32.524 Ofertas de Administración Pública en España

¿Eres un/a ingeniero/a con experiencia en certificación, cumplimiento normativo o gestión de proyectos técnicos? ¿Te gusta trabajar con clientes, normas y equipos de ensayo para facilitar la comercialización de productos en los distintos mercados? Si es así, nos gustaría conocerte.
Como Ingeniero/a de Proyectos de Certificación con sede en Getafe, Madrid (España), usted gestionarás proyectos de certificación de principio a fin, coordinando evaluaciones técnicas, actividades de ensayo y entregables de certificación. Actuarás como principal punto de contacto entre clientes, laboratorios, equipos de certificación y otras partes interesadas, garantizando que los proyectos se ejecuten en plazo y conforme a los requisitos aplicables.
Además, darás soporte a auditorías internas y externas, contribuyendo a mantener la preparación para acreditaciones y la mejora continua de los procesos de certificación.
Responsabilidades
+ Gestionar proyectos de certificación, incluyendo la definición del alcance, la planificación, los entregables y la comunicación con clientes.
+ Coordinar actividades de ensayo, revisiones técnicas y procesos de certificación con equipos internos y externos.
+ Revisar documentación técnica e informes de ensayo conforme a las normas y requisitos de certificación aplicables.
+ Apoyar la resolución de incidencias técnicas y no conformidades identificadas durante la ejecución de los proyectos.
+ Preparar y mantener la documentación asociada a los proyectos y procesos de certificación.
+ Dar soporte en auditorías internas, evaluaciones externas y actividades de acreditación.
+ Colaborar en la gestión de acciones correctivas y preventivas derivadas de auditorías.
+ Participar en iniciativas de mejora continua orientadas a la calidad, la eficiencia y la satisfacción del cliente.
+ Realizar desplazamientos cuando sea necesario para apoyar actividades de certificación, ensayos y auditorías.
Requisitos
Imprescindibles:
+ Titulación universitaria en Ingeniería Eléctrica, Ingeniería Industrial, Ingeniería de la Energía o disciplina técnica afín.
+ Conocimiento de la norma ISO/IEC 17025 y de procesos de acreditación.
+ Experiencia en la gestión de proyectos técnicos o de certificación.
+ Capacidad de organización, comunicación y resolución de problemas.
+ Habilidad para gestionar múltiples proyectos y partes interesadas de forma simultánea.
+ Nivel fluido de inglés.
Valorables:
+ Experiencia en entornos de ensayo, inspección, certificación o evaluación de la conformidad.
+ Conocimiento de esquemas de certificación y requisitos regulatorios.
+ Experiencia dando soporte a auditorías internas o externas.
+ Conocimiento de la norma ISO/IEC 17065.
En UL Solutions, estamos comprometidos con el fomento de una cultura laboral que valore y promueva la igualdad de oportunidades para todas las personas empleadas, independientemente de su género. Creemos que la diversidad y la inclusión son fundamentales para nuestro éxito e innovación, y trabajamos activamente para garantizar que mujeres y hombres tengan el mismo acceso a oportunidades, recursos y desarrollo profesional.
#LI-SB1
UL LLC has been and will continue to be an equal opportunity employer. To assure full implementation of this equal employment policy, we will take steps to assure that:
Persons are recruited, hired, assigned and promoted without regard to race, color, age, sex or gender, sexual orientation, gender identity, gender expression, transgender status, religion, creed, national origin, ethnicity, citizenship, ancestry, disability, genetic information, military or veteran status, pregnancy, marital or familial status, or any other protected category under applicable law.

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.
The Level VI Production Operator (Technician IV) executes, runs autonomously, advises and leads complexs activities of aseptic manufacturing of batches, billable activities, or continuous improvement activities required in the production department, following instructions and standard operating procedures in accordance with the AEMPS, FDA, and other regulatory agencies under supervision. In addition, they must ensure the execution of production plans, following all company safety guidelines. A high level of detail is required due to the complexity of the activities to be performed. The minimum training time for this is normally 5 years.
· Comply with manufacturing area safety regulations and work practices in accordance with all company health, safety and environmental programs.
· Work as a team, being approachable, practical, motivating, able to support and inspire your co-workers.
· Comply with the schedule by following the prioritization instructions of their senior managers to ensure compliance with the schedules together with the department head.
