Evaluation Engineer – Automotive

  • Location: Brussels
  • Type: Contracting
  • Job #20245

Brussels – Contracting

#productevaluation #automotive #engineering #english

For our client, specialized in automotive interior parts, we are looking for an Evaluation Engineer – Automotive.

The Evaluation Engineering Department is responsible for coordination and execution of the company product evaluations for automotive seats of Europe and Africa region projects, cost reduction activities and serial production projects.

Responsibility of the function starts with required evaluation selection according to development targets/product characteristics in close communication with colleagues from the R&D department within the company and continues with planning and execution until all evaluations are finalized and result outcome is examined. You will analyze the failure reason and support design departments in countermeasure development by providing technical insight.

What are your responsibilities?

  • Select and schedule necessary evaluations for projects, serial production and cost reduction activities.
  • Prepare correct test setup according to technical standards and receive reliable evaluation results.
  • Understand and examine evaluation results, report and communicate results to related parties.
  • Support plants/serial production on problem analysis and support in developing countermeasures for serial production issues.
  • Prepare reports for project milestone meetings.
  • Work and communicate closely with related parties in following up ongoing and planned evaluations and problem analysis.
  • Continuously focus on improving quality of evaluation output by studying and comparing test method to known standards and implement improvement actions.

Who are you?

  • Bachelor or master degree in engineering field, preferably in mechanical or industrial engineering or equal.
  • Experience in product evaluation and product design is considered an asset.
  • You have a hands on mentality and are able to work independently.
  • Team player.
  • Strong communication skill.
  • Advanced knowledge of MS Office.
  • Basic knowledge of CATIA is an asset.
  • Working level efficiency in English.
  • Willing to travel abroad for short to mid long terms (5-15%)
  • No physical restriction to handle/lift/carry parts (max 25 kg)

What can you expect ?

Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way.

Are you interested in this job? Don’t hesitate to apply !

Material Engineer – Automotive

  • Location: Brussels
  • Type: Contracting
  • Job #19982

Brussels – Contracting

#automotive #materialengineer #chemicalengineer #REACH #IMDS #datamanagement #plasticparts #chemical

For our client, leader in the automotive sector, we are looking for a Material Engineer – Automotive.

What are your responsibilities?

  • Activities :
    • Managing chemical substances: REACH and IMDS
    • Plastic material evaluation
    • Suppliers management
    • IMDS data management from suppliers (+- 3000 parts)
      Following up and correct mistakes
      Checking with internal system
    • Recycling of plastic parts, new materials validation, lab tests
      Checking and confirming results in regard to the company requirements and make hypothesis.

​​Who are you?

  • Master’s degree in Material Engineering or Chemical Engineering
  • Junior or internship/first experience in a chemical company, chemical knowledge
  • SW : office package + knowledge of excel
  • Good communication skills
  • Fluency in English
  • Plus: you will be trained in IMDS/REACH

What can you expect?

Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way.

Are you interested in this job? Don’t hesitate to apply !

Technicien de laboratoire

  • Location: NEDER-OVER-HEEMBEEK
  • Type: Contracting
  • Job #20192

Technicien de laboratoire

Bruxelles – CDI

#Techniciendelaboratoire #chimie

Notre client de l’industrie chimique est à la recherche d’un Technicien de Laboratoire pour apporter un support au département R&I.

Quelles sont vos responsabilités?

Les missions suivantes vous seront confiées dans un premier temps:

  • La formulation avec des solvants de matériaux organiques, la dispersion et le mélange de matériaux inorganiques au laboratoire et le traitement à (petite) échelle pilote.
  • Le revêtement de films minces par coulée ou revêtement par fente dans le laboratoire chimique ou dans le laboratoire en chambre sèche
  • Traitement par extrusion dans un petit pilote.  
  • Incorporation dans des batteries (piles à pièces) des matériaux préparés, caractérisation des batteries en collaboration avec des scientifiques experts.
  • Opérations en boîte à gants
  • L’analyse des données et la préparation des rapports

Quel est votre profil?

