production quality assurance jobs

30Jobs Found

30 jobs found for production quality assurance jobs

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Medical Device Specialist H/F

EyeDPharma

Liège, Liège
11 days ago
Liège, Liège
11 days ago

Pour soutenir son développement, EyeD Pharma recherche un Medical Device Specialist.

Fonction

  • Vous êtes en charge du développement des dispositifs médicaux
  • Vous fournissez une expertise technique dans les domaines suivants :
    1. Définition des Design Inputs
    2. Planification et exécution des études nécessaires à l’établissement des Design Outputs
    3. Mise en place de la stratégie de vérification et de validation et suivi de son exécution
    4. Mise en place et exécution de la stratégie de gestion des risques liés aux produits
  • Vous êtes familier avec les outils de Quality-by-Design et les appliquer adéquatement
  • Vous coordonnez et supervisez les activités réalisées par les sous-traitants
  • Vous êtes responsable de la constitution de la documentation technique
  • Vous garantissez la conformité aux procédures d'exploitation standard et aux exigences réglementaires pour les produits combinés selon les normes européennes et américaines
  • Vous collaborez de manière constructive et bienveillante avec chaque membre du personnel impliqués dans le projet (contrôle qualité, assurance qualité, CMC, production, RA, etc)
  • Vous réalisez des expériences appropriées pour résoudre les problèmes techniques et réduire les risques
  • Vous gérez de manière efficace et cohérente vos projets

Mots clés : medical device, ophthalmology, development, pharmaceutical, ocular pathologies, research scientist, quality, drug product, chemistry, chemical, life sciences, sciences appliqués, innovation, technical documentation, MDR, GSPR, design control, dispositifs médicaux, research scientist, ISO14971, ISO13485, Risk management, Verification and validation (V&V)

Profil

  • Vous avez un minimum de 3 ans d'expérience dans l'industrie pharmaceutique et plus précisément dans les dispositifs médicaux
  • Vous avez un diplôme universitaire en sciences appliquées, de préférence en génie chimique ou biomédical, en sciences pharmaceutiques ou en chimie des polymères
  • Vous avez une expérience dans le développement de dispositifs médicaux
  • Vous avez une expérience en matière de gestion des risques liés à la qualité (ISO 14971 ; ICH Q9)
  • Une expérience dans le domaine des systèmes d'administration de médicaments basés sur la technologie des polymères est un plus
  • Des compétences avérées en matière de gestion de projets sont un atout.
  • Vous avez de très bonnes connaissances des exigences en termes de réglementation de développement des dispositifs médicaux (MDR, ISO 13485)
  • Vous parlez couramment l'anglais et le français
  • Vous avez une excellente communication écrite et oral dans les deux langues et vous échangez avec beaucoup de bienveillance avec vos collègues
  • Vous faites preuve d’esprit d’équipe, d’une attitude proactive et vous êtes disposé(e) à travailler dans un environnement « start-up »

Offre

EyeD Pharma vous propose un CDI, à temps plein, dans un environnement de travail convivial avec des projets passionnants et innovants.

« Profile Group gère cette mission en exclusivité. Tout candidat intéressé est donc invité à postuler exclusivement via cette annonce (apply now) »

Intéressé(e)?

Pour plus d'informations:
Appelez GWENAELLE HEBETTE
au numéro suivant: 0494 244897