· Collaborate in the identification of opportunities for continuous improvement to improve processes and practices.
· Comply with the requirements of cGMP, AEMPS, FDA and other regulatory agencies that have been implemented in the plant, as well as with the department's objectives and corporate quality standards.
· Collaborate and participate in preparing for inspections by regulatory agencies or clients.
· Participate in the control of the stock of plant consumables, to guarantee their availability.
· Collaborate in the investigations of the different quality events (deviations, capas, change controls.).
· Inform the direct manager when anomalies are detected in the operation of equipment, as well as human errors, both their own and those of the team's personnel, to ensure the quality of the product manufactured.
· Inform the direct manager if safety equipment or human resources needs are identified.
· Collaborate in teamwork with other departments if required.
· Take care of and ensure the proper functioning of the equipment.
· Operate production equipment following the guidelines indicated in the work procedures.
· Participate in the manufacture of the different products following the indications of the manufacturing guides and complying with cGMP regulations.
· Handle pallet trucks for the movement of goods.
· Review relevant sops and production lot records, as needed.
· Complete and maintain documentation related to assigned work, including notebooks, batch records, etc
· Comply with and maintain cleanliness and order of production areas in accordance with appropriate standard operating procedures.
· Operate production equipment following the guidelines indicated in the work procedures
· Supports the manufacture of the different products following the instructions of the manufacturing guides and complying with cGMP regulations.
· Supports the activities of the qualification of production equipments.
· Demonstrate a general knowledge of aseptic techniques (maintaining difficult body posture and movement during long periods of time).
· Successful participation in the gowning qualification as well as the media fill plan.
· Leads the activities of dispensing and preparing materials to be used in the activities of the department.
· Perform the sanitization of materials prior to their introduction into the manufacturing areas.
· Disinfect classified and non classifies clean production rooms.
· Leads the activities of set up grade D/C ( ex. activities of the processes of preparation of autoclave cycles and assembly of installations, perform cleaning of production equipment.).
· Leads the activities of set up grade A/B
· Leads the activities of formulation processes grade C.
· Leads the activities of formulation processes grade A/B.
· Leads the activities of the activities of filtration processes grade C.
· Leads of the activities of filtration processes grade AB.
· Leads filling activities.
· Leads the activities of sip execution of sterilizable equipment.
· Leads the activities of sip execution of complex sterilizable equipment.
· Trains technicians level III
· Shift supervisor back-up
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future ( 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._
Why work for PCI Pharma Services?
At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.
PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled

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.
The Level VI Production Operator (Technician IV) executes, runs autonomously, advises and leads complexs activities of aseptic manufacturing of batches, billable activities, or continuous improvement activities required in the production department, following instructions and standard operating procedures in accordance with the AEMPS, FDA, and other regulatory agencies under supervision. In addition, they must ensure the execution of production plans, following all company safety guidelines. A high level of detail is required due to the complexity of the activities to be performed. The minimum training time for this is normally 5 years.
· Comply with manufacturing area safety regulations and work practices in accordance with all company health, safety and environmental programs.
· Work as a team, being approachable, practical, motivating, able to support and inspire your co-workers.
· Comply with the schedule by following the prioritization instructions of their senior managers to ensure compliance with the schedules together with the department head.
· Collaborate in the identification of opportunities for continuous improvement to improve processes and practices.
· Comply with the requirements of cGMP, AEMPS, FDA and other regulatory agencies that have been implemented in the plant, as well as with the department's objectives and corporate quality standards.
· Collaborate and participate in preparing for inspections by regulatory agencies or clients.
· Participate in the control of the stock of plant consumables, to guarantee their availability.
· Collaborate in the investigations of the different quality events (deviations, capas, change controls.).
· Inform the direct manager when anomalies are detected in the operation of equipment, as well as human errors, both their own and those of the team's personnel, to ensure the quality of the product manufactured.
· Inform the direct manager if safety equipment or human resources needs are identified.
· Collaborate in teamwork with other departments if required.
· Take care of and ensure the proper functioning of the equipment.
· Operate production equipment following the guidelines indicated in the work procedures.
· Participate in the manufacture of the different products following the indications of the manufacturing guides and complying with cGMP regulations.
· Handle pallet trucks for the movement of goods.
· Review relevant sops and production lot records, as needed.
· Complete and maintain documentation related to assigned work, including notebooks, batch records, etc
· Comply with and maintain cleanliness and order of production areas in accordance with appropriate standard operating procedures.
