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Niveau van het gemiddelde loon tijdens de laatste 12 maanden: "Manager in "

Valuta: EUR USD Jaar: 2021 2020
Op de staafdiagram is de verandering van het gimiddelde loon van het beroep Manager in getoond.

Indeling van de "Manager" vacatures in de regionen

Valuta: EUR
Volgens het diagraam zijn er in het grootste aantal vakatures van de beroep Manager in geopend. Op de tweede plaats staat {regionPName2} en op de derde {regionPName3}.

Top van de gelijkaardige vacatures volgens niveau van het loon in

Valuta: EUR
Volgens het diagraam zijn er in het grootste aantal vakatures van de beroep Manager in geopend. Op de tweede plaats staat {regionPName2} en op de derde {regionPName3}.

Aanbevolen vacatures

Brand Manager Trainee
Bel Group, Nivelles
We are looking for a Brand Manager Trainee to join our local Marketing team in Nivelles, Belgium.  You will be offered a position in a multi-functional Brand team consisting of managers with different functional expertise and background (Brand Management – to which you will report, Sales, Finance, Product Supply, Advertising and Media agencies). You will support the marketing team of Maredsous, Mini Babybel and Kiri. • Helping on the new launch of a product. • Leading campaigns briefs with various agencies (regional campaign localization or local campaign build up) & follow up on execution • Supporting in the execution of brand campaigns (media, digital, CRM, instore).  • Co-leading the digital marketing on the brands (Facebook & YouTube) • Assuring the preparation of the sales meetings and provide a marketing support to the sales force  • Supporting Brand Managers in events organization (internal and external) • Conducting market and competition studies  Searched Profile What We Are Looking For To be considered for this position you must be able to demonstrate the following: Mandatory Bachelor student or higher in Marketing or Business or Communication  Excellent execution skills Attention to details Strong communication skills Pro-active/initiative-taking mindset Fluent in French  Preferred Fluent in Dutch and English Experience within a retail environment (in FMCG) Comfortable with consumer analytics  Previous experience in a Marketing, Trade Marketing or Sales department Responsible Of The Trainee  Ilse VEUGELERS, Group Marketing Manager We offer The internship is proposed for 3-4 months minimum / up to 6 months.  We will provide you a great opportunity to develop your skills and experience with iconic brands in a very friendly environment. The internship is being unpaid.  
Manager Quality Control
GSK, Wavre, Walloon Region, be
Job Purpose:Guarantee results delivery according to standard lead-time with compliance regarding quality and EHS requirements, and in alignment with QA partner.Be accountable for capacity risk assessments (people/equipment/change control) and will propose solutions/mitigations with other QC partners (ex: infrastructure, lab support, …) or proactively escalate blocking points.Be responsible for managing change (organization, capacity, process, mindset, within his/her team) is a key success factor (ex: implementation of digital solutions, lean-lab, automation, TroubleshootingContribute to the scientific and technical assay strategy, design and optimization in agreement with pharmacopeia, CAP and GMP requirementsSupport root cause analyzes and troubleshooting activities and innovative TechnologiesCould coordinate testing activities for the QC department in agreement to GMP requirementsYour Responsibilities:Motivate and encourage a team of Technicians to achieve maximum productivity with good management of priorities and team well-being.Provide technical support to your direct reports.Organize and monitor the performance progress efficiency of the team through performance indicators related to Safety, Quality, Supply, Cost for example.Escalate proactively risks & problems and propose solutions.Ensure compliance of the operations with GMP and Authorities requirements in collaboration with QA.Develop your team and act as a coach for them.Anticipate potential improvements, implementation of corrective and preventive actions. You will also be responsible to drive continuous improvement in the team.Fulfill the role of a subject matter expert for assays, set up and oversight assays required to release GSK Vaccines. Develop technology and scientific expertise of the platform through participation to scientific meetings and congresses. Provide scientific coaching/training to other scientists and supervisors.Provide support for the development and/or review of internal and external publications, technical documents and communications.Be the technical reference for scientific and technical activities (internal and external): – internal activities related to assay development and validation, assay maintenance and testing performed under its responsibility.Participate to the follow up of collaborations with other teams/experts to share/gain scientific and technical expertise and for technology transfer within and outside GSK VaccinesParticipate to QC knowledge management in the field of expertise.Why You?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:You hold a Scientific University Deree or equivalent scientific background.Practical and theoretical knowledge in the domain of laboratory activity (eg. Biochemistry, Virology,…)You have proven experience of leading and managing a lab team.You have at least 10 years of professional experience including at least 8 years of relevant experience preferably within R&D, GIO/Q or similar roles in Pharma industry.You have a strong knowledge of international regulatory requirements that apply to vaccines (and beyond to manufacturing) and in depth knowledge of cGMP.You are a strong collaborator with ability to influence, to work in project teams in a multidisciplinary environment and a matrix organization and to work effectively across boundariesYou have the ability to develop a strong vision, and set direction in this domain, while being inspiring, and having a positive and optimistic attitude in managing day-to-day activities.Relevant experience in change management, project management and lean management could be an advantage.You are bi-lingual French/English, written competencies in EnglishPreferred Qualifications:If you have the following characteristics, it would be a plus:Good communication skillsAutonomousHands-on mentalityContinuous Improvement Mindset
Manager, Global Regulatory Affairs
GSK, Wavre, Walloon Region, be