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Senior Quality Engineer

Michael Page Belgium

Beerse, Antwerp
3 days ago
Beerse, Antwerp
3 days ago

Voor een speler gekend voor zijn kwaliteitsvolle producten binnen de voedingssector, zijn we vandaag opzoek naar een Quality Engineer - Future Leader dat wil meebouwen aan de toekomst van een succesvol voedingsbedrijf.
Bedrijfsomschrijving
Onze opdrachtgever is een groeiende en gerenommeerde multinational, actief in de productie van voeding.
Je kan hun producten overal ter wereld in de winkelrekken terugvinden. De sfeer binnen het bedrijf is pragmatisch en informeel, gecombineerd met een sterke gedrevenheid om dagelijks een kwalitatief, veilig en innovatief product op te leveren.
Omschrijving
  • Als Quality Engineer ben je verantwoordelijk voor klachtenbehandeling, externe audits, kwaliteit en veiligheid.
  • Je bent verantwoordelijk voor het aanbrengen van verbeteringen met een focus op continuous improvement.
  • Je werkt in een Quality Assurance team van zes en fungeert voornamelijk als rechterhand van de Food safety & Quality Manager voor de interne projecten en dagdagelijkse issues.
  • Je rapporteert aan de Food safety & Quality Manager.

Profiel van kandidaat
  • Je behaalde een relevant Masterdiploma.
  • Je hebt een relevante werkervaring in een soortgelijke omgeving.
  • Je hebt een sterke teamgeest en durft verantwoordelijkheid nemen.
  • Je werkt gestructureerd en draagt kwaliteit en voedselveiligheid hoog in het vaandel.
  • Je beschikt over de nodige affiniteit met HACCP, IFS, BRC.
  • Je spreekt Nederlands en Engels.
  • Je bent ambitieus om mee met het bedrijf te groeien.

Aanbod
Je komt terecht in een dynamische organisatie die ruimte biedt voor doorgroeimogelijkheden.
Een competitief salarispakket, aangevuld met extralegale voordelen. 4/5e is een mogelijkheid.
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IT Product / Platform Manager (Data & Analytics) in Aartselaar

People 4 Projects bvba

Aartselaar, Antwerp
2 days ago
Aartselaar, Antwerp
2 days ago

P4P is looking for a IT Product / Platform Manager (Data & Analytics) in Aartselaar.

JOB DESCRIPTION:

As a IT Product / Platform Manager (Data & Analytics), you
  • lead the design & implementation of the Intelligence Hub Platform
  • take care of the onboarding and coordination of new initiatives and projects on the platform
  • act as a single point of contact towards business and IT stakeholders
  • are responsible for managing the data platform roadmap and priorities
  • prepare budgets and stay in control of all platform related costs
  • are responsible for the implementation of governance process and quality assurance processes on the platform
  • actively drive change management by evangelizing, communicating and organizing training inside the organization.

PROFILE:

  • University master’s degree in computer science, engineering or equal through experience
  • Minimum 5 years’ experience as (IT) product/platform manager in enterprise environments
  • Excellent knowledge of English

OFFER:

  • A permanent contract of indefinite duration
  • An exciting and challenging job at an international company where you get the support
  • Training / Education opportunities
  • Attractive salary package

CONTACT:

  • Peter Weyns, 

    jasper.sneyders@p4p.be

  • Mobile: +32491869950

Location: Aartselaar
Trefwoorden: IT Product / Platform Manager Data & Analytics, Azure Cloud, SAP, Master Computer Science, IT, ICT, Antwerp, Antwerpen, Aartselaar

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Food Safety Quality Specialist

Cargill

Moeskroen, Hainaut
3 days ago
Moeskroen, Hainaut
3 days ago
Food Safety Quality Specialist-MOU00814 

Description

 

Want to build a stronger, more sustainable future and cultivate your career? Join Cargill's global team of 155,000 employees who are committed to safe, responsible and sustainable ways to nourish the world. This position is in Cargill’s food ingredients and bio-industrial business, where we anticipate trends around taste, nutrition and safety to innovate and provide solutions to manufacturers, retailers and foodservice companies.  

JOB PURPOSE AND IMPACT

The Food Safety Quality Specialist II is responsible for providing specialized knowledge of specific segments of our quality systems and/or plant processes such as food safety and quality auditing, instrumentation, specific product line knowledge, computer systems, management and/or oversight of suppliers and other needed focus areas. You will be involved in preparation and participation of customer audits. You will work together with internal and external teams to address customer requirements and concerns, as well as collaborate on audits.