· Operate production equipment following the guidelines indicated in the work procedures
· Supports the manufacture of the different products following the instructions of the manufacturing guides and complying with cGMP regulations.
· Supports the activities of the qualification of production equipments.
· Demonstrate a general knowledge of aseptic techniques (maintaining difficult body posture and movement during long periods of time).
· Successful participation in the gowning qualification as well as the media fill plan.
· Leads the activities of dispensing and preparing materials to be used in the activities of the department.
· Perform the sanitization of materials prior to their introduction into the manufacturing areas.
· Disinfect classified and non classifies clean production rooms.
· Leads the activities of set up grade D/C ( ex. activities of the processes of preparation of autoclave cycles and assembly of installations, perform cleaning of production equipment.).
· Leads the activities of set up grade A/B
· Leads the activities of formulation processes grade C.
· Leads the activities of formulation processes grade A/B.
· Leads the activities of the activities of filtration processes grade C.
· Leads of the activities of filtration processes grade AB.
· Leads filling activities.
· Leads the activities of sip execution of sterilizable equipment.
· Leads the activities of sip execution of complex sterilizable equipment.
· Trains technicians level III
· Shift supervisor back-up
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future ( 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._
Why work for PCI Pharma Services?
At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.
PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled

Xylem is a Fortune 500 global water solutions company dedicated to advancing sustainable impact and empowering the people who make water work every day. As a leading water technology company with 23,000 employees operating in over 150 countries, Xylem is at the forefront of addressing the world's most critical water challenges. We invite passionate individuals to join our team, dedicated to exceeding customer expectations through innovative and sustainable solutions.
Como parte de nuestro crecimiento continuo, buscamos un/a **Sales Engineer, Treatment Aquatics - Madrid** con experiencia para apoyar iniciativas estratégicas y reforzar nuestras capacidades de ejecución de proyectos.
**El puesto:**
Como **Sales Engineer - Treatment Aquatics** , serás responsable de desarrollar el mercado de las soluciones de tratamiento para instalaciones acuáticas de Xylem, con foco en piscinas públicas, municipios y socios de ingeniería. Participarás activamente en la captación de nuevos clientes, la construcción de relaciones estratégicas y la expansión de la presencia de Xylem en el mercado ibérico.
**Responsabilidades principales:**
+ Impulsar el desarrollo de negocio y el crecimiento de ventas de soluciones de tratamiento de agua para instalaciones acuáticas en España y Portugal
+ Identificar y captar nuevos clientes en el sector de las piscinas públicas
+ Desarrollar relaciones con municipios, ingenierías consultoras y operadores de piscinas
+ Promover las soluciones de Xylem, incluidos sistemas de desinfección, bombas y tecnologías de monitorización y control
+ Realizar seguimiento de las tendencias del mercado y de las actividades de la competencia
+ Representar a Xylem en eventos del sector, ferias y reuniones con clientes en España
+ Proporcionar soporte back-office
+ Liderar negociaciones y cerrar contratos de venta
+ Mantener y gestionar oportunidades en el sistema CRM
+ Facilitar previsiones mensuales y actualizaciones del pipeline comercial
**Requisitos:**
+ Titulación en Ingeniería, Tecnología Ambiental, Tecnología del Agua o una disciplina técnica relacionada
+ Experiencia en ventas técnicas, ingeniería de aplicaciones o desarrollo de negocio
+ Sólido conocimiento de tecnologías de tratamiento de agua, bombas o sistemas acuáticos
+ Experiencia trabajando con clientes municipales o en proyectos de infraestructuras públicas
+ Excelentes habilidades de comunicación y de creación de relaciones profesionales
+ Fuerte orientación comercial, con capacidad para desarrollar nuevos mercados y clientes
+ Experiencia en el uso de sistemas CRM para la gestión comercial
+ Español e inglés fluidos (el portugués será un plus)
+ Disponibilidad para viajar un **50 % o más** dentro de España y Portugal
**Location:** España
**Benefits:** Seguro Medico y Seguro de vida
Join the global Xylem team to be a part of innovative technology solutions transforming water usage, conservation, and re-use. Our products impact public utilities, industrial sectors, residential areas, and commercial buildings, with a commitment to providing smart metering, network technologies, and advanced analytics for water, electric, and gas utilities. Partner with us in creating a world where water challenges are met with ingenuity and dedication; where we recognize the power of inclusion and belonging in driving innovation and allowing us to compete more effectively around the world.