As a Manager, Global Regulatory Affairs will have global responsibility (for Regulatory Affairs) of given activities for a Project/Product within GSK Vaccines.The purpose of the job is to:Provide input to/manage regulatory activities in order to obtain Marketing Authorisations for commercial products as rapidly as possible, with the best possible label, and to maintain these authorisations.Determine from a strategic and scientific perspective the content of relevant sections (technical/non-clinical (NC), clinical/labelling or procedural) of project/product specific documents submitted to regulatory agencies worldwide (eg. MAA/BLA, variations/sBLA, Q&A, scientific consultations, Paediatric Investigational Plans, etc.) and ensure that these documents meet high scientific standards and regulatory requirements. Responsible for one specific (clinical/labelling or technical/NC or procedural) section.Provide support in compiling/write briefing documents for internal governing bodies and other relevant internal documents (eg Global Regulatory Plan, KMS, etc.). Responsible for one specific section (clinical/labelling or t/NC or procedural).Support the Global Regulatory Lead in providing robust regulatory advice and plans to the various project teams and advisory bodies to ensure that the business needs are in compliance with regulations and/or regulatory advice received from the agencies.This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:Provide support to the Global Regulatory Lead (GRL) for key regulatory activities pertaining to a project/product.Interact with (or represents his/her area/product at) internal project related teams (e.g. LTT, SRT etc.) and possibly project teams (PTs), for clinical/labelling or technical/CMC or procedural aspects of a given project.Participate to project/product-related discussions and provides in-depth strategic, scientific and RA input, for clinical/labelling or technical/NC or procedural aspects of given project.Provide in-depth input into the asset specific regulatory strategy on a global scale for clinical/labelling or technical/NC or procedural aspects.Coordinate (for one specific clinical/labelling or technical/NC or procedural part) the determination of key messages for product/portfolio specific regulatory documents to be submitted to Authorities, in collaboration with the GRLCompile/write high quality project/product specific regulatory documents to be submitted to Authorities (for clinical/labelling or technical/NC or procedural sections) and ensure that those documents meet regulatory requirements.Facilitate and deliver the regulatory strategy to support the lifecycle of the asset; contribute for clinical/labelling and/or technical/NC and/or procedural aspectsMay possibly act as the point of contact for Regulatory Agencies for asset(s) (project-specific)Provide support to the GRL to assure efficient interactions with the regulatory authorities to achieve on-time approvals of GSK Vaccines submissions for the asset(s)Must be aware of changes in regulatory guidelines and their impact on regulatory strategy for the particular asset(s).Develop and motivate collaborators (within RA team or for one of the RA aspects with multidisciplinary teams) to achieve quality output, accountability and recognition across the organization and towards the regulatory authorities.Ensure planning and proper organisation of activities (for one of RA specific activities within clinical/labelling or technical/NC or procedural) in line with the overall project plan and RA milestones.Why you?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:Ph.D. or M.D in Pharmacy, Chemistry,Biologyor Medicine 4+ years significant experience in regulatory affairs, or appropriate relevant experienceAbility to coordinate and execute regulatory strategy for a given project/product.Strategic thinker – ability to provide input into regulatory strategy and evaluate potential impact on overall project/product strategy.Ability to identify and escalate issues to the GRL and to propose mitigation strategies, maximise opportunities, with proven ability to develop collaborative relationships and have high impact and influenceFluent in English, with excellent writing skills.Preferred Qualifications:If you have the following characteristics, it would be a plus:Previous experience in the development of medicinal products and obtaining licenses in different geographical areas is preferred.Ability to coordinate and execute regulatory strategy for a given project/product.Strategic thinker – ability to provide input into regulatory strategy and evaluate potential impact on overall project/product strategy.Ability to identify and escalate issues to the GRL and to propose mitigation strategies, maximise opportunities, with proven ability to develop collaborative relationships and have high impact and influenceGood presentation skills to ensure that GSK Vaccines regulatory voice is clearly articulated and heard in the various cross functional teams.Support the Global Regulatory Lead to ensure regulatory input is provided to other GSK divisions or to regulatory agencies, as appropriate.Good influencing skills.Ability to collaborate with other departments and teams in the delivery of outputs in a timely mannerAbility to resolve problems through resourceful use of information and contacts.Enterprise thinking – needs to understand the constraints and drivers of other functions and the potential impact on RA, including how RA may facilitate in achieving the overall goal.Quality mindsetAble to input into the Company’s regulatory positioning, and write /critically review key documents targeting internal or external key audiences.In collaboration with the function and regions, ensure rigorous scientific content/quality/compliance of documents intended for regulatory submissions
Manager, CMC Vx Development Projects
GSK, Wavre, Walloon Region, be
Are you seeking an opportunity where you can lead through influence using your expertise? If so, this Manager, CMC Vx Development Projects role could be an exciting opportunity to explore! This role will provide YOU the opportunity to progress YOUR career, these responsibilities include some of the following…Identifies risks associated with submission data and information packages.Contributes to, and leads (as required) the creation, maintenance and continuous improvement of CMC Regulatory processes, policies and systems Contributes to, and leads (as required) the creation, maintenance and continuous improvement of CMC Regulatory processes, policies and systemsWhy you?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:Bachelor’s degree in Sciences or Medical Sciences0-3+ years of relevant industry experience in product developmentExperience managing multiple projects simultaneously.Knowledge of drug development and manufacturing and supply processes and may have a specialized area of expertise.Preferred Qualifications:If you have the following characteristics, it would be a plus:Master’s degree or above in Chemistry, pharmacy, biological or closely related science advanced degree.Regulatory Affairs Certification (e.g. RAPS).Demonstrated ability to handle global CMC issues through continuous change and improvementExperience in Pharmaceutical industry or Research organizations, established in Regulatory Affairs and with demonstrated experience of leadership in a matrix environment.Sound knowledge of vaccines/biological products development, manufacturing and supply processes.Continued professional growth in global regulatory affairs including communication of evolving/emerging trends and policies. Has identified opportunities to further educate colleagues and formulate approaches to most effectively meet new requirements.Identified as CMC Regulatory expert in a specific subject area.Highly developed interpersonal, presentation and communication skills.Proven experience in training staff within an organisation.