  • Vous pouvez démontrer une expérience pertinente en laboratoire de chimie et avec des équipements de traitement à l'échelle pilote.
  • Vous disposez d’un bachelier en chimie, physique, sciences de la vie.
  • Vous avez un bon niveau en Excel et Google apps, bonne connaissance de la plateforme office (word, power point) 
  • La connaissance de l'ELN (electronic lab-book) est appréciée.
  • Vous parlez Français et avez un bon niveau d'anglais (parlé, écrit)
  • Attitude positive vis-à-vis de la collaboration, du travail en équipe et de la sécurité.

Ce que nous vous offrons?

Un CDI avec un package salariale correspondant à votre expérience et compétences. L'opportunité de développer vos compétences au sein d'un grand groupe Chimique de renommée international.

Ce poste vous intéresse? Si vous avez des questions n'hésitez pas à contacter Sophie Rolis [email protected]

Production Engineer Junior

  • Location: Brussels
  • Type: Contracting
  • Job #20132

Brussels – Contracting (CDI)

#production #engineering #industrial #junior

Our partner is a manufacturer of high qualitative products used for decoration of signalization on cars, machines and buildings. 

They are looking for a Production Engineer Junior to manage operational
projects while monitoring, summarizing, communicating, and reporting status to the
Operations Manager.

What are you responsibilities ?

  • Participating in operational meetings and QC workshops
  • Observing and learning from experienced staff members
  • Taking the lead of small operational teams​​
    • Organize the capacity according to forecast
    • Defining priorities of production orders in line with the production
      planning
    • Measuring and follow up of the production performance
    • Taking initiatives to align the productivity to the objectives defined by
      Operations Management​​
  • Analyzing the production efficiency based on data registered by the planning
    tool
  • Optimizing cost calculation methods
  • Take responsibility of operational improvement project(s) assigned by the Operations Manager, such as Lean Manufacturing, etc.

Who are you ?

  • Civil engineer mechanics or Industrial engineer
  • A first professional experience in production is an asset
  • You can speak French and English. Dutch is a plus
  • Hands on mentality

What can you expect ?

Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way.

Are you interested in this job? Don’t hesitate to apply !

Maintenance Manager

  • Location: Brussels
  • Type: Contracting
  • Job #20128

Brussels – Contracting (CDI)

#maintenance #production #facilitymanagement 

Our client is a manufacturer of high qualitative products used for decoration of signalization on cars, machines and buildings. The machine park is state-of-the-art and continuously innovated in line with the strategy to achieve high standards for customers. 

There is a very large variety of production methods and as such, lots of different machines. 

We’re looking for a Maintenance Manager who can take responsibility of the technical and mechanical part of our production processes, in close collaboration with the Operations Director. 

What are your responsibilities ? 

  • You are responsible for the management of the machine park.  You organize the preventive maintenance, and you coordinate the curative maintenance
  • You support the operators in the executing of maintenance tasks that can/must be done 
  • You try continuously to search for optimizations in the production processes from a mechanical and technical point of view
  • You investigate the possibilities to automate production steps
  • You follow the trends in the fast changing technologies used in the graphical industry
  • You manage the contacts with the machine suppliers
  • You define the IT-system that supports the management of all data linked to the maintenance and the suppliers of the machine park.
  • You assure that the operations can be performed in a secure modus
  • You take full responsibility of the facility management of the new building

Who are you ?

  • Civil engineer mechanics or Industrial engineer
  • You can speak French and English. Dutch is a plus
  • Able to work independently, but also in collaboration with Operators, Team Coaches, Production managers and the Operations Director.
  • Strong analytical skills, especially linked to the technical aspects of machines.
  • Able to communicate with suppliers all over Europe.
  • Hands on mentality

What can you expect ?

Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way.

Are you interested in this job? Don’t hesitate to apply !

Battery Modelling Engineer – Automotive

  • Location: Brussels
  • Type: Contracting
  • Job #20073

Brussels – Contracting

#modelbaseddesign #automotive #battery #batterymodelling #dataanalysis #datascience #matlab #simulink #python

Our client is a leader in the automotive sector.

You will join the digital MBD (Model Based Design) team which is part of the Powertrain Engineering group. The target of Battery MBD is to identifiy the EU new technology and to integrate it into the model in order to propose battery system design & evaluate battery performances with MBD. In parallel to challenge new modeling methodology with machine learning to make model efficiently & improve the model accuracy.

