The process vision engineer will be a skilled professional that will work within the vision team, along with the other vision experts. In this position, he or she will be responsible to maintain and improve the automated visual inspection program as well as the robustness of other vision systems.
As a technical expert, he (or she) will also have to build and to manage technological knowledge for Automated Visual Inspection linked to manufacturing processes into the Production unit for syringes and/or vials. He (or she) will:
Assure proper functioning of Automatic Visual Inspection Machines in the Production unit.
Fine tune / develop new or existing vision programs to decrease false rejects or to improve detection capabilities.
Interact with production, Quality and global vision experts.
Lead and/or participate to technical investigations in case of atypical false rejects rate with the vision team, production supervision, Quality and maintenance team.
Provide vision expertise to support maintenance activities.
Develop technical knowledge in AVI with the support of local and global experts and supplier and supports field technicians as well as production performance.
Participate to the continuous improvement process performance (simplifies processes, design a short and mid-term strategy for the programable contents, lowers the false ejection rates)
Lead investigations and trials related to process improvement for vision (on the AVI machines and on the upstream process). Propose (and integrate) solutions for improvement.
Respects current Good Manufacturing Practices (CGMP) as well as GMP procedures.
Provides technical support to the deviation handling process (root causes identification and of CAPAs task execution in order to avoid recurrence of deviation with technical root causes).
Skills and Knowledge Requirements
Education : Industrial engineer (or similar level of education)
Knowledge : Automatic visual inspection, Vision systems (not necessarily linked to pharma), automated system programming.
Language : English and French.
Experience : 3-5 years' experiencein a similar function
Able to work in team in a production environment
Our offer Jefferson Wells offers you a permanent contract as a consultant with an attractive salary package and access to training in both technical and non-technical skills. We'll be your career partner every step of the way.
Execution of project management activities, including
Contract management for external parties
Managing project scope
Managing project planning (resources and material)
Controlling time management and monitoring progress
Drafting and controlling project budget
Analyzing and managing project risks
Governance & Reporting
Putting in place an effective governance
Managing reports and other necessary documentation
Ensuring internal and external stakeholders’ satisfaction
Leading project’s meetings
Coaching, mentoring and knowledge management
Organizing and motivating a project team
Developing project management best practices
Managing integration of the team’s work to the strategic objectives of the company
Drafting and sharing lessons learned
Who are you ?
A Master’s degree in business, engineering or life sciences is highly preferred.
5 years of experience in a Project Management role, or related function, within Pharmaceutical Industry or its providers. Previous experience in R&D projects is a plus.
Experience of working with global, multi-cultural, diverse, cross-functional project teams, with demanding timelines and complex deliverables
Project Management Certification or Qualification is an asset (PMP, Prince 2, Agile …).
Fluent in English. Fluency in French is a big plus.
Thorough familiarity with word processing, spreadsheet, and project scheduling computer applications.
Ability to manage multiple priorities under pressure, trouble-shoot, and to meet short- and long-term deadlines.
having a customer-centric approach when managing client projects
Agility to transition on an easy way between internal R&D and client/customers R&D projects.
Demonstrated experience in budget and financial management.
Excellent written and verbal communication skills.
Excellent critical and creative thinking.
Ability to build a trusting and safe environment where problems can be raised without fear of blame, retribution, or being judged, with an emphasis on conflicts and problem-solving.
Providing all support to the team using a servant leadership style whenever possible and leading by example
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.
Our partner is looking for an Product Managerto join its teams.
Your responsibilities?
As a Product Manager, you will have the responsibility of several product lines for biomanufacturing, with a focus on their software platform and Industry 4.0 vision. You will have the mission to define, advance and promote innovative products and software bringing significant benefits to our target markets, in line with the company’s strategic objectives.
RESPONSIBILITIES
Generate and execute the product strategy:
Develop a holistic strategy vision and roadmap combining automation, business information, and manufacturing execution architecture to drive our product portfolio towards Industry 4.0
Create and maintain a comprehensive software offering across the equipment portfolio
Work with commercial, technical and strategy leaders to develop and maintain a centralized product vision and strategy for planning and execution of new products, translating into product roadmaps, requirements, and specifications
Conduct and communicate market research and competitive analysis to drive decision-making. Develop critically justified business cases for new product development.
Articulate and document product value proposition with heavy emphasis on quantitative rationale
Define, monitor and adapt pricing strategy and profitability
Work with marketing and sales to define product positioning and commercialization strategy
Active portfolio management:
Define and implement the life cycle roadmap of current products, in line with corporate objectives and with the current and future portfolio
Monitor technical and commercial performance of the products, continuously identifying and prioritizing improvement opportunities
Define annual product/portfolio priorities and objectives in line with corporate objectives, to be deployed in sales and marketing plans and campaigns
Support creation of tools to navigate the existing portfolio
Be the Life Sciences market expert:
Communicate internally and externally to educate on and promote your product lines, e.g. application notes, webinars, conference presentations
Maintain current knowledge of market trends, competitive landscape, and events of note.