Project Manager Services
Alstom, Charleroi, Walloon Region, be
Req ID:96973 We create smart innovations to meet the mobility challenges of today and tomorrow. We design and manufacture a complete range of transportation systems, from high-speed trains to electric buses and driverless trains, as well as infrastructure, signalling and digital mobility solutions. Joining us means joining a truly global community of more than 75 000 people dedicated to solving real-world mobility challenges and achieving international projects with sustainable local impact. INTRODUCTION Alstom has been part of the Belgian railway history for about 130 years. Today, from Charleroi (BE), the company is active through two centers of excellence: Signalling Systems – Center of excellence ERTMS(European standard development and implementation) Power Electronics – Center of excellence Traction Systems (Traction solutions / auxiliary converters / low voltage cabinets) Important efforts in R&D support the development of these activities contributing actively to promoting a safe and performant railway network as well as sustainable mobility solutions worldwide. The Alstom Belgium teams have an excellent knowledge and reputation in the global project management and every day from Charleroi, about 1050 employees, among which 500 engineers, are working on more than 100 projects all over the world. Thanks to them, the site of Charleroi makes a significant contribution to worldwide rail transportation development. POSITION OVERVIEW: As Project Manager, you will have to: deliver projects according to QCD commitments of the baseline sold; serve clients and propose additional services to make business grow; Network and links The job holder reports directly to the Customer Services Business Director. The job holder will functionally manage and coordinate the Project Core Team: Project Engineering Manager (PrEM), Project Planning Manager (PrPM), Project Industrial and Sourcing Manager (PrISM), Project Financial Manager (PrFM), Project Warranty Manager (PWM), Project Quality and Safety Manager (PrQSM). The job holder will be Alstom’s point of contact for his/her customers of the Railway Industry. MISSION : For several projects at the same time, the Project Manager is in charge to: Deliver project according to QCD commitments as specified at contract signature; Enroll, manage and obtain the commitments of each member the Project Core Team; Support Customer Director in proposing and negotiating variation orders with customer; Act in respect of applicable process and standards, and support the mission of the Project Quality and Safety Manager; Set up organisational and behaviour rules and pilot planning and resources to meet customers’ needs; Demonstrate performance in : Scope Management Time Management Cost Management Resources Management Risk and Opportunities identification and Management Quality Management Communication Manage Report to Customer Services Business Director weekly updates and contributes to the consolidation of project reporting (project dashboard and project indicators). Medium/Long term generic objectives: Contribute to build on return of experience in order to: Improve the operational reliability Give feedback to the Tender team about the reliability of costing Allow the set-up of predictive maintenance Develop customer portfolio by proposing spontaneous offers and services adapted SKILLS & EDUCATION Education: Engineering Degree (Master equivalent or above) in one or more of the following fields: Industrial, Telecom, Electrical, Electronics, Automation. Desired knowledge / Experience: Minimum of 5 years’ experience of managing high value or technically complex projects in the Railway Automobile and/or Aeronautic Industry Experience in international projects and openness to multi-cultural environment Key Knowledge Areas: Deep understanding of technical/engineering requirements and product specifications Good control of contractual, financial and political stakes Team management excellence: to enrol & motivate internal and external partners Strong analytical and synthesis skills Resilience to cope with complex problems involving several technologies Experience of working in a matrix organisation Effective active listening and communication skills Technical skills and Competencies Strong leadership Results focused Rigor pragmatism and discipline (stick to deadlines) Excellent interpersonal skills to fulfil role of interface manager with the customers and Project Core Team Members Learning fast, quick understanding of new technologies Windows, SAP and Asset Management software knowledge Language skills: Fluency in French, English. Dutch is a plus. The job is located in Charleroi (Belgium). Travels about 20% of time. An agile, inclusive and responsible culture is the foundation of our company where diverse people are offered excellent opportunities to grow, learn and advance in their careers. We are committed to encouraging our employees to reach their full potential, while valuing and respecting them as individuals. Job Type:​Experienced​
Project Manager Services
Alstom, Charleroi, Walloon Region, be
Req ID:96973 Nous créons des innovations intelligentes pour relever les défis de la mobilité d’aujourd'hui et de demain. Nous concevons et fabriquons une gamme complète de systèmes de transport, des trains à grande vitesse aux bus électriques et trains sans conducteur, en passant par les solutions d'infrastructure, de signalisation et de mobilité digitale. Nous rejoindre, c’est intégrer une communauté internationale de plus 75000 personnes qui se consacrent à la résolution de problèmes de mobilité concrets et à la réalisation de projets internationaux ayant un impact local durable. INTRODUCTION Alstom has been part of the Belgian railway history for about 130 years. Today, from Charleroi (BE), the company is active through two centers of excellence: Signalling Systems – Center of excellence ERTMS(European standard development and implementation) Power Electronics – Center of excellence Traction Systems (Traction solutions / auxiliary converters / low voltage cabinets) Important efforts in R&D support the development of these activities contributing actively to promoting a safe and performant railway network as well as sustainable mobility solutions worldwide. The Alstom Belgium teams have an excellent knowledge and reputation in the global project management and every day from Charleroi, about 1050 employees, among which 500 engineers, are working on more than 100 projects all over the world. Thanks to them, the site of Charleroi makes a significant contribution to worldwide rail transportation development. POSITION OVERVIEW: As Project Manager, you will have to: deliver projects according to QCD commitments of the baseline sold; serve clients and propose additional services to make business grow; Network and links The job holder reports directly to the Customer Services Business Director. The job holder will functionally manage and coordinate the Project Core Team: Project Engineering Manager (PrEM), Project Planning Manager (PrPM), Project Industrial and Sourcing Manager (PrISM), Project Financial Manager (PrFM), Project Warranty Manager (PWM), Project Quality and Safety Manager (PrQSM). The job holder will be Alstom’s point of contact for his/her customers of the Railway Industry. MISSION : For several projects at the same time, the Project Manager is in charge to: Deliver project according to QCD commitments as specified at contract signature; Enroll, manage and obtain the commitments of each member the Project Core Team; Support Customer Director in proposing and negotiating variation orders with customer; Act in respect of applicable process and standards, and support the mission of the Project Quality and Safety Manager; Set up organisational and behaviour rules and pilot planning and resources to meet customers’ needs; Demonstrate performance in : Scope Management Time Management Cost Management Resources Management Risk and Opportunities identification and Management Quality Management Communication Manage Report to Customer Services Business Director weekly updates and contributes to the consolidation of project reporting (project dashboard and project indicators). Medium/Long term generic objectives: Contribute to build on return of experience in order to: Improve the operational reliability Give feedback to the Tender team about the reliability of costing Allow the set-up of predictive maintenance Develop customer portfolio by proposing spontaneous offers and services adapted SKILLS & EDUCATION Education: Engineering Degree (Master equivalent or above) in one or more of the following fields: Industrial, Telecom, Electrical, Electronics, Automation. Desired knowledge / Experience: Minimum of 5 years’ experience of managing high value or technically complex projects in the Railway Automobile and/or Aeronautic Industry Experience in international projects and openness to multi-cultural environment Key Knowledge Areas: Deep understanding of technical/engineering requirements and product specifications Good control of contractual, financial and political stakes Team management excellence: to enrol & motivate internal and external partners Strong analytical and synthesis skills Resilience to cope with complex problems involving several technologies Experience of working in a matrix organisation Effective active listening and communication skills Technical skills and Competencies Strong leadership Results focused Rigor pragmatism and discipline (stick to deadlines) Excellent interpersonal skills to fulfil role of interface manager with the customers and Project Core Team Members Learning fast, quick understanding of new technologies Windows, SAP and Asset Management software knowledge Language skills: Fluency in French, English. Dutch is a plus. The job is located in Charleroi (Belgium). Travels about 20% of time. Les engagements de notre entreprise se fondent sur une culture agile, inclusive et responsable qui offre à des personnes de tout horizon l’opportunité de se développer, d’apprendre et de progresser tout au long de leur carrière. Nous encourageons nos salariés à réaliser pleinement leur potentiel, tout en leur accordant l’estime et le respect dus à chaque individu. Job Type:​Expérimenté
Project Manager Services
Alstom, Charleroi, Wallonia
Req ID:96973 We create smart innovations to meet the mobility challenges of today and tomorrow. We design and manufacture a complete range of transportation systems, from high-speed trains to electric buses and driverless trains, as well as infrastructure, signalling and digital mobility solutions. Joining us means joining a truly global community of more than 75 000 people dedicated to solving real-world mobility challenges and achieving international projects with sustainable local impact. INTRODUCTION Alstom has been part of the Belgian railway history for about 130 years.Today, from Charleroi (BE), the company is active through two centers of excellence:Signalling Systems – Center of excellence ERTMS(European standard development and implementation)Power Electronics – Center of excellence Traction Systems (Traction solutions / auxiliary converters / low voltage cabinets)Important efforts in R&D support the development of these activities contributing actively to promoting a safe and performant railway network as well as sustainable mobility solutions worldwide.The Alstom Belgium teams have an excellent knowledge and reputation in the global project management and every day from Charleroi, about 1050 employees, among which 500 engineers, are working on more than 100 projects all over the world. Thanks to them, the site of Charleroi makes a significant contribution to worldwide rail transportation development.POSITION OVERVIEW:As Project Manager, you will have to:deliver projects according to QCD commitments of the baseline sold;serve clients and propose additional services to make business grow;Network and linksThe job holder reports directly to the Customer Services Business Director.The job holder will functionally manage and coordinate the Project Core Team: Project Engineering Manager (PrEM), Project Planning Manager (PrPM), Project Industrial and Sourcing Manager (PrISM), Project Financial Manager (PrFM), Project Warranty Manager (PWM), Project Quality and Safety Manager (PrQSM).The job holder will be Alstom’s point of contact for his/her customers of the Railway Industry.MISSION :For several projects at the same time, the Project Manager is in charge to:Deliver project according to QCD commitments as specified at contract signature;Enroll, manage and obtain the commitments of each member the Project Core Team;Support Customer Director in proposing and negotiating variation orders with customer;Act in respect of applicable process and standards, and support the mission of the Project Quality and Safety Manager;Set up organisational and behaviour rules and pilot planning and resources to meet customers’ needs;Demonstrate performance in : Scope Management Time Management Cost Management Resources Management Risk and Opportunities identification and Management Quality Management Communication Manage Report to Customer Services Business Director weekly updates and contributes to the consolidation of project reporting (project dashboard and project indicators). Medium/Long term generic objectives:Contribute to build on return of experience in order to:Improve the operational reliabilityGive feedback to the Tender team about the reliability of costingAllow the set-up of predictive maintenanceDevelop customer portfolio by proposing spontaneous offers and services adaptedSKILLS & EDUCATION Education: Engineering Degree (Master equivalent or above) in one or more of the following fields: Industrial, Telecom, Electrical, Electronics, Automation.Desired knowledge / Experience:Minimum of 5 years’ experience of managing high value or technically complex projects in the Railway Automobile and/or Aeronautic IndustryExperience in international projects and openness to multi-cultural environmentKey Knowledge Areas: Deep understanding of technical/engineering requirements and product specifications Good control of contractual, financial and political stakes Team management excellence: to enrol & motivate internal and external partners Strong analytical and synthesis skills Resilience to cope with complex problems involving several technologies Experience of working in a matrix organisation Effective active listening and communication skills Technical skills and CompetenciesStrong leadershipResults focusedRigor pragmatism and discipline (stick to deadlines)Excellent interpersonal skills to fulfil role of interface manager with the customers and Project Core Team MembersLearning fast, quick understanding of new technologiesWindows, SAP and Asset Management software knowledge Language skills: Fluency in French, English. Dutch is a plus.The job is located in Charleroi (Belgium). Travels about 20% of time.An agile, inclusive and responsible culture is the foundation of our company where diverse people are offered excellent opportunities to grow, learn and advance in their careers. We are committed to encouraging our employees to reach their full potential, while valuing and respecting them as individuals. Job Type:​Experienced​
Manager, Maintenance
GSK, Wavre, Walloon Region, be
