LABORATORY SUPERVISOR
Versigent designs and delivers the systems that move power through modern technology. From vehicles to robotics to energy platforms, our electrical distribution systems enable the next generation of electrified, automated and connected products.
As a standalone company, we combine deep engineering expertise with the speed and focus needed to solve increasingly complex challenges. Our teams move quickly, think with precision and deliver at scale — helping customers do more without adding cost, weight or complexity.
What defines us is how we work: with the agility and momentum of a startup, backed by the experience and discipline of a proven global leader. That combination creates an environment where ideas move faster, ownership is real and impact is visible.
YOUR ROLE
The EMEA Process Validation Laboratory Supervisor leads all laboratory validation activities across the EMEA region for mechanical, electrical, equipment, and process validations.
This role ensures that validation methods, testing capability, documentation, and compliance are standardized and executed according to Aptiv requirements, customer specifications, and regulatory standards.
Ensure accurate and compliant validation of products, processes, and equipment to support new business launches, customer requirements, and continuous improvement. Promote harmonization and technical excellence in validation across all EMEA sites.
RESPONSIBILITIES
Lead and coordinate Process Validation Laboratory activities across the EMEA region, covering mechanical, electrical, equipment, and process validations.
Manage and develop a regional team of engineers and technicians, ensuring effective workload planning, capability coverage, and performance execution.
Define, standardize, and deploy validation methods, plans, and procedures in alignment with Versigent Global standards and Global Horizontal Teams.
Ensure accurate validation of cables, terminals, connectors, and assemblies to support new product launches and industrialization activities.
Oversee laboratory operations, including testing capacity, scheduling, calibration, equipment maintenance, and resource optimization.
Validate new equipment and manufacturing processes prior to deployment in EMEA manufacturing plants.
Evaluate, approve, and implement new testing methodologies for emerging technologies (e.g. High Voltage, Electrification).
Ensure all validation documentation complies with customer-specific requirements, internal standards, and applicable regulatory frameworks.
Guarantee compliance with Environmental, Occupational Health & Safety, and chemical management standards within laboratory environments.
Act as the regional technical reference during customer audits, technical reviews, and validation-related discussions.
Drive continuous improvement, best‑practice sharing, and digitalization of validation processes across EMEA.
Support and contribute to Six Sigma, ICIM / MCIP / IMCIP initiatives, coaching team members in structured problem‑solving approaches.
YOUR BACKGROUND
Degree in Electrical Engineering, Mechanical Engineering, Materials Engineering, or a related technical field.
5–8 years of experience in manufacturing, validation, test engineering, or quality engineering.
Professional background in an industrial or automotive environment.
Experience working in laboratory or test environments, supporting product or process validation.
Exposure to regional or multi-site operations and cross‑functional collaboration.
Comfortable operating in an international, matrix organization.
Availability to travel up to 50% across EMEA sites and customer locations.
Fluent in English; additional European languages (Portuguese and or French) are an advantage.
QUALIFICATIONS
Proven experience in process, equipment, electrical, and mechanical validation activities.
Hands-on knowledge of cables, terminals, connectors, and wire harness assemblies.
Demonstrated technical leadership or supervisory experience, coordinating engineers and technicians.
Strong understanding of validation planning, execution, and technical documentation.
Familiarity with customer-specific requirements and automotive standards (e.g. VDA, LV standards, OEM CSRs).
Experience with Measurement Systems Analysis (MSA) and equipment qualification (IQ / OQ / PQ).
Working knowledge of Quality Management Systems, ideally IATF 16949 (ISO 17025 is a plus).
Solid understanding of Environmental, Health & Safety requirements, particularly in laboratory environments.
Strong analytical skills with experience applying risk analysis tools such as FMEA and control plans.
WHY JOIN US?
Grow with purpose. We invest in our people by creating opportunities to build skills, take on new challenges, and develop over time.
Do work that shows up in the real world. What you contribute here powers systems that are critical to how industries operate and evolve. The impact is visible and lasting.
Succeed with the right support. We provide the tools, resources, and environment needed to perform at a high level and sustain that success.
YOUR BENEFITS AT VERSIGENT
Private health care effective day 1 of employment
Learning and development opportunities
Recognition for innovation and excellence
Opportunities to give back to the community
Please note that to be considered for this position, candidates must be legally eligible to work in Portugal. This includes having:
Valid residence permit or working visa
Portuguese Tax Identification Number (NIF)
Portuguese Social Security Number (NISS)
Please send your CV in English! APPLY TODAY!
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Versigent is an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, gender identity, sexual orientation, disability status, protected veteran status or any other characteristic protected by law.