KEY ACCOUNTABILITIES

  • Conducts verification and/or maintenance of the Food Safety and Quality Systems, Hazard Analysis and Critical Control Point, Sanitation Standard Operating Procedure, prerequisite programs, manufacturing processes, plant environment, and finished product.
  • Collaborates with operations on the initiation of corrective action and preventative measures when necessary.
  • Ensures adherence to corporate, regulatory, customer and facility food safety and quality requirements and completion of corrections and corrective actions.
  • Leads food safety focused audits (Corporate Food Safety, Food Safety System Certification 22000, customer, regulatory).
  • Acts as Food Safety Team leader by coordinating and leading Food Safety Team and overseeing the food safety management system and management review.
  • Manages food/feed safety management system compliance to appropriate government regulations.
  • Investigates and follow up on food safety incidents that occur in the plant to ensure they are reported and that corrective action and permanent corrections are taken.
  • Independently solve moderately complex issues with minimal supervision, while escalating more complex issues to appropriate staff.
  • Other duties as assigned

Qualifications

 

MINIMUM QUALIFICATIONS

  • Bachelor’s degree in a related field or equivalent experience
  • Fluent in English
  • Strong computer skills and Microsoft Office experience.
  • Experience with the Food Safety System Certification 22000
  • Experience working with SAP or similar
  • Knowledge of food/feed safety industry practices and standards.
  • Minimum two years of work experience in food and/or feed industry
  • Minimum of two years of related work experience

OUR OFFER
In return for your expertise and commitment, we will provide a fast paced stimulating international environment, which will stretch your abilities and channel your talents. We also offer competitive salary and benefits combined with outstanding career development opportunities in one of the largest and most solid private companies in the world.
Interested? Then make sure to send us your CV and cover letter in English today.
Follow us on LinkedIn: https://www.linkedin.com/company/cargill 

Cargill is committed to being an inclusive employer. Click here to find out more  https://careers.cargill.com/diversity/

Job

 Quality Assurance/Food Safety

Primary Location

 Belgium-WHT-Mouscron
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QA Engineer

MyNextCompany

Braine-l'Alleud, Walloon-Brabant
1 day ago
Braine-l'Alleud, Walloon-Brabant
1 day ago

We are currently looking for a Quality Assurance Engineer for a one year contract.
Mission :
You will participate in the creation and execution of functional test cases. You will be responsible for testing the newly added functionalities and validate the test results against the functional requirements as well as continuously and systematically checking for regression. As a member of the Quality Assurance team your work lies to a great extent in the acceptance testing domain. Target is to iron out any bug and improve the stability, reliability and functionality of the finished product with all its dependencies and links. For this job you work closely with the Quality Assurance Team, Project Team and Business Specialists.
Responsibilities :
  • Creation, execution and maintenance of manual test cases
  • Reporting of the defects and clearly communicating the issues
  • Raising any risks that they foresee in the validation or verification processes on time
  • Identify gaps in the functional requirement documents and ensure documentation is on par with functional requirements
  • Become a Subject Matter Expert in the product you are testing
  • Keep a critical eye on the product and come up with suggestions as a user even if it's not mentioned in the requirements
  • Work efficiently in lean agile teams
  • Be comfortable in working in short time boxed sprints, pair programming, daily stand-ups, test-driven development.

Requirements
  • At least two years of experience in structured testing of software
  • Experience in requirement analysis
  • Dutch/French + English


Technical Skills
  • Knowledge of structured testing methodologies, testing techniques, testing strategies, test tools and methodologies
  • Ability to compose test documentation (FTT trees, test procedures, test cases, checklists, etc.) and executing test cases and test procedures
  • Ability to do acceptance testing
  • Has relevant IT knowledge ; where knowledge of JIRA is a plus
  • Ability to write reports and to communicate test results

Personal Skills/Attitude
  • Flexibility
  • Stress resistant
  • Solution focused
  • Quality driven, "testing" attitude
  • Initiative & Accuracy
  • Good oral communication skills and excellent written communication skills
  • Diplomatic
  • Thoroughness and attention to details
  • Commitment to excellence
  • Ability to work independently, self-organized
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Salesforce Solution Architect