We are looking to recruit a Maintenance Manager, for the Manufacturing Prodcution Unit LVV, in Wavre.Your responsibilities:You ensure preventive, curative and modificative maintenance program of Stream equipment’s and buildings in order to make sure of their maximum availability. In this frame, you organize and monitor performance indicators. You ensure the full responsibility of a maintenance team (12 to 15 people). This includes people selection, supervisors' coaching, foremen coaching, personnel training to the required competencies, planning’s' management, the elaboration and management of operating and investment budgets, contacts with social partners, as well as all daily aspects of a team's life. You make sure that cGMP (current Good Manufacturing Practices), GMP procedures and recommendations from the authorities are respected. You manage and document deviations by integrating changes to maintenance operations. You play a key role in the cross-discipline effort by providing technical support to the deviation handling process (Root causes identification and selection of CAPAs in order to avoid recurrence of deviation with technical root causes). You actively participate in external audits and their preparation. You represent stream maintenance in front of auditors. You resolve audit actions. You make sure that EHS standards and policies are respected. You coordinate the setting in legal conformity of stream equipment’s. You are accountable for the technical areas of your stream in terms of housekeeping and personnel access. You maintain good maintenance practices by updating our procedures and the checklists associated to them. You ensure redaction, training and follow-up of the procedures. You bring technical support for the stream on various technical problems and in the frame of new projects. You follow strategic projects as maintenance responsible for the stream. You manage improvement projects (design, construction, implementation, validation) and ensure a technological watch of new technologies. You coordinate the entire CAPEX budgets of the Stream. You act as the stream representative for the local Technical Services. You manage transversal improvement projects for the stream Why you?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:Industrial/civil engineer degree, or equivalent experienceAt least 8 years of experience, with proven experience in Technical Services & People ManagementFluent in French and English (written and spoken)Strong EHS MindsetPreferred Qualifications:If you have the following characteristics it would be a plus:Effective communication skills, including presentation skillsHigh level of resilienceSense of urgency, flexibility and accountabilityProven Planning & Organizational skills Analytical (Troubleshooting) & Problem-solving skills to manage operations and related budgetAbility to maintain attention to detail, while completing multiple or repetitive tasksStrong quality mindset –demonstrate a serious commitment to accuracy and quality while meeting goals or deadlines
Manager, CMC Vaccines Mature Products, Regulatory Affairs
GSK, Wavre, Walloon Region, be
Manager, CMC Vaccines Mature ProjectsYour responsibilities:You drive the CMC strategy, coordinate the timely preparation and authors, as needed, technical (CMC) regulatory documents to support development and registration of new vaccines or lifecycle activities and maintenance of registered vaccines, in accordance with the applicable regulatory & scientific standards, taking into account the evolving regulatory requirements.You provide regulatory advice and guidance to the Technical Development Team and/or Technical Life-Cycle Team (TLCT), Implementation Committee, Specification Review Committee, Technical Review Board, CMC Expert Panel, and provides regulatory support to their partners in R&D, Quality Control, Manufacturing, QA and Supply. You ensure adequate interaction and partnership with the Global Regulatory Lead’s team in order to define proper regulatory CMC filing strategy.You ensure adequate contribution during interactions with Worldwide regulatory authorities. You ensure, in a continuous improvement mindset, regulatory compliance is maintained and shares best-practices and learnings within the CMC Regulatory teams and other impacted functions. You may engage and lead CMC Subject Matter Expert activities, both internally (for increased compliance, harmonisation and efficiency) and externally (external advocacy and shaping the regulatory environment).You may mentor or train staff.You may participate in corporate evaluation and provide CMC regulatory support/advice to in-licensing and divestment projects.You may deliver CMC regulatory strategy to support major inspections (eg PAI's) or quality incidents (PIRCs).Why you?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:Bachelor’s degree in Sciences or Medical Sciences with relevanr experienceSuccessfully managed multiple projects simultaneously.Sound knowledge of drug development and manufacturing and supply processes and may have a specialized area of expertise.Knowledge of CMC regulatory requirements. Demonstrated ability to handle global CMC issues through continuous change and improvementStrong communication skillsFluent in EnglishPreferred Qualifications:If you have the following characteristics it would be a plus:Master’s degree or above in Chemistry, pharmacy, biological or closely related science advanced degree.Regulatory Affairs Certification (e.g. RAPS).Experience in Pharmaceutical industry or Research organizations, established in Regulatory Affairs and with demonstrated experience of leadership in a matrix environment.Sound knowledge of vaccines/biological products development, manufacturing and supply processes.Continued professional growth in global regulatory affairs including communication of evolving/emerging trends and policies. Has identified opportunities to further educate colleagues and formulate approaches to most effectively meet new requirements.Identified as CMC Regulatory expert in a specific subject area.Highly developed interpersonal, presentation and communication skills.Proven experience in training staff within an organisation.*Li-GSK
Assistant Store Manager (H/F) - Région de Mons
Accent, Mons, Henegouwen, BE
Functieomschrijving En tant que bras droit du Store Manager, vous connaissez les tenants et les aboutissants du magasin comme votre poche. Avec le Store Manager, vous avez pour mission d'amener le magasin à un niveau encore plus élevé. Vous inspirez les personnes qui vous entourent et aidez l'équipe au quotidien.•Vous avez une attitude commerciale et savez la transmettre.•Vous gardez les objectifs à l'esprit, en vous efforçant toujours d'obtenir les meilleures performances.•Vous donnez systématiquement du feedback•Vous avez l'esprit d'équipe et êtes un exemple•Vous recherchez activement des solutions et élaborez des plans d'action après discussion avec le Store Manager.•En collaboration avec le Store Manager, vous veillez à ce que le magasin soit organisé de manière efficace et conforme à l'ADN de l'organisation.•Vous optimisez les processus et réfléchissez avec nous à la manière dont vous pouvez influencer les indicateurs clés de performance de manière intelligente.•Vous rendez compte au Store Manager et le remplacez en son absence.Jouw profiel •Vous êtes un polyvalent, flexible et commercial.•Vous êtes orienté résultats et solutions.•Vous êtes un leader enthousiaste qui ne recule pas devant un défi.•Vous avez une expérience probante dans le domaine de la vente au détail.•Vous aimez travailler le samedi (1 jour de récupération par semaine). Wij bieden jou •Un travail varié avec beaucoup d'autonomie et de responsabilités.•Un package salarial fixe et variable compétitif, complété par des extra légaux•Des opportunités de carrière basées sur des résultats et des compétences avérésBedrijfsinformatie Notre client est un des leaders de la vente de smartphones, pc, tablettes et accessoires. Leurs dynamiques collaborateurs mettent tout en oeuvre pour accompagner les clients dans leurs achats.Accent Jobs allie la flexibilité d’une agence d’intérim et la qualité d’une agence de sélection.Seuls des emplois pouvant déboucher sur un contrat fixe sont proposés. Pour ce faire, nous pouvons nous appuyer sur 700 collaborateurs passionnés qui aident chaque jour plus de 12 000 personnes à trouver un emploi.Comptant 230 agences, Accent Jobs constitue le plus grand réseau de la Belgique. Erkenningsnummer: W.INT.040 Diversiteit en inclusie zijn belangrijk voor Accent. Wie, wat of hoe je ook bent of waar je voor staat, het zijn jouw talenten die het verschil maken.