**Join the Future of Sustainability at Solstice Advanced Materials**
At Solstice (Nasdaq "SOLS"), we focus on advancing innovation to improve what matters most to our Customers and to Society. Marketed under the Solstice® brand, our extensive range of refrigerants, propellant and blowing agent solutions enable eco-efficient, sustainable and decarbonized heating and cooling, high-performance insulation for buildings and cold chain infrastructure, and aerosol medication.
**Unleash Your Potential as Senior Business Development Manager in Commercial Refrigeration**
An exceptional and exciting career opportunity awaits you as a Senior Business Development Manager to be the driving force of transformation in Commercial Refrigeration and Cold Chain applications.
In this role, your mission is to identify, nurture and win growth opportunities with end-users and system operators in Food Retail, Food Service and Cold Chain, generating demand for our high-performance and eco-efficient Solstice® solutions for refrigeration, cooling and heating systems. You will engage with executives making decisions on refrigeration and HVAC infrastructure, and strategically leverage Solstice's compelling value propositions, centered on sustainability, energy efficiency, operational resilience, and total cost of ownership. Other key influencers in this ecosystem will be OEMs and wholesalers supplying commercial refrigeration equipment and components, engineering consultants, refrigeration contractors and installers. You will drive the development of new business models and breakthrough initiatives.
Reporting to the Sales & Business Development Leader OEM & Food Retail Europe, the role will cover Southern Europe (Spain, Italy, Portugal, Greece, Cyprus, Malta and the Balkan area) and be based out of Spain.
**Responsibilities**
**Key Responsibilities:**
+ Identify new customer and project opportunities that will drive growth for Solstice® sustainable refrigerant solutions in the Commercial Refrigeration and Cold Chain applications (Food Retail, Food Service, Cold Storage).
+ Create senior level & C-suite engagement with key end-users, OEMs, consultants, contractors and installers, and forge strategic partnerships in the value chain for mutual growth.
+ Educate market stakeholders on regulations which are currently, and potentially in future, impacting their business and their operations.
+ Drive customer projects from inception to closure with a sense of urgency; collaborate internally with Sales, Technical and Marketing teams.
+ Develop a robust opportunity pipeline aligned with our strategic goals, and implement structured account plans for your main market stakeholders.
+ Manage accurately & timely your sales opportunity pipeline in SFDC (salesforce.com) and meet the Sales Excellence metrics.
+ Contribute to revenue generation in your territory to meet or exceed sales & profitability targets as per our AOP (annual operating plan) and NPI/BTI (New Product Introduction / Breakthrough Initiatives) targets.
+ Collect and share market and competitor intelligence across the value chain.
+ Participate in relevant industry associations, trade events and meetings and engage stakeholders to promote Solstice® sustainable refrigerant solutions.
**Qualifications**
**You Must Have:**
+ **A pioneer and hunter mentality, tenacity, and a resilient mindset, able to positively deal with adversity and overcome challenges.**
+ >10 years of B2B sales and/or business development experience in a multinational context.
+ Spoken and written Spanish and English is essential; the ability to speak Italian or other European languages is advantageous.
+ Strong Customer focus, ability to understand and clearly articulate value propositions, to analyze customers' needs and use consultative selling skills to solve problems and create customer value.
+ Strong networking, influencing, negotiating and closing skills, paired with sharp organization & project management skills.
+ Commercial and financial acumen - ability to understand CapEx, OpEx, Return on Investment, Total Cost of Ownership concepts.
+ Excellent presentation & written communication, and interpersonal skills.
+ Readiness to travel frequently (40-50%).
**We Value:**
+ Experience in selling value-based Commercial Refrigeration solutions into the Food retail, Food Service and Cold Chain ecosystems.
+ Experience in dealing with regulated products and with political/policy topics impacting business.
+ Adaptability and the ability to move from the strategic to the tactical as the situation dictates.
+ Ability to work collaboratively in a diverse cultural team and in a matrix environment.
+ Ability to take initiative and work with limited direction.
+ Ability to influence across a broader organization.
+ Ability to work remotely.