Let's talk about you !
Master and/or Engineering degree. Most preferred degrees are Automation, Bioengineer, Biotechnology, Bioprocessing or any alternative Master / Engineering degree with relevant experience
2+ years of experience as a Product Manager
4+ years of experience in manufacturing industry, ideally in life sciences (pharma, biopharma, food & beverage bioprocessing, medical device) or other regulated industry
Comprehensive understanding and experience in digital technologies, e.g. Internet of Things (IoT), AI, Edge and Cloud computing
Experience or knowledge with Industry 4.0, Digitalization, and software platforms, preferably applied to bioprocessing for biopharma
Strong understanding of portfolio management concepts including life cycle strategy, new product definition, and portfolio rationalization analysis
Knowledge of biological processes, biopharmaceuticals technologies, GMP for biological products would be appreciated
Excellent level of written and spoken English, French is a plus
Our offer?
We offer a long-term contract, a competitive salary package including company car and bonus, an wide array of extra legal advantages and the possibility of evolution in an international, dynamic and fast-growing company.
You’re interested in this job? We kindly invite you to apply.
As a member of the Automation Engineering Team in the R&D Department, you will be involved in various lifecycle phases of control systems and industrial IT.
Your responsibilities
You will contribute to the analysis of automation projects and the definition of hardware and software specifications.
You will be in charge of developing software by analyzing, programming, testing and putting into service control systems while ensuring that project documentation is in line with the procedures
You will be the owner of a ‘control unit’ and its related software solutions.
You will ensure the development follow-up, prepare work package and be responsible for the whole quality.
You will provide high-level technical support.
Your profile
Degree in Automation Engineering or in Industrial IT.
5 years of experience in operation, support and development.
PLC programming skills (we work on Siemens STEP7 and TIA Portal, B&R).
Communication skills in English and French.
Open to travel internationally for short missions (3 weekends & 2 weeks per year).
Having a driving license (B type)
SCADA programming in Wonderware Archestra, Wonderware InTouch, B&R Visual Component is an asset;
Knowledge of motor drivers and motion systems (SEW, Schneider Electric, B&R);
Analytical and critical mind, expert in providing efficient solutions to technical problems while respecting guidelines and project schedule.
Industrial IT programming (.Net, Python, SQL, Web) is an asset;
Experienced in working on projects
Our offer
Attractive salary package that corresponds to your experience level (with a company car)
Flexible home office policy
Many possibilities of evolution
A team that listens and leaves room for everyone’s development
Environment with cutting-edge technologies and challenging problems
Good work/life balance
Are you interested in this position? Don't hesitate to apply!
Notre client est une société industrielle basée dans le Brabant Wallon qui conçoit et développe des pièces mécaniques principalement pour le secteur automobile. Pour soutenir la croissance de leurs activités, nous recherchons activement un(e) Concepteur Mécanique CATIA V5.
Vos responsabilités
Vous participez à la conception au moyen d’outils CAO d’éléments et pièces mécaniques
Vous réalisez les plans des pièces, ainsi que les plans d’assemblage sur base du dossier de pré-étude et des contraintes de fabrication.
Vous développez et gérez les dossiers d’industrialisation.
Votre profil
Bachelier en mécanique ou électromécanique
Expérience de minimum deux ans en conception mécanique
Vous présentez un bon niveau en anglais (minimum B1)
Vous maîtrisez le logiciel Catia V5, V6 et/ou NX Unigraphics
Une expérience de l’injection plastique ou la maîtrise de Moldflow serait un plus
Rigueur, méthode et sens des responsabilités vous caractérisent
Notre offre
Jefferson Wells vous propose un contrat permanent en tant que consultant avec un package salarial attractif et vous donnera accès à des formations dans les domaines techniques et des compétences non techniques. Nous serons votre partenaire de carrière à chaque étape de votre parcours.
Ce poste vous intéresse ? N'hésitez pas à postuler !
Profil expérimenté – Minimum 3-5 ans d’expérience dans le sujet
Autonome
Capable d’agir sous la pression
Organisé
Notre offre Si vous êtes passionné(e) par l'innovation et que vous souhaitez contribuer à un projet stimulant au sein d'une entreprise de renommée mondiale, postulez dès aujourd'hui à notre offre. Jefferson Wells s’engage à vous offrir un contrat en consultance, un accompagnement rapproché ainsi qu’un salaire et un package attractifs. Des questions ? Vous souhaitez soumettre votre candidature ? Envoyez un mail à [email protected] .