What are your responsibilities?

You will be working within battery team, tasks will include:

  • Technology research : research the latest battery MBD technology & battery related connected service to develop new MBD method/ improve existing method following conference etc…
  • Methodology development:
  1. Develop the MBD methodology to reduce battery cell evaluation.
  2. Challenge to reduce testing & required cells based on existing test data.
  3. Replace actual evaluation to simulation for further improvement.
  • Model validation : Validate existing model in EU customer condition.
  • Data analyzing: analyses simulation & test data and draw conclusions.
  • Field issue research : Research BEV/Battery related field issue in EU.
  • Team support: take a role of expert in the field, contribute to the team overall outcome, support problem solving.

Who are you?

  • Experienced in:
  1. Battery modelling & data analysis
  2. Battery pack/cell test & results analysis
  3. Machine learning /Data science knowledge ( Preferable)
  • Open, highly motivated personality with hands-on mentality, able to work in an independent way as well as cooperate and deliver to the team
  • Able to summarize and explain complex technical information in a clear and visual way.
  • Required computer skills: MS Office, MATLAB, Simulink, Python
  • Must be able to effectively & clearly communicate in English (written & spoken)

What can you expect ?

Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way.

Are you interested in this job? Don’t hesitate to apply !

Qualification/Validation – Metrology Officer

  • Location: Drogenbos
  • Type: Contracting
  • Job #20101

Qualification & Validation – Metrology Officer

Brussels – contracting

Our partner is looking for a Metrology Officer to reinforce its team. This international company is well-known for its research, development, and marketing of pharmaceutical. 

What are your responsibilities?

  • Carries out qualification and validation activities according to the validation master plan.
  • Participates in quarterly qualification and validation review meetings
  • In consultation with the teams involved, ensures the drafting of all documentation relating to : the qualification of equipment, premises, software,… (Validation plan, protocol and report DQ, IQ, OQ and PQ as well as the final report,…).
  • Process validation (manufacturing, packaging, cleaning, automation…) (Validation plan, protocol and report,…).
  • To the metrology of the site (specifications, deviation report,…)
  • Ensures that the tests and specifications proposed in the protocols are developed in agreement with the managers/directors of the departments involved and the quality director.  
  • Ensures that people are trained in qualification activities. 
  • Prepare, supervise and coordinate the qualification and validation tests with the operational teams. (production, supply, lab…)
  • Ensures the collection and control of qualification and validation results, alerts and manages discrepancies in agreement with the managers, directors of the departments concerned and the quality director.
  • Writes and updates procedures related to manufacturing, packaging, cleaning, qualification and validation processes…
  • Participates in risk analyses concerning processes (manufacturing, packaging, etc.)
  • Supervises, coordinates and ensures the metrology activities in accordance with the specifications, the validation master plan and associated procedures.
  • Controls metrology reports, alerts and manages deviations in agreement with the managers, director of the concerned departments and the quality director.
  • Participates in qualification activities, validation of new projects of the site
  • Resolve CAPAs related to the qualification, validation & metrology department
  • Ensures the drafting of all documentation related to the qualification, validation and metrology services according to the needs.

Who are you?

  • You have a Master of Science or Bachelor of Science degree with solid experience in qualification/validation
  • You have experience in the pharmaceutical industry 
  • You are accurate and rigorous
  • You have an analytical mind
  • You are Team player
  • You have a good interpersonal skills, with good communication skills

What can you expect?

Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way.

You’re interested in this job? We kindly invite you to apply. Do you have any questions? You can contact Marie Rossenfosse: [email protected]

Technicien de laboratoire QC

  • Location: Bruxelles
  • Type: Contracting
  • Job #16545

Technicien QC

Bruxelles – CDI

#GMP #QC #quality #control #analytical #laboratory

Vous êtes orienté contrôle qualité et laboratoire ? La rigueur est votre maître-mot ? Alors ce qui va suivre va vous intéresser !

Notre partenaire est activement à la recherche d’un technicien QC pour rejoindre son équipe. Il s'agit d'une société active dans le secteur pharmaceutique située à Bruxelles.

Quelles sont vos responsabilités ?