**Join Our Inclusive Community**
_We are an equal opportunity employer and value diversity within our company. We do not discriminate against anyone based on ethnicity, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability._
_We ensure that individuals with disabilities are provided reasonable accommodations to participate in the application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation._
**About Us**
**About Solstice Advanced Materials**
Solstice Advanced Materials is a leading global specialty materials company that advances science for smarter outcomes. Solstice offers high-performance solutions that enable critical industries and applications, including refrigerants, semiconductor manufacturing, data center cooling, nuclear power, protective fibers, healthcare packaging and more. Solstice is recognized for developing next-generation materials through some of the industry's most renowned brands such as Solstice®, Genetron®, Aclar®, Spectra®, Fluka, and Hydranal. Partnering with over 3,000 customers across more than 120 countries and territories and supported by a robust portfolio of over 5,700 patents, Solstice's approximately 4,000 employees worldwide drive innovation in materials science. For more information, visit Advanced Materials ( .
**Job Identification**
**Job Category** Sales
**Job Schedule** Full time
**Locations** c/o Ernst & Abogados, S.L.P., Torre Azca, c/ Raimundo Fernandez Villaverde, number 65, Madrid, Comunidad de Madrid, 28003, ES
**Hire Eligibility** Internal and External
**Relocation Package** None

Be a part of our mission! As a world leader in creating comfortable, sustainable, and efficient climate solutions for buildings, homes and transportation, it's our responsibility to put the planet first. For us at Trane Technologies ( , and through our businesses including Trane® ( and Thermo King ( , sustainability is not just how we do business-it is our business. Do you dare to look at the world's challenges and see impactful possibilities? Do you want to contribute to making a better future? If the answer is yes, we invite you to consider joining us in boldly challenging what's possible for a sustainable world.
Learn about our benefits ( designed for you to Thrive at work and at home.
We boldly go.
**Where is the work:**
On-Site (5 days)
We offer competitive compensation and comprehensive benefits and programs. We are an equal opportunity employer; all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, pregnancy, age, marital status, disability, status as a protected veteran, or any legally protected status.

**Be visionary**
Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.
We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins.
**Job Description**
**About us**
You may not realize it, but Teledyne enables many of the products and services you use every day. Teledyne provides enabling technologies to sense, transmit and analyze information for industrial growth markets, including aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research.
Teledyne e2v is recruiting a **Package Design Engineer,** this position can be based at our Saint‑Egrève site (near Grenoble, France) or at Teledyne Anafocus in Seville (Spain).
**Teledyne e2v Semiconductors SAS,** **based in Saint‑Egrève** **(near Grenoble),** has been a recognized semiconductor specialist for more than 70 years. Our 400‑employee site brings together research and development teams, production workshops, and support functions for two main business areas:
+ Machine Vision Sensors (MVS) for image sensors, dental sensors, and cameras.
+ High-Performance and High-Reliability semiconductor products: microprocessors, memories and high‑speed data converters.
**Teledyne Anafocus, located in the Seville Tech Park,** is a center of excellence in CMOS image sensor and vision‑on‑chip design, with a highly skilled engineering team and a strong innovation culture. Now fully integrated within Teledyne e2v, the site develops next‑generation imaging technologies for industrial, scientific, medical and surveillance applications.
**Job description**
The Package Design Engineer leads the complete design flow of advanced microelectronic packages-translating customer needs into technical specifications, defining the solution, and ensuring successful routing and design reviews.
As the key technical interface, the Package Design Engineer works closely with packaging vendors and assembly houses throughout the project lifecycle. The role also involves monitoring emerging technologies and leading R&D or continuous‑improvement initiatives to shape future generations of imaging packages.
**What You'll Do**
Management of the full design flow of organic and ceramic multi-layers microelectronics packaging (BGA, PGA, CLCC, CQFP, WLCSP):
+ Identify customers' needs.
+ Devise a solution and a specification.
+ Interact with packaging manufacturers to obtain a solution and a quote all along the design process.
+ Interacting with project teams (sensor designers, project manager.)
+ Implement the design + routing of the package in accordance with the constraints and timing as originally defined.
+ Conduct, electrical, thermal and mechanical simulations when necessary.
+ Conduct DRC checks in accordance with e2v methodologies.
+ Conduct different design reviews including the final one before ordering the package.
+ Assume the role of design expert with respect to assembly houses (assembly instructions.)
Ensure technical interface with package vendors and assembly houses:
+ Guide technical reviews with package vendors.
