16 jobs voor manufacturing consultant gevonden

Je.test de applicaties,.Ze zijn sterk aan het groeien en innoveren, daarom zijn zij op zoek naar een.functional consultant (manufacturing management).. Je bent de.liaison tussen de business en de implementatiepartner..

Manage quality systems, e.g.change control, deviations, and product investigations..

Beheer de Elastic Infrastructure en SIEM van Telco, Life Sciences tot Manufacturing & Government.

Als functioneel