Charles River Laboratories

Brussels
21 days ago
Brussels
21 days ago
Salesforce Solution Architect
Req ID #: 87032
Location:
Wilmington, MA, US, 01887Budapest, HUWarsaw, PL, 00-124Sant Cugat del Vallès, B, ES, 08174MADRID, M, ES, 28029Brussels, Brussels-Capital Region, BE, 1030MILANO, Milan, IT, 20122Port Seton, GB, EH32 0TDTranent, GB, EH33 2NEParis, FRNorwich, CT, US, 06360Hatfield, GB, AL10 9SNHarlow, GB, CM19 5TRDublin, IE, D09Cologne, NW, DE, 51105Amsterdam, NL, 1077 ZXUSCambridge, GB, CB23 6DP
At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.
Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.
As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.
Job Summary
The Principal Solution Architect is responsible for collaborating with technology and business stakeholders to develop a scalable SalesForce technical architecture vision and strategy that enables business strategy. Partner with the business and IT leaders to ensure the architecture roadmap continually aligns with business objectives. Working closely with other IT service areas, deliver solutions that are efficient, high quality and at the best possible cost. Through excellence in delivery, help to achieve and maintain a high level of customer satisfaction.
Job Responsibilities
• Provide technical thought leadership for SalesForce platform • Ensure adherence to CRL standards and compliance with regulatory bodies are maintained (FDA, ISO, PCI, SOX, HIPPA, US, EU).• Develop SalesForce platform architecture vision and strategy that include technical roadmaps.• Design and ensure salesforce platform environment is scalable.• Identify the best solution to solve stated business problems and deliver solution options that satisfy business requirements; Including identification, analysis, selection and high-level design.• Create solution blueprints by consulting with the Customer and key IT Stakeholders.• Drive vendor selection by working with procurement and project team; Run proof of concepts as necessary.• Participate in resolving cross-functional and cross-system design issues.• Conduct requirement gathering workshops and fit gap analysis.• Assist in creating architecture standards, related processes and templates and an EA practice in CRL.• Stay current on latest technology advances particularly with SalesForce• Participate in continuous improvement of the Architecture practice.• Collaborate with peers across IT organization and business units to ensure hand-offs are well understood.• Adhere to pertinent regulatory requirements and to company policies, practices and procedures.• Perform all other related duties as assigned.
• Contribute to building a high-performance team.
Job Qualifications
Education: Bachelor’s degree (B.A./B.S.) or equivalent in Computer Science, Engineering, or a related discipline.Experience: Minimum of 10 years working as a SalesForce Solution Architect.Have experience with multiple salesforce implementationsSolid understanding and demonstrated ability for the following:• Demonstrated leadership and influencing skills at all levels• Effectively communicate and make technical information consumable to large, multi-national audiences• Have proven emotional intelligence (EQ) and relationship building skills• Be able to conceptualize and develop impartial alternative solution approaches, articulating the benefits and tradeoffs of each.• Customer consulting skills• Experience building Technology roadmaps• Experience working in an Agile/ product and platform centric operating model
About Corporate Functions
The Corporate Functions provide operational support across Charles River in areas such as Human Resources, Finance, IT, Legal, Sales, Quality Assurance, Marketing, and Corporate Development. They partner with their colleagues across the company to develop and drive strategies and to set global standards. The functions are essential to providing a bridge between strategic vision and operational readiness, to ensure ongoing functional innovation and capability improvement.
About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 17,000 employees within 90 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of ~85% of the drugs approved by the FDA in 2019.
Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit www.criver.com.
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Senior Advisor Scientific and Regulatory Affairs Starches and Sweeteners

Cargill

Peutie, Flemish Brabant
25 days ago
Peutie, Flemish Brabant
25 days ago
Senior Advisor Scientific and Regulatory Affairs Starches and Sweeteners-REG02499 

Description

 
Want to build a stronger, more sustainable future and cultivate your career? Join Cargill's global team of 155,000 employees who use new technologies, dynamic insights and over 155  years of experience to connect farmers with markets, customers with ingredients, and people and animals with the food they need to thrive.
 