+ Technical Identification and evaluation of new vendors.
Technology monitoring :
+ Maintain a technology watch on future generations of imaging packages.
+ Identify and lead R&D or continuous improvement projects on these technologies.
**Why Join Us**
A strong customer focused individual (active listening and customers satisfaction), team-worker, with ability to adapt and communicate on subjects requiring rigor.
Autonomy to plan for results & continuous improvement are necessary qualities for this position
**What You Need to be successful in this role**
+ Background in microelectronics, in electronics (preferred), material science or micromechanics
+ First confirmed experience in packaging design.
+ Specific experience in imaging and/or assembly would be a serious plus.
+ Mastering of package design flow: specification, identifying solutions, design, validation.
+ Mastering packaging layout meeting signal/power integrity aspects (under Cadence APD or equivalent).
+ Knowledge basic mechanical design (Solid works or equivalent).
+ Experience in technical management of package vendors and assembly houses.
**A strong advantage would be**
+ Knowledge in electrical modelisation (parasitic extraction under Cadence Xtract IM, Spice, Ansys).
+ knowledge in thermal simulations (Ansys workbench, Solid works).
+ An experience in system and sub-system development.
**A good level of English** (B2 minimum) **and French both oral and written** . Spanish would be a plus.
**What We Offer**
At Teledyne e2v, you join a team where innovation, human values and work‑life balance come together:
Work on **cutting‑edge technological projects** with high impact
Join an **innovation‑driven environment** in the Grenoble ecosystem, awarded **2026 European Capital of Innovation**
Evolve within a **human‑scale site** where your contribution truly matters
Build your career through **multiple development paths** : technical expertise, project management, and international exposure within the Teledyne group (15,000 employees worldwide)
Enjoy a **structured onboarding program** with a dedicated mentor
Work in an **attractive and flexible environment** : teleworking agreement and real work-life balance
Join a company deeply committed to **QHSE/CSR goals )** : "40 by 40" carbon plan, Gold‑level Pro Vélo certification, support to Handisport and Adapted Sport leagues
Be part of a culture built on **respect, integrity, responsibility and citizenship**
Evolve in a company committed to **gender equality** (score: 93/100)
Live in a **unique Alpine environment** , combining technological excellence with excellent quality of life
**For more information about** Teledyne Technologies - Everywhereyoulook ( **Teledyne e2v Semiconductors SAS, visit:** and all of our employees are committed to conducting business with the highest ethical standards. We require all employees to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is as important to us as our reputation for making innovative sensing solutions.
.
You may not realize it, but Teledyne enables many of the products and services you use every day **.**
Teledyne provides enabling technologies to sense, transmit and analyze information for industrial growth markets, including aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research.

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Our detailed, goal-oriented team members manage the safety profile of new drugs in clinical trials, oversee case-processing activities through all phases of development and perform regulatory reporting and medical monitoring tasks.
We hire the best, develop ourselves and each other, and recognise the power of being one team. We offer continued career advancement opportunities, award-winning training and benefits focused on the health and wellbeing of our employees.
A Day in the Life:
Responsible for the planning, coordination and delivery of signal detection and product safety scientist activities, with a focus on tasks which are low to high in complexity or which concern low to high complexity products. Additionally supports mentoring of more junior colleagues, development of processes/tools/systems, and may serve as lead on smaller FSP-type projects.
Essential Functions:
+ Serves as a creator/contributor for signal detection and product safety scientist tasks which are low to high in complexity, or which concern low to high complexity products.
+ Serves as a creator/contributor for signal detection and product safety scientist tasks which are ultra-high in complexity, or which concern ultra-high complexity products, under supervision by a more experienced team member.
+ Conducts quality review for signal detection and product safety scientist tasks which are low to high in complexity, or which concern low to high complexity products.
+ Advises clients on safety related issues under supervision by a more experienced team member.
+ Leads small FSP projects.
+ Supports training and mentoring of junior colleagues.
+ Contributes to development of processes, tools and systems.
+ Participates in bid defence and proposal development activities.
+ Works within multiple company and client systems. Interacts with project team members and clients.
+ Ensures that tasks are conducted in accordance with company policies and procedures, contractual agreements, and applicable regulations.
+ Participates in departmental initiatives; Serves as a subject matter expert in designated area.