Réalisation des expériences de laboratoire définies avec le responsable de projet
Manipulations en laboratoire afin de reproduire à petite échelle les étapes secondaire de production de nos vaccins : Media Preparation – Formulation – Filtration – Filling –Lyophilization en utilisant les techniques tel que : pH, Conductivité, Osmolarité, Viscosité, Turbiscan (vitesse de sedimentation), Néphélométrie, SLS et/ou DSL, Occhio, FTU units
Interprétation de la signification de ses résultats de manière assistée et conclusion scientifique
Rédaction d’un cahier de laboratoire de manière autonome et en respectant les procédures en place
Gestion du planning de vos manipulations
Parlons de vous !
Vous êtes en possession d’un Bachelier à orientation scientifique (Chimie, Biochimie, Biologie, …) ou d’un A2 (CESS) avec une expérience probante
Vous avez idéalement une première expérience en laboratoire dans un environnement pharmaceutique ou associé et vous avez les bases pour pouvoir manipuler sous flux laminare
Rigoureux(se), précis(e) dans vos tâches, vous avez l’esprit analytique et un bon sens critique
Vous savez travailler en équipe, êtes ouvert(e) au changement et à l’innovation.
Ce que nous pouvons vous offrir ?
Jefferson Wells te propose un contrat permanent en tant que consultant avec un package salarial attractif et te donne accès à des formations techniques et en compétences interpersonnelles. Nous serons ton partenaire de carrière à chaque étape du parcours.
Our partner is looking for a Analytical Methods Validation Physico to strengthen its team. This international company is well-known for its research, development, and marketing of pharmaceutical and vaccines.
What are your responsibilities?
Scientist for Andrew+ automation strategic intent both vaccines and pharma
Andrew+ POV
Client/Server solution
Validation guidelines
To plan and work with several department to deliver a proof of value and provide guidelines for automate and automation software validation
To build and track global timelines.
Organize and participate to core team and Steerco meetings.
To track and maintain project deliverables, timelines, and budget
To formulate the overall project success and calculate savings/gains.
Key Deliverables:
MSP Online project plan
Decks for core team and steering comities
Global savings/gains documents
URS and IQOQPQ validation documents
Analytical method Qualification/Validation protocol and reports
Statistical analysis
Who are you ?
Master’s degree, Sciences or equivalent acquired through experience
Experience in GMP QC testing
Computer skills in excel, word, outlook, PowerPoint and MS Project
Experience in statistics
Experience in Computer system validation methodology
Competences:
Knowledge of laboratory operations.
Tech background
Strong analytical skills to address challenges.
Excellent written and oral communication skills in English. Build trust.
Ability to work under pressure due to the requested flexibility and reactivity of the activities
Ability to work in project teams in a multidisciplinary environment.
Understanding of the requirements of GMP environment and Data Integrity and Computer System Validation.
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.
Brabant Wallon – contracting Life cycle & Change Control Specialist
What are your responsibilities?
Develop further the process to prepare content on change controls for communication to external partners.
Manage meetings with external stakeholders and present information to Quality, regulatory and technical collaborators
Organize the transfer of information on change controls between GSK and QA department from external partner
Collaborate with people located in MPU’s and abroad. Convince them vis-à-vis decisions, procedures or processes, while remaining diplomatic and maintaining motivation.
Be able to manage internally (between colleagues from different departments) as well as externally.
Efficient follow-up to respond to any questions and respect the timings of the projects.
Establish & track key performance indicators for each step of the process
Lead the design of or optimization of process
Follow the implementation of changes and ensure alignment with RA and external partners to minimize the impact on supply continuity.
Write local SOP with new process, and ensure training of all stakeholders (MPU, QA, QC, site conformance, RA, MSAT).
Be responsible for the change controls specific to GSK working for an external partner
Collaborate on punctual projects such as participation to taskforces, development of standards
Who are you ?
Experience (preferable 5 years) in the following would be considered an asset :
(Bio)pharma & cGMP
Quality
Project management
Technical lifecycle
Bilingual French/English (oral & written)
Proactive with ability to identify and follow up on gaps in process
Ability to work under pressure due to the requested flexibility and reactivity of the activities
Be able to manage short term issues with long term activities in parallel.
Ability to work in project teams in a multidisciplinary environment and a matrixial organization
Be able to lead and manage cross-functional projects
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.
R&D clinical Contracting – Braine l’Alleud Our client is looking for a profile to fill a position in R&D clinical development. The role involves clinical studies in F1 and F2.
What are the responsibilities? • Activities related to the design, and everything related to the analytical development. • Taking the lead on protocols studies
Experience and Knowledge requirement • Proven project management skills • Experience in medical monitor for vaccines studies • Degree or background in the medical field or proven experience • Nice to have: clinical method development plan management • Fully fluent in English both written and spoken
Our offer? Jefferson Wells offers you a permanent contract as a consultant with an attractive salary package and access to training in both technical and non-technical skills. We'll be your career partner every step of the way. Are you interested in this position? We invite you to apply. Do you have any questions? Please contact Aylin Ugurlu at [email protected]