The primary location is Vilvoorde, Belgium. Open for candidates based in remote locations in Europe.
 
JOB PURPOSE AND IMPACT
The Senior Advisor Scientific and Regulatory Affairs Starches and Sweeteners will identify, set and drive regulatory activities and strategic direction for growth and freedom to operate for starches and sweeteners product group throughout Europe. We seek a leader who will work closely with food safety quality and regulatory operations, governmental relations , research and development and  partner with a broad set of key stakeholders, internally and externally, to define and enable compliance systems and processes, develop and cultivate strong relationships and knowledge, and enable commercial teams to establish and achieve business objectives and growth strategies.

KEY ACCOUNTABILITIES
  • Be the main regulatory and scientific affairs contact across functions for starches and sweeteners product group including product lines, key customers and commercial leaders.
  • Provide strategy and guidance, and coordinate the regulatory affairs initiatives within starches and sweeteners product group in the region to define the regulatory compliance for existing products, products destine for export.
  • Provide thought leadership in regulatory and scientific affairs area in the region including midterm and long term emerging issues.
  • Partner with food safety quality and regulatory and research and development colleagues to assess and implement programs and processes that enable regulatory compliance and innovation and priorities.
  • Monitor, understand, anticipate, and interpret regulatory changes. Share and train related functions to improve partnering and effectiveness.
  • Develop and coordinate regulatory positions, requirements, and processes by working with commercial teams and functional units, governmental relations, key customers, and external regulatory agencies.
  • Develop strong coordination and connections globally within our product groups and regionally across product groups to leverage synergies and ensure continuous development and enable capacity building for executing regulatory compliance and innovation.
  • Provide expert thought leadership in your field and work with limited direction, using additional research and interpretation to identify issues or problems. You may provide direction to supporting team members and be a strategic contributor.
  • Other duties as assigned

Qualifications

 
MINIMUM QUALIFICATIONS
  • Bachelor’s degree in science or law; or Regulatory Safety experience with a majority of time in a food manufacturing companies
  • Advanced knowledge of food laws and regulations relevant to starches and sweeteners product group
  • Minimum of six years of related work experience
  • Fluent in English speaking and writing
 
PREFERRED QUALIFICATIONS
  • Master's degree in science or law
  • 10 years of professional regulatory experience with most of the time in food/feed/pharma companies
  • Strong relationship with government agencies in the region
  • Active participation in key Trade Association(s) in the region
  • Advanced knowledge of food laws & regulations in EU & starches and sweeteners Subject matter expert
  • Advanced management and regulatory processes improvement skills – delivering processes that are aligned, effective, and optimize Cargill resources
  • Advanced communication and interpersonal skills
  • Advanced project management skills
  • Advanced training / meeting management
  • Advanced scientific knowledge - applying scientific knowledge in quality and food safety, and to provide input during new product development

 

OUR OFFER
In return for your expertise and commitment, we will provide a fast paced stimulating international environment, which will stretch your abilities and channel your talents. We also offer competitive salary and benefits combined with outstanding career development opportunities in one of the largest and most solid private companies in the world.
Interested? Then make sure to send us your CV and cover letter in English today.
Follow us on LinkedIn:
https://www.linkedin.com/company/cargill
Cargill is committed to being an inclusive employer. Click here to find out more  https://careers.cargill.com/diversity/ 

Job

 Quality Assurance/Food Safety

Primary Location

 Belgium-BRU-Vilvoorde

Other Locations

 Spain, Germany, France, Netherlands
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QA Specialist - Mechelen,BE

Galapagos

Mechelen, Antwerp
14 days ago
Mechelen, Antwerp
14 days ago

Pleased to meet you, we are Galapagos, a dynamic fast growing Biotech company with offices in Europe in Belgium (Mechelen), France (Romainville & Paris), the Netherlands (Leiden), Switzerland (Basel), Italy (Milano), Spain (Madrid), the UK (London), Germany (München), and in the US (Boston).

