience working in GMP and FDA-regulated drug or medical device environments.
- Proficiency applying manufacturing, engineering, and scientific principles to biopharmaceutical or medical device processes.
- Strong organizational, interpersonal, oral, and written communication skills.
- Proficiency with Microsoft Word, Excel, Project, and PowerPoint.
- Knowledge of GMP and FDA regulatory requirements for drugs or medical devices.
PCI Pharma Services Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about PCI Pharma Services and has not been reviewed or approved by PCI Pharma Services.
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Retirement Support — Feedback suggests the company provides a 401(k) with an employer match in the mid‑single‑digit range, with immediate vesting noted in certain cases. This is viewed as a solid component of the overall package.
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Leave & Time Off Breadth — PTO and paid holidays are commonly available, and some roles indicate vacation is accessible from early tenure. Availability of time off is frequently described as a positive element of the package.
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Affordable Benefits — Health insurance is sometimes described as reasonably priced depending on plan tier. Feedback suggests core medical, dental, and vision coverage is part of a standard offering.
PCI Pharma Services Insights
What We Do
PCI is a leading provider of integrated pharmaceutical development services to the global healthcare market. With facilities in North America and Europe, PCI supports pharmaceutical and biotech companies with products destined for more than 100 countries around the world. PCI provides services for each stage of the product lifecycle – from early Phase I through commercial launch and long-term supply – and partners with customers to provide key insight and expertise in enabling successful commercialization and bringing lifesaving medications to patients. For more information, go to www.pci.com.
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