  • Vous analysez et interprétez ces analyses pour les matières premières, IPC, intermédiaires, produits finis et échantillons de stabilité
  • Vous garantissez le double-check des analyses de vos collègues et vous réalisez des maintenances d’appareil si nécessaire
  • Vous réalisez des études d’applicabilité par Karl-Fisher
  • Vous dirigez ou participez à des projets d’amélioration continue du laboratoire QC

Qui êtes-vous ?

  • Vous possédez un bachelier en chimie ou biochimie
  • Vous maitrisez les techniques analytiques physico-chimiques telles que HPLC, GC, UHPLC, titration, UV, ….
  • Vous avez une expérience dans un environnement (c)GMP
  • Une première expérience dans une fonction similaire est un grand atout
  • Vous êtes ouvert à travailler en 2 pauses (6h-14h/ 14h-22h)

Que pouvez-vous espérer ?

Notre client vous offre un package salarial attractif complété d’avantages extra-légaux et l’opportunité d’évoluer au sein d’un groupe dynamique et innovant.

Si vous êtes intéressé, n’hésitez pas à me contacter, via [email protected]

Nous n’attendons plus que votre candidature pour discuter de votre projet professionnel.

Electric Motor – Voltage Engineer

  • Location: Brussels
  • Type: Contracting
  • Job #19764

Brussels – Contracting

#electricmotor #voltage #automotive #engineering #JMAG #matlab #ansysmaxwell  

For our client, leader in the automotive sector, we are looking for an Electric Motor – Voltage Engineer.

What are your responsibilities?

  • Working with technician team to setup e-motor bench.
  • Prepare test instruction to measure surge voltage.
  • Run experiment & support technician team during test campaign.
  • Record & analyse test results to ensure correct test procedure.
  • Indicate surge voltage in different conditions based on test results.
  • Run & modify existing models to calculate surge voltage.
  • Use JMAG or Ansys Maxwell to calculate electromagnetic behaviour of e-motor.
  • Use MATLAB to simulate electronic circuit of e-motor & calculate surge voltage.
  • Compare surge voltage calculated by model versus measured at bench & verify simulation method.
  • Regular report & presentation to update the project progress in meetings.
  • Collaborate with technician/evaluation/design/MBD team.
  • Cooperate with current team to perform smooth hand over.
  • Research & survey to find measurement & simulation method of surge voltage in vehicle.
  • Contact EU resources who can measure/model surge voltage in vehicle & arrange meeting/discussion to understand their competencies.
  • Prepare proposal for future projects: vehicle measurement/model, improvement…
  • Writing report & prepare slides.

Who are you?

  • Electro-Mechanical Engineer.
  • Experience in (based on priority):
  1. Electric motor design & optimisation
  2. Electric motor/ vehicle impedance analysis
  3. Electromagnetic modelling & electric motor analysis
  4. Electric motor test & results analysis

What can you expect?

Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way.

Are you interested in this job? Don’t hesitate to apply !

Clinical Research Leader

  • Location: Brussels
  • Type: Contracting
  • Job #17833

Will you be our new ambassador?

Jefferson Wells Life Sciences specializes in supporting pharma & biotech companies in their daily challenges. Hence our interest in experts like you to join our team. 

Let's look together at your first challenge with us!

Clinical Research Leader

This Clinical Research Leader will be responsible for leading and supporting one or several clinical trials within the Clinical R&D Department while fostering strong, productive relationships with colleagues across the organization.