We are in the business of changing lives. In our quest to discover and develop life-improving medicines we go where no one has ever gone before. In every challenge we face, we see new opportunities. We want to challenge the impossible. We need thought leaders and rapid thinkers, entrepreneurs in spirit and status quo-fighters. Collaborative innovators and perseverant idealists. We need the best-in-class. In other words, we need you.


We are looking for a QA Specialist - Mechelen, BE


Scope of the role:

You will mainly collaborate with the Quality Assurance Lead and will conduct the delegated QA lead activities, providing the necessary support in QA dedicated project.


Principal Accountabilities:

  • Coordinate the delegated audit activities as per current Master Audit Plan under supervision of QA lead
  • Participate in the auditor selection and manage contractual agreements included related documents (e.g. review of proposals, initiating SoW creation)
  • Support maintenance of qualified providers list
  • Coordinate of delegated audit activities and CAPA formulation, follow up on CAPA implementation until audit closure
  • Generates reports to follow up and to ensure oversight on audit activities and CAPAs status
  • Process quality assessment in Audit Management System, managing contract agreements in case of external quality assessments and follow up on related CAPAs, when applicable
  • Continuous improvements activities handling of AMS system in cooperation with IS system owner
  • Defining the reporting mechanism in the Audit Management System to allow proper/meaningful reporting to the respective stakeholders being business & senior management
  • Support coordination and preparation of regulatory agency inspections and other assessments by external bodies
  • Handling and follow up of Product Quality Complaints (PQC)
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Director, Cloud and End User Technology

Charles River Laboratories

Brussels
21 days ago
Brussels
21 days ago
Director, Cloud and End User Technology
Req ID #: 83662
Location:
Wilmington, MA, US, 01887Sant Cugat del Vallès, B, ES, 08174Reno, NV, US, 89511Spencerville, OH, US, 45887Copenhagen, DKPort Seton, GB, EH32 0TDCambridge, GB, CB23 6DPBudapest, HUHorsham, PA, US, 19044Saffron Walden, GB, CB10 1XLCharleston, SC, US, 29407Harlow, GB, CM19 5TRRaleigh, NC, US, 27610Brussels, Brussels-Capital Region, BE, 1030Dublin, IE, D09Tranent, GB, EH33 2NEAmsterdam, NL, 1077 ZXMADRID, M, ES, 28029Paris, FRMattawan, MI, US, 49071
At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.
Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.
As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.
Job Summary
For nearly 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and wellbeing of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
The CRL IT organization is looking for an energetic professional to manage, lead and own the hybrid cloud and end user computing infrastructure (product) within the Global Infrastructure Services team. As a manager; responsible for building, coaching and developing a high performing engineering team. As a product owner; responsible for hybrid cloud and end user computing infrastructure services. The Product Manager/Owner will lead and own the delivery of effective end to end hybrid cloud and end user infrastructure technology solutions.
Through excellence in delivery, he/she will help to achieve and maintain a high level of employee engagement, customer satisfaction and team productivity.
Role Accountabilities:• Accountable for owning hybrid cloud and end user infrastructure end to end including management, costing, and continuous improvement opportunities.• Accountable for leading a high performing team that delivers consumable, standardized hybrid cloud and end user infrastructure services and solutions (resilient, high quality, highly automated and up-to-date)• Accountable for collaborating and consulting with other IT practices to support technical solution development and deployment• Accountable for working with external strategic partners to develop and deliver technical solutions
Essential Duties and Responsibilities: • Own the infrastructure product end to end.• Work with the infrastructure integrator to ensure that designs and blueprints incorporate best practices.• Approve all designs and blueprints that are to be incorporated in the owner’s product.• Ensure that the infrastructure product team is functional.• Manage the infrastructure product at the service level.• Deliver and manage value-added services based on an understanding of cost, risk, compliance and business value, while making informed decisions based on continuous measurement.• Identify, prioritize and implement product improvement opportunities.• Manage policies/design versions and track issues.• Coordinate infrastructure product release.• Responsible for overall infrastructure product definition.• Responsible for infrastructure product costing and financial models for infrastructure product offerings.
Essential Duties & Responsibilities
Required Qualifications:• Bachelor’s degree (B.A./B.S.) or equivalent in computer science, engineering, or related discipline; an equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education listed above.• Minimum of ten (10) years related experience in IT infrastructure, including cloud infrastructure design and implementation.• Minimum five (5) years of experience in IT management role.• Experience and understanding of Agile Methodologies • In depth knowledge of hybrid cloud infrastructure design and implementation • Strong knowledge and understanding of current Cloud Computing technologies such as Azure and AWS and cluster management tools like Kubernetes• Strong knowledge of Infrastructure as Code tooling• Strong communication skills for large, multi-national audiences. • Strong cross-functional leadership and collaboration skills. • Utility player – broad understanding of tools and technologies• Flexibility and willingness to learn new toolsets and solutions• Ability and willingness to coach and mentor engineers • Business acumen –understanding of customer value • Operational Performance – Understanding of and/or experience with Theory of Constraints (TOC).
About Corporate Functions The Corporate Functions provide operational support across Charles River in areas such as Human Resources, Finance, IT, Legal, Sales, Quality Assurance, Marketing, and Corporate Development. They partner with their colleagues across the company to develop and drive strategies and to set global standards. The functions are essential to providing a bridge between strategic vision and operational readiness, to ensure ongoing functional innovation and capability improvement.
About Charles RiverCharles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 17,000 employees within 90 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of ~85% of the drugs approved by the FDA in 2019.
Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit www.criver.com.
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Application Architect (17011, L4)