Manager Consultance
UCM, Namur, Walloon Region, be
Jobs Date de dernière mise à jour : 11/05/2021 UCM est la principale organisation patronale francophone engagée audacieusement dans la défense des indépendants et des chefs d'entreprises.  Active en Wallonie et à Bruxelles, UCM compte près de 900 collaborateurs, passionnés par leur travail et spécialisés dans une gamme toujours plus large de services, tels que : l’accompagnement à la création d'entreprises  le guichet d'entreprises  la caisse d'assurances sociales  le secrétariat social  la caisse d'allocations familiales. Stage Malheureusement, au vu la situation exceptionnelle que nous traversons, nous ne sommes pas en mesure d’accueillir des stagiaires durant cette année scolaire 2020-2021. Ce n’est que partie remise, à bientôt ! Candidature spontanée Nous t'invitons également à envoyer ta candidature de façon spontanée en t'inscrivant . Attention, ce formulaire ne concerne que les demandes d'emploi. Une culture mobilisante C’est avec dynamisme et enthousiasme que nous défendons les intérêts des indépendants et entrepreneurs. Une orientation client Chaque indépendant, chaque entrepreneur est unique, nous sommes à l’écoute de ses besoins, nous le conseillons et nous pensons en termes de solutions. Une expertise technique En général universitaires (droit, sciences du travail...) ou gradués (droit, GRH ou conseiller social et fiscal...), nous avons tous acquis une parfaite maîtrise technique dans notre domaine d’activités : organisation patronale, lois sociales, allocations familiales, secrétariat social, conseil en création ou transfert d’entreprise. Partagez
Manager Business Analytics (H/F)
Actief Interim, Charleroi, Walloon Region, be
Pour l'un de nos clients actif dans le secteur des Telecoms, nous recherchons un manager business analytics (h/f) pour assurer les tâches suivantes:Team management: ·Encadrer, motiver et évaluer lescollaborateurs de la cellule et prendre les mesures correctrices qui s'imposenten cas de niveau de compétence/motivation insuffisant Assurer ledéveloppement des compétences et des connaissances des collaborateursainsi que la formation continue sur le terrain Fournir auxcollaborateurs toutes les explications détaillées relatives aux différentsmétiers Etre ouvert aux idéespouvant venir des collaborateurs Remonter les conflitset les problèmes au N+1 Organiser et coordonnerle travail des différentes cellules (absences, réunions, formations, …) Gestionopérationnelle de la cellule :Surveiller l’étatd’avancement des projets mais surtout créer les instruments nécessaires aupilotage du projet. Assurerl’organisation et l’efficacité des formations de la division BackOfficeSurveiller et analyserles systèmes d'information et de données, évaluer leurs performances etdécouvrir des façons de les renforcer (nouvelles technologies, mises àniveau, etc.)Concevoir et mettre enœuvre des procédures efficaces et sûres pour la manipulation et l'analysedes données avec une attention à tous les aspects techniquesResponsable de lacoordination des partenaires externesMaintenance des diversoutils nécessaires aux activités Fournir des tableauxde bord et reporting permettant la prise de décision afin d’assurerl’atteinte des objectifs opérationnels et de rentabilité au sein dudépartement Wat wij van jou vragen:Qualifications attendues:·Vous avezun Master en commerce ou en finance (contrôleur de gestion)mais la compréhension des deux univers estcapitale pour exercer ce métier.·Expériencede plus de 5 ans dans le domaine.·Parfaitemaitrise des outils Microsoft (Excel, Access, Word, Powerpoint, Outlook, VBA,Tableau) et trèsbonnes connaissances de SAP· Langues : Français – AnglaisSoftskills·Vous êtesdoté de réelles qualités de gestion et êtes capable d’influer le comportementdes collaborateurs. ·Vous êtescapable de motiver votre équipe.·Vous avezune attitude positive et de l’empathie.·Vousaimez les relations interpersonnelles.·Vous êtesflexible et ouvert aux changements et aux améliorations.·Voussavez faire preuve d’innovationWat wij jou bieden:CDI, temps pleinSalaire selon expérience
Manager Production (Week/Night)
GSK, Wavre, Walloon Region, be
The Team: To join Nicolas and his brilliant team. Nicolas 'team (12) is dedicated to the production of Pertussis acellular antigens. You report directly to Nicolas, Head of Production Downstream.This is a full-time, permanent role (CDI) based in Wavre, Belgium (no relocation support provided).Work timetables: From Sunday 10 PM (22h) to Monday 6 AM (6h)Job purpose: You are responsible for the transversal operations of a Production Unit within a production plant during night shift. You report into the Head of Manufacturing.Your responsibilities:In this role you ensure:Manufacturing plan is followed and delivered with a safety and quality culture focusTransversal management of manufacturing activities, logistic and process, during night shift (fermentation, purification, detoxification, etc.)Management of manufacturing events (deviation, CAPA, etc.) and provide support to the teamsAdequate communication between the different shiftsManagement and development of a team of Blue and White collarsWhy you?Basic Qualifications:We are looking for professionals with the following required skills to achieve our goals (must-have): Master’s degree level with Scientific orientationProven successful experience in People ManagementMust be fluent in French with a good command of EnglishEffective communicationPlan & organizeSet direction, inspire, engage and develop.*LIPreferred Qualifications:The following characteristics are assets (nice-to-have):One year of experience in a similar roleAutonomous and accountableRigorous and disciplinedFlexible
Manager, Sterility Assurance
GSK, Wavre, Wallonia
Mar 15 2021As Manager Sterility Assurance, you provide support and expertise to the operations and Sterility assurance manager to ensure that the Manufacturing Performance Unit applies all Sterility Assurance processes (including Aseptic Practices, Environmental Monitoring, Cleaning and Sanitization, Sterilization, Media Form and Fill) to confidently deliver products to patients with the highest sterility assurance level at an appropriate cost.You are the subject matter expert for production – MPU OneRix and contribute as a member of the expertise network to the harmonization and continuous improvement of sterility assurance knowledge and practices across GSK Vaccines Your responsibilities:Sterility Assurance (EM, Cleaning, Sanitization, sterilization) You are the key contact for OneRix Production for all matters related to Sterility Assurance including Aseptic Practices, Environmental monitoring, for clean rooms (viable and non-viable) operators and critical utilities, Surface Cleaning and Sanitization, Sterilization, Media Fill and Sterility Failures You support production and QA for investigations and deviations You support production to put in place the right Level of environmental monitoring You challenge technical and scientific aspects of facilities design and aseptic principles with Production, Technical Services and QA. You approve scientific and technical reports (test procedure, validation report, scientific report, deviations reports) You support production to maintain the cGMPs in the area of responsibility (SOP, documentation, audits, training, method validation) You support the implementation of adequate training for aseptic gowning and practices and sterility assurance, including shop floor mentoring as required Why you? Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:Master’s degree in sciences (Bio Engineering, Biology, Biotechnology,Pharmacology, …) or equivalent experience.At least 5 years professional experience in the pharmaceutical / biotech /medical device / food industry or equivalent environment, including at least 3 years of proven aseptic manufacturing.Direct experience with GxP regulated environmentProven experience in Quality Assurance, not necessarily within a quality department.Preferred Qualifications:If you have the following characteristics it would be a plus:Aseptic manufacturing and environmental monitoring are critical domainsrequiring a high level of expertiseA strong knowledge of technology, product, processes is required toobtain the right level of influence, credibility and decision making
Manager Quality Control
GSK, Wavre, Wallonia
As a Quality Control Direct Manager, you will supervise daily a team of Quality Control Laboratory Technicians in a multiple products environment and be an expert in his field.Job Purpose:Guarantee results delivery according to standard lead-time with compliance regarding quality and EHS requirements, and in alignment with QA partner.Be accountable for capacity risk assessments (people/equipment/change control) and will propose solutions/mitigations with other QC partners (ex: infrastructure, lab support, …) or proactively escalate blocking points.Be responsible for managing change (organization, capacity, process, mindset, within his/her team) is a key success factor (ex: implementation of digital solutions, lean-lab, automation, TroubleshootingContribute to the scientific and technical assay strategy, design and optimization in agreement with pharmacopeia, CAP and GMP requirementsSupport root cause analyzes and troubleshooting activities and innovative TechnologiesCould coordinate testing activities for the QC department in agreement to GMP requirementsYour Responsibilities:Motivate and encourage a team of Technicians to achieve maximum productivity with good management of priorities and team well-being.Provide technical support to your direct reports.Organize and monitor the performance progress efficiency of the team through performance indicators related to Safety, Quality, Supply, Cost for example.Escalate proactively risks & problems and propose solutions.Ensure compliance of the operations with GMP and Authorities requirements in collaboration with QA.Develop your team and act as a coach for them.Anticipate potential improvements, implementation of corrective and preventive actions. You will also be responsible to drive continuous improvement in the team.Fulfill the role of a subject matter expert for assays, set up and oversight assays required to release GSK Vaccines. Develop technology and scientific expertise of the platform through participation to scientific meetings and congresses. Provide scientific coaching/training to other scientists and supervisors.Provide support for the development and/or review of internal and external publications, technical documents and communications.Be the technical reference for scientific and technical activities (internal and external): – internal activities related to assay development and validation, assay maintenance and testing performed under its responsibility.Participate to the follow up of collaborations with other teams/experts to share/gain scientific and technical expertise and for technology transfer within and outside GSK VaccinesParticipate to QC knowledge management in the field of expertise.Why You?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:You hold a Scientific University Deree or equivalent scientific background.Practical and theoretical knowledge in the domain of laboratory activity (eg. Biochemistry, Virology,…)You have proven experience of leading and managing a lab team.You have at least 10 years of professional experience including at least 8 years of relevant experience preferably within R&D, GIO/Q or similar roles in Pharma industry.You have a strong knowledge of international regulatory requirements that apply to vaccines (and beyond to manufacturing) and in depth knowledge of cGMP.You are a strong collaborator with ability to influence, to work in project teams in a multidisciplinary environment and a matrix organization and to work effectively across boundariesYou have the ability to develop a strong vision, and set direction in this domain, while being inspiring, and having a positive and optimistic attitude in managing day-to-day activities.Relevant experience in change management, project management and lean management could be an advantage.You are bi-lingual French/English, written competencies in EnglishPreferred Qualifications:If you have the following characteristics, it would be a plus:Good communication skillsAutonomousHands-on mentalityContinuous Improvement Mindset
Manager Quality Control
GSK, Wavre, Wallonia
Job Purpose:Guarantee results delivery according to standard lead-time with compliance regarding quality and EHS requirements, and in alignment with QA partner.Be accountable for capacity risk assessments (people/equipment/change control) and will propose solutions/mitigations with other QC partners (ex: infrastructure, lab support, …) or proactively escalate blocking points.Be responsible for managing change (organization, capacity, process, mindset, within his/her team) is a key success factor (ex: implementation of digital solutions, lean-lab, automation, TroubleshootingContribute to the scientific and technical assay strategy, design and optimization in agreement with pharmacopeia, CAP and GMP requirementsSupport root cause analyzes and troubleshooting activities and innovative TechnologiesCould coordinate testing activities for the QC department in agreement to GMP requirementsYour Responsibilities:Motivate and encourage a team of Technicians to achieve maximum productivity with good management of priorities and team well-being.Provide technical support to your direct reports.Organize and monitor the performance progress efficiency of the team through performance indicators related to Safety, Quality, Supply, Cost for example.Escalate proactively risks & problems and propose solutions.Ensure compliance of the operations with GMP and Authorities requirements in collaboration with QA.Develop your team and act as a coach for them.Anticipate potential improvements, implementation of corrective and preventive actions. You will also be responsible to drive continuous improvement in the team.Fulfill the role of a subject matter expert for assays, set up and oversight assays required to release GSK Vaccines. Develop technology and scientific expertise of the platform through participation to scientific meetings and congresses. Provide scientific coaching/training to other scientists and supervisors.Provide support for the development and/or review of internal and external publications, technical documents and communications.Be the technical reference for scientific and technical activities (internal and external): – internal activities related to assay development and validation, assay maintenance and testing performed under its responsibility.Participate to the follow up of collaborations with other teams/experts to share/gain scientific and technical expertise and for technology transfer within and outside GSK VaccinesParticipate to QC knowledge management in the field of expertise.Why You?