DUTIES & RESPONSIBILITIES
Under minimal supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate procedures and guidelines, this position:
• Serves as a Clinical Research Leader within the Clinical R&D Department to execute and manage company sponsored clinical trials, ensuring compliance with timelines and study milestones, for Operating Company;
• Oversees/executes feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures;
• May serve as the primary contact for clinical trial sites (e.g. site management);
• Develops clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports);
• Ensures applicable trial registration (e.g. on www.clinicaltrials.gov) from study initiation through posting of results and support publications as needed;
• Manages/oversees ordering, tracking, and accountability of investigational devices and trial materials;
• Interfaces and collaborates with site personnel, IRBs/ECs, contractors/vendors, and company personnel;
• Interfaces, collaborates and oversees Clinical Research Associates (CRAs);
• Oversees and supports the development and execution of Investigator agreements and trial payments;
• Is responsible for clinical data review to prepare data for statistical analyses and publications;
• May perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close out visits based on study need;
• May contribute to the development and delivery of appropriate global evidence generation strategies (EGS) and evidence dissemination strategies (EDS), with collaborative relationships with all relevant Clinical R&D partners and cross-functional partners (e.g. Global Strategic Marketing, Medical Affairs, Regulatory Affairs, Health Economics and Market Access, R&D, etc), contributing to cross-functional alignment;
• May provide on-site procedural protocol compliance and data collection support to the clinical trial sites;
• Contributes to the critical assessment of the literature and to the interpretations and disseminations of all evidence generated;
• Is responsible for delivery of assigned clinical projects, through effective partnership with the study core team leading to delivery of clinical project commitments (deliver on time, within budget and in compliance with regulations and SOPs);
• Supports planning, track and manage assigned project budgets to ensure adherence to business plans;
• Supports clinical scientific discussions with regulatory agencies/ notified bodies to drive support of the clinical and regulatory strategy;
• May serve as the clinical representative on a New Product Development team;
• May assist with the development of Post-Market Clinical Follow-up (PMCF) Plans and PMCF Evaluation Reports (ER) within the defined timelines and review/update at planned intervals; May assist with maintaining the overview to assure (study) commitments are timely and properly met by coordination of specific documentation and contribution to cross-functional review of associated documents where relevant;
• May conduct review of promotional materials to ensure fair-balance, accuracy in clinical claims
and messaging;
• Manages and/or mentors resources assigned to designated clinical studies to provide quality deliverables while maintaining optimal efficiency;
• May act as Clinical Safety Coordinator (See ANNEX I – Clinical Safety Coordinator Duties and Responsibilities);
• May perform other duties assigned as needed;
• Is responsible for communicating business related issues or opportunities to next management level. Function as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders;
• Is responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures;
• Should develop a strong understanding of the pipeline, product portfolio and business needs;
• Generally manages work with limited supervision, dependent on project complexity.
Independent decision-making for simple and more advanced situations but requires minimal guidance for complex situations.

EXPERIENCE AND EDUCATION
Education
• Minimum of a Bachelor’s Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required.

Experience
• BS with at least 6 years, MS with at least 5 years, PhD with at least 3 years of relevant experience preferred.
• Previous experience in clinical research or equivalent is required.
• Experience working well with cross-functional teams is required.
• Relevant industry certifications preferred (i.e., CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR, MEDDEV,…).
• Clinical/medical background is a plus.
• Medical device experience is highly preferred.

REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and
AFFILIATIONS

Functional and Technical Competencies:
• Good understanding of clinical research science and processes along with an understanding of product development processes, team dynamics, related healthcare market environment, clinical trends, and global clinical trial regulations;
• Ability to provide scientifically strategic and scientific clinical research input across New Product Development (NPD) and Life-Cycle Management (LCM) projects;
• Proven track record in delivering clinical projects within clinical/ surgical research setting, on time, within budget and in compliance to SOPs and regulations;
• Strong presentation and technical writing skills;
• Strong written and oral English communication skills;
• Demonstrate competencies in the following area are required:
• Behave and lead in a professional and ethical manner
• Advanced project management skills with ability to handle multiple projects

Leadership Competencies:
Ability to lead small study teams to deliver critical milestones, as may be assigned. Leadership required in alignment with Company Leadership Imperatives:
• Connect – Develop strong collaborative relationships with key internal and external stakeholders.
• Shape – Make recommendations for and actively participate and lead in departmental process improvement activities.
• Lead – Take ownership in critical scientific thinking and development of self and engage in transparent and constructive conversations.
• Deliver – Strive to ensure all deliverables on allocated studies and those of any direct reports are met on time, within budget and in compliance with SOPs and regulations.

 

What can Jefferson Wells do for you?

As an ambassador you have the opportunity to grow within international companies where you can build a strong network. Through a personal follow-up, you receive quality support in every step that you accommodate. Finally, you enjoy the opportunity to develop yourself personally and professionally through internal training and education.

Are you interested? Apply now by clicking on the button!