Serco European Agencies

Brussels, Brussels
1 day ago
Brussels, Brussels
1 day ago
Job Description

Excellent Salary 

Corporate Benefits Package 

Relocation Assistance (if applicable)

Further information available from the Serco Europe Recruitment Team

Job Introduction

At Serco not only is the nature of the work we do important, everyone has an important role to play, from caring for vulnerable people to managing complex public services.
We are a team of 50,000 people responsible for delivering essential public services around the world, we are innovators,committed to redesigning and improving public services for the benefit of everyone.

Serco and Proud - Make a difference every day.

We currently have an exciting opportunity for an Application Architect, in an International Organisation, based in Brussels.

 

Main Responsibilities
  • Analysis, design and implementation of components and modules of DGT’s workflow applicationsin JAVA code.
  • Elaboration of integration scenarios of different information systems in a SOA.
  • Adaptations to existing modules, development and re-factoring of Java code.
  • Analysis of production issues and elaboration of specific solutions (Bug fixing).
  • Technical analysis of change requests.
  • Provision of studies, assessments, technical guidance and evaluations.
  • Assistance in testing, evaluation and reporting.
  • Elaboration of written documentation.
  • Quality assurance of new modules/developments.
  • Prototyping.

 

Successful Candidate
  • Successful studies in an IT area with master’s level or 5 years of higher education. Remark: Where the minimum number of years of education is not fulfilled, 2 years of professional experience will be considered as equivalent for 1 year of study.
  • Minimum 11 years of practical experience as an IT professional.
  • Minimum 6 years of practical experience of Java Enterprise/JEE and relevant development frameworks, such as Vaadin 6, Vaadin 8, JSF, Java UI (AWT/Swing).
  • Experience with Oracle Weblogic server, web technologies, web services, javascript, XML, Oracle databases and PL/SQL.
  • Proven experience in architecture and design of mission-critical IT systems and professional Software Engineering in general.
  • Knowledge of Service Oriented Architectures(SOA).
  • Experience in the domain of language and translation applications would be an asset.
  • Knowledge of the Commission’s IT environment would be an asset.
  • Capability to work in a structured way and to communicate with users, other developers and support staff.
  • Strong analytical skills. Ability to work under pressure and to deliver to tight deadlines.
  • Ability to participate in multi-lingual meetings, good communication skills.
  • Fluent in English.