+ Responsible for routine project implementation and coordination for assigned projects, including leading kick-off meetings, coordination of communications and data requests, participation in client meetings, audits and inspections, and review of metrics and budgets.
+ Works on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors.
+ Having wide-ranging experience, uses professional concepts and company objectives to resolve complex issues in creative and effective ways.
+ Determines methods and procedures on new assignments and may coordinate activities of other personnel (i.e., Team Lead). Exercises' judgment in selecting methods, techniques and evaluation criteria for obtaining results.
+ Frequent contacts with internal personnel and outside customer representatives.
Keys to Success:
Education and Experience:
Bachelor's degree
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
**Knowledge, Skills and Abilities:**
+ Expertise in pharmacovigilance requirements relating to marketed products and clinical trials across all major markets
+ Excellent attention to detail, data interpretation and medical-scientific writing skills
+ Advanced critical thinking and problem-solving skills with ability to evaluate and escalate appropriately Solid project management skills with the ability to manage multiple projects simultaneously and ability to redress issues proactively with limited management intervention
+ Ability to motivate, mentor and provide guidance to less experienced staff, routinely exhibiting robust and proactive scientific expertise
+ Proficient at complex project administration including budget activities and forecasting
+ Excellent oral and written English language communication skills, including paraphrasing skills
+ Advanced computer skills with the ability to work within multiple systems; advanced skills in Microsoft Office products (including Outlook, Word, and Excel)
+ Ability to maintain a positive and professional demeanor in challenging circumstances and to proactively plan for likely scenarios using personal experience
+ Ability to work effectively within a team to attain a shared goal
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Apply today! Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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.
**The role**
The Purpose of the Role is to support the development of a sustainable Lean culture by driving the elimination of waste and enabling flow of value to the customer.
The CI Engineer will demonstrate responsibility for the deployment of Lean Thinking across the site, ensuring alignment with the CI Strategy and Global Operational Excellence.
This role is 100% on site.
**Main responsibilities**
+ Create in conjunction with the CI Manager the lean vision for the site and implement the Lean Maturity Index to establish an Operational Centre of excellence.
+ Lead, Facilitate and Coach A3 projects, cross functional kaizen events and multi practitioner teams to drive best practice in process improvement.
+ Support the Sites CI by engaging with the Global Operational Excellence Lead, ensuring Global Standards are deployed (Lean Maturity Index), Site Best Practice shared, and results communicated.
+ Play a leading role within the Site Cost Reduction/Improvement Program.
+ Maintain and report Site cost saving data in support of the Business Cost Reduction Targets.
+ Lead, mentor, and Train the Site Team to raise Lean Awareness, develop the lean approach and build in lean capability.
+ Be an advocate of CI tools and strategy. Ensure the effective use of appropriate CI Methodology to challenge current thinking, deploy improvement, lock in and sustain results.
+ Use technical expertise and influence to identify opportunities for process improvement projects, aligned to the site strategy (safety, quality, delivery, cost, and people). Ensuring completion through generation of data/technical justification, implementation, and qualification.
+ Identify and utilise Electronic Data Collection Platforms and analysis tools to enable Site Performance management and control.
**Work Experience and Skills Required**
+ Able to demonstrate application of continuous improvement tools and techniques (Kaizen, TPM, SMED, RCA) to deliver positive outcomes.
+ Dynamic and ambitious professional with proven delivery record
+ Strong team player able to demonstrate ability to lead and facilitate informal and formal teams in the development and delivery of improvement solutions
+ Able to work across the Operational organisational environment
+ Must be able to work under pressure and co-ordinate multiple activities concurrently
+ Hands on approach problem solving and mind set, organised and methodical
+ Demonstrated ability to extract critical information to enable effective and appropriate decision making
+ Strong understanding of Stakeholder management tools in order to ensure engagement in change at all levels.
+ Willing to learn, develop skills and knowledge
+ People Management
+ Experience of managing finances and tracking of cost savings
**BENEFITS**
At PCI, we believe our employees are our most valuable asset. That's why we are committed to offering a benefits package designed to support your well-being and enhance your overall quality of life.
Here's what we offer:
+ Competitive salary
+ Health insurance + reimbursement for medication
+ English classes
+ Discounts on various activities
+ Partnerships with gyms
+ Referral programme
\#LI-AT1
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future ( 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._
Why work for PCI Pharma Services?
At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.
PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled