--- title: 'Process Engineer at CAI' canonical: 'https://feeny.ai/job/process-engineer-cai-europe-ireland-yqjz90jpxqd9' type: 'job' last_seen: '2026-09-09' --- # Process Engineer at CAI - **Company:** CAI - **Location:** Europe / Ireland - **Employment:** full-time - **Work type:** onsite - **Posted:** 2024-07-18 - **Last confirmed live:** 2026-09-09 - **Apply:** https://jobs.lever.co/cagents/a06abc53-e13b-42fd-92ba-58b299b78579 ## Job description Process / Commissioning & Qualification (C&Q) Engineer – Biopharmaceuticals ## About CAI CAI is a dynamic, 100% employee-owned company founded in 1996, now encompassing over 800 employees globally. We specialize in Commissioning, Qualification, Validation, start-up, project management, and consulting services across FDA-regulated and other mission-critical industries. Our offices span the United States, Singapore, Australia, Ireland, and across North & South Europe. Learn more at www.commissioningagents.com. Our Commitment to Excellence: At CAI, we prioritize our clients’ success and persist until excellence is achieved. As employee-owners, we uphold our Foundational Principles: Integrity: We act with the utmost integrity. Service: We serve one another, our clients, and society. Sustainability: We work for our future. We believe that individual success drives collective success. Teamwork, respect, and a positive can-do attitude fuel our growth and client satisfaction. Position Overview: We are seeking Senior Process / C&Q Engineers to join our expanding operations, supporting an exciting biopharmaceutical project focused on both upstream and downstream operations. This role involves working with bioreactors (10L to tens of thousands of litres), filtration systems, and other complex equipment, supporting full lifecycle Commissioning & Qualification (C&Q) for GMP drug manufacturing. Responsibilities: Lead conceptual, basic, and detailed design for process equipment and utilities. Support full lifecycle Commissioning & Qualification (C&Q) of complex biopharmaceutical equipment, including bioreactors, filtration skids, tank farms, autoclaves, parts washers, and CIP systems. Author, review, and execute C&Q protocols (IQ/OQ/PQ). Participate actively in all project phases: design, commissioning, qualification, and handover. Collaborate with multi-disciplinary teams, including Process Engineering, Automation, Manufacturing, PDTS, and Validation, to implement improvements and changes. Ensure compliance with applicable EHS requirements, cGMP, and Good Engineering Practices (GEP). Coordinate and manage engineering and construction consultants, equipment vendors, and contractors. Provide process expertise in upstream and downstream bioprocess operations to support equipment design and project implementation. Required Qualifications: Bachelor’s degree in Chemical, Biotechnology, or Biochemical Engineering. 3–5+ years of hands-on experience in downstream bioprocess operations; upstream experience is a plus. Strong background in full lifecycle commissioning & qualification of biopharmaceutical equipment. Demonstrated experience with bioreactors and filtration systems, including protocol writing and execution. Experience supporting cGMP manufacturing operations in pharmaceutical or biotech facilities. Knowledge of PCS7 functional specifications; Siemens PCS7 experience preferred. Knowledge of DeltaV is a plus. Familiarity with design principles, sanitary design, and operation of biopharmaceutical manufacturing equipment. Strong written and verbal communication skills in English. Proficiency with MS Office. Willingness to travel up to 50%. Preferred Experience: Senior-level C&Q engineer background with hands-on execution experience. Exposure to both upstream and downstream processes, especially bioreactors and filtration systems. Proven track record in GMP biotech/pharma projects. ## #LI-JD1 ## About CAI ## Company Overview - **One-liner**: CAI is a global professional services firm that accelerates operational readiness and excellence for life sciences and mission-critical facilities through commissioning, validation, engineering, and digital transformation expertise. - **Entity Type**: Private (Privately Held; raised a venture round in May 2026) - **Headquarters**: Indianapolis, Indiana, United States - **Founded**: 1996 - **Founders**: Not publicly available ## Core Business - **Primary industry/industries**: Life Sciences (pharmaceutical, biotech, medical device manufacturing) and Mission Critical (data centers, high-tech facilities) - **Target customers**: B2B – enterprise-level pharmaceutical companies, biotech firms, data center operators, and regulated manufacturers - **Mission or purpose statement**: “Making what’s next possible” by delivering precision, efficiency, and innovation through commissioning, qualification, validation, and operational readiness services. ## Products & Services For each major offering: - **Commissioning & Qualification (C&Q)**: End-to-end commissioning and qualification services for new and modified facilities, ensuring regulatory compliance and operational readiness. - **Validation Services**: Computer Systems Validation (CSV), cleaning validation, process validation, and equipment validation for life sciences clients. - **Automation & Digital Transformation**: Automation engineering, digital twin solutions, and technology integration to improve facility performance and data integrity. - **Building Commissioning**: Mechanical, electrical, and plumbing commissioning for mission-critical buildings, including data centers and commercial facilities. - **Human Performance & Operational Excellence**: Consulting and training programs to reduce human error, improve safety, and optimize asset management. - **Project Management**: Owner’s project management and full-scale operations support for complex capital projects. ## Market Standing - **Valuation/Market Cap**: Not disclosed (private) - **Key Metric**: Annual Revenue of ~$10.2M (as of latest available data); Total Funding – venture round raised in May 2026 (amount undisclosed, 1 investor) - **Notable Investors/Partners**: One venture investor (May 2026 round); strategic partnerships with technology vendors (unspecified) and participation in industry bodies such as ASHRAE, ASTM, BCA, and ISPE. - **Growth Signals**: - Employee headcount of 562, up 2.6% YoY - LinkedIn followers surged 72.3% over the past year, indicating strong brand interest - 84 active job postings globally - Offices in 5 countries (US, Ireland, Singapore, China, Australia) and operations across 21 countries - Clients include top pharma firms (Pfizer, Eli Lilly, MSD, Novartis, Thermo Fisher Scientific) ## Competitive Advantages - **30 years of deep domain expertise** in highly regulated environments, giving CAI a track record that few competitors can match. - **Elite, credentialed talent** – team members are active in nearly 30 professional societies and help set industry standards (ASHRAE, ISPE, ASTM, BCA). - **Global footprint with local delivery** – ability to support multinational clients across the US, Europe, and Asia-Pacific. - **End-to-end lifecycle support** – from commissioning and validation to digital transformation and operational excellence – reducing handoff risks. - **Strong alumni pipeline to/from top pharma** – CAI attracts talent from Pfizer, Eli Lilly, Bristol Myers Squibb, and others, signaling deep industry credibility. ## Strategic Focus - **Investing in Digital Transformation** – leveraging digital twin technology and automation to drive efficiency for clients. - **Expanding Mission Critical Services** – actively hiring Data Center Commissioning Project Managers and Engineers in the US and Europe. - **Sustainability Integration** – weaving green building practices (LEED, Net Zero Energy) into all client engagements. - **Talent Development** – emphasizing top-tier training and career progression to retain high-knowledge employees. ## Why Work Here - **Culture of teamwork and continuous improvement** – employee testimonials highlight a supportive team environment and commitment to process excellence. - **Global, varied projects** – work on high-impact projects for leading pharma and data center clients across 21 countries. - **Clear career growth** – career/professional development opportunities, exposure to multiple disciplines (validation, automation, commissioning, human performance). - **Benefits package** – comprehensive health insurance, paid time off, competitive 401(k) contribution, income protection, and additional local-region benefits. - **Remote/hybrid/office policy** – roles vary; many positions are client-site based (e.g., commissioning engineers travel to data centers or manufacturing sites). Some office locations available. - **Engineering culture** – strong focus on quality, problem-solving, and precision; ideal for engineers, validation specialists, and project managers who thrive in regulated environments. ## Sources 1. [caiready.com](https://caiready.com/) – Company homepage and about page 2. [caiready.com/about](https://caiready.com/about/) – Company history and mission 3. [caiready.com/careers](https://caiready.com/careers/) – Careers page with benefits and culture 4. [linkedin.com/company/caiconnected](https://linkedin.com/company/caiconnected) – LinkedIn company profile and employee data 5. 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