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Important

Any offer of employment is contingent upon you providing documents to verify your identity and employment eligibility, as required by law.

Applicants are reminded that they will be requested to produce such documentation during the recruitment process.

Please contact a member of the recruitment team if you require further details of acceptable types of documentation required for verification of identity and work authorization. 

Data Protection:

When creating a profile on the Serco Career Centre you agreed to the Data Protection policy, a copy is available upon request.

You may submit a written request revoking your consent to this agreement at any time.

Job Type

Full Time

Posted

11 days ago

Description

Pour soutenir son développement, EyeD Pharma recherche un Medical Device Specialist.

Fonction

  • Vous êtes en charge du développement des dispositifs médicaux
  • Vous fournissez une expertise technique dans les domaines suivants :
    1. Définition des Design Inputs
    2. Planification et exécution des études nécessaires à l’établissement des Design Outputs
    3. Mise en place de la stratégie de vérification et de validation et suivi de son exécution
    4. Mise en place et exécution de la stratégie de gestion des risques liés aux produits
  • Vous êtes familier avec les outils de Quality-by-Design et les appliquer adéquatement
  • Vous coordonnez et supervisez les activités réalisées par les sous-traitants
  • Vous êtes responsable de la constitution de la documentation technique
  • Vous garantissez la conformité aux procédures d'exploitation standard et aux exigences réglementaires pour les produits combinés selon les normes européennes et américaines
  • Vous collaborez de manière constructive et bienveillante avec chaque membre du personnel impliqués dans le projet (contrôle qualité, assurance qualité, CMC, production, RA, etc)
  • Vous réalisez des expériences appropriées pour résoudre les problèmes techniques et réduire les risques
  • Vous gérez de manière efficace et cohérente vos projets

Mots clés : medical device, ophthalmology, development, pharmaceutical, ocular pathologies, research scientist, quality, drug product, chemistry, chemical, life sciences, sciences appliqués, innovation, technical documentation, MDR, GSPR, design control, dispositifs médicaux, research scientist, ISO14971, ISO13485, Risk management, Verification and validation (V&V)

Profil

  • Vous avez un minimum de 3 ans d'expérience dans l'industrie pharmaceutique et plus précisément dans les dispositifs médicaux
  • Vous avez un diplôme universitaire en sciences appliquées, de préférence en génie chimique ou biomédical, en sciences pharmaceutiques ou en chimie des polymères
  • Vous avez une expérience dans le développement de dispositifs médicaux
  • Vous avez une expérience en matière de gestion des risques liés à la qualité (ISO 14971 ; ICH Q9)
  • Une expérience dans le domaine des systèmes d'administration de médicaments basés sur la technologie des polymères est un plus
  • Des compétences avérées en matière de gestion de projets sont un atout.
  • Vous avez de très bonnes connaissances des exigences en termes de réglementation de développement des dispositifs médicaux (MDR, ISO 13485)
  • Vous parlez couramment l'anglais et le français
  • Vous avez une excellente communication écrite et oral dans les deux langues et vous échangez avec beaucoup de bienveillance avec vos collègues
  • Vous faites preuve d’esprit d’équipe, d’une attitude proactive et vous êtes disposé(e) à travailler dans un environnement « start-up »

Offre

EyeD Pharma vous propose un CDI, à temps plein, dans un environnement de travail convivial avec des projets passionnants et innovants.

« Profile Group gère cette mission en exclusivité. Tout candidat intéressé est donc invité à postuler exclusivement via cette annonce (apply now) »

Intéressé(e)?

Pour plus d'informations:
Appelez GWENAELLE HEBETTE
au numéro suivant: 0494 244897