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:You hold a Scientific University Deree or equivalent scientific background.Practical and theoretical knowledge in the domain of laboratory activity (eg. Biochemistry, Virology,…)You have proven experience of leading and managing a lab team.You have at least 10 years of professional experience including at least 8 years of relevant experience preferably within R&D, GIO/Q or similar roles in Pharma industry.You have a strong knowledge of international regulatory requirements that apply to vaccines (and beyond to manufacturing) and in depth knowledge of cGMP.You are a strong collaborator with ability to influence, to work in project teams in a multidisciplinary environment and a matrix organization and to work effectively across boundariesYou have the ability to develop a strong vision, and set direction in this domain, while being inspiring, and having a positive and optimistic attitude in managing day-to-day activities.Relevant experience in change management, project management and lean management could be an advantage.You are bi-lingual French/English, written competencies in EnglishPreferred Qualifications:If you have the following characteristics, it would be a plus:Good communication skillsAutonomousHands-on mentalityContinuous Improvement Mindset
Manager qualité
IMPACT Nivelles, Wallonia
L’EntreprisePour un de nos clients actifs dans le secteur du transport et de la logistique, nous sommes actuellement à la recherche d'un.e Manager qualité. Le PosteVotre fonction :Vous travaillerez au seind'une société familiale réputée dans le transport et la logistique Vous assurez la conformité du système de management vis-à-vis des normes ISO 9001 Vous veillez à la conformité du système documentaire de l'ensemble des processus qualité Vous gérez quotidiennement les tâches du département qualité ainsi que le calendrier des audits internes et externes Vous collaborez étroitement avec les services achats et ordonnancement, les services BE, méthodes et production ainsi qu'avec le service commercial Le ProfilVotre profil :Vous possédez idéalement un master / ingéniorat industriel avec formation en qualité Vous êtes expérimenté(e) Vous possédez un véhicule personnel Vous êtes flexible au nouveau des horaires Vous êtes précis, rigoureux et possédez un esprit d'analyse et sens critique  L'offreNous vous offrons un contrat d'intérim en vue d'engagement dans une entreprise familiale et florissante de la région de Tubize.
Manager de l’équipe des Analystes et Architecte fonctionnel
UCM, Namur, Wallonia
Jobs Date de dernière mise à jour : 30/03/2021 UCM est la principale organisation patronale francophone engagée audacieusement dans la défense des indépendants et des chefs d'entreprises.  Active en Wallonie et à Bruxelles, UCM compte près de 900 collaborateurs, passionnés par leur travail et spécialisés dans une gamme toujours plus large de services, tels que : l’accompagnement à la création d'entreprises  le guichet d'entreprises  la caisse d'assurances sociales  le secrétariat social  la caisse d'allocations familiales. Stage Malheureusement, au vu la situation exceptionnelle que nous traversons, nous ne sommes pas en mesure d’accueillir des stagiaires durant cette année scolaire 2020-2021. Ce n’est que partie remise, à bientôt ! Candidature spontanée Nous t'invitons également à envoyer ta candidature de façon spontanée en t'inscrivant . Attention, ce formulaire ne concerne que les demandes d'emploi. Une culture mobilisante C’est avec dynamisme et enthousiasme que nous défendons les intérêts des indépendants et entrepreneurs. Une orientation client Chaque indépendant, chaque entrepreneur est unique, nous sommes à l’écoute de ses besoins, nous le conseillons et nous pensons en termes de solutions. Une expertise technique En général universitaires (droit, sciences du travail...) ou gradués (droit, GRH ou conseiller social et fiscal...), nous avons tous acquis une parfaite maîtrise technique dans notre domaine d’activités : organisation patronale, lois sociales, allocations familiales, secrétariat social, conseil en création ou transfert d’entreprise. Partagez
Manager qualité
IMPACT Fleurus, Tubize, Wallonia
L’EntreprisePour un de nos clients actifs dans le secteur du transport et de la logistique, nous sommes actuellement à la recherche d'un.e Manager qualité. Le PosteVotre fonction :Vous travaillerez au seind'une société familiale réputée dans le transport et la logistique  Vous assurez la conformité du système de management vis-à-vis des normes ISO 9001 Vous veillez à la conformité du système documentaire de l'ensemble des processus qualité Vous gérez quotidiennement les tâches du département qualité ainsi que le calendrier des audits internes et externes Vous collaborez étroitement avec les services achats et ordonnancement, les services BE, méthodes et production ainsi qu'avec le service commercial Le ProfilVotre profil :Vous possédez idéalement un master / ingéniorat industriel avec formation en qualité Vous êtes expérimenté(e) Vous possédez un véhicule personnel Vous êtes flexible au nouveau des horaires Vous êtes précis, rigoureux et possédez un esprit d'analyse et sens critique  L'offreNous vous offrons un contrat d'intérim en vue d'engagement dans une entreprise familiale et florissante de la région de Tubize.
Manager qualité
IMPACT, Wallonia
JobomschrijvingVotre fonction :Vous travaillerez au seind'une société familiale réputée dans le transport et la logistique Vous assurez la conformité du système de management vis-à-vis des normes ISO 9001Vous veillez à la conformité du système documentaire de l'ensemble des processus qualitéVous gérez quotidiennement les tâches du département qualité ainsi que le calendrier des audits internes et externesVous collaborez étroitement avec les services achats et ordonnancement, les services BE, méthodes et production ainsi qu'avec le service commercialGewenst profielVotre profil :Vous possédez idéalement un master / ingéniorat industriel avec formation en qualitéVous êtes expérimenté(e)Vous possédez un véhicule personnelVous êtes flexible au nouveau des horairesVous êtes précis, rigoureux et possédez un esprit d'analyse et sens critique AanbodNous vous offrons un contrat d'intérim en vue d'engagement dans une entreprise familiale et florissante de la région de Tubize.