> Markdown version of [/jobs/ext/4044344-technical-lead](https://www.wearedevelopers.com/jobs/ext/4044344-technical-lead). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Technical Lead - **Company:** HCL Technologies B.V. - **Location:** 'S-GRAVENHAGE, Netherlands - **Experience:** Expert - **Contract:** Permanent contract - **Skills:** Supervisory Control and Data Acquisition (SCADA), Network Planning and Design, Systems Development Life Cycle, Software Engineering, Systems Architecture, System Software, DESIGO Building Automation - **Published:** October 12, 2026 - **Apply:** https://www.indeed.com/viewjob?jk=db41d7df0c9fa8c8 ## About the Role * Strong hands-on experience delivering BAS and EMS systems in regulated (cGMP) manufacturing environments. * Proven experience with Siemens Desigo CC (BAS architecture, PX controllers, graphics). * Proven experience with SIMATIC WinCC / WinCC Unified for EMS / SCADA / data acquisition. * Hands-on Commissioning & Qualification (C&Q) experience, including on-site troubleshooting and fault finding. * Experience developing, reviewing, and governing SDLC and GMP documentation. * Strong understanding of automation networking, I/O, controls, and system architecture. * Experience in maintenance engineering, utilities, facilities engineering, or industrial maintenance. * Experience with utility systems such as HVAC, refrigeration, compressed air, chilled water, boilers, or similar infrastructure. * Ability to work on-site in Boxmeer as part of a project delivery team What you bring to the role * A bachelor's degree in engineering, preferably in Electrical, Mechanical, or Mechatronics Technology, with a minimum of 10 years of relevant experience in an FDA-regulated environment. * Demonstrated experience supporting control systems within a GMP-compliant pharmaceutical manufacturing environment. * A strong track record of successfully executing automation and control system projects in FDA-regulated manufacturing settings. * Foundational knowledge of automation in pharmaceutical or food processing facilities. * Familiarity with industry standards and regulations, including batch control systems, software development life cycle methodologies, 21 CFR Part 11, and GAMP. * Ability to apply cross-disciplinary engineering concepts and practices beyond your primary area of expertise. * Excellent organizational, verbal, and written communication skills, with the ability to effectively engage cross-functional teams and leadership with minimal guidance. * Strong interpersonal skills and a collaborative mindset to thrive in team-based environments. * Working knowledge of programmable logic controllers, industrial controllers, instrumentation, network design, and system software is highly desirable. * Ability to manage multiple priorities and projects simultaneously in a fast-paced environment. * Willingness to participate in rotating after-hours, weekend, and holiday support schedules for emergency troubleshooting and maintenance. * Self-starter with strong attention to detail and the ability to work independently with minimal supervision. * Enthusiasm for working in a dynamic, cross-functional team environment and a commitment to continuous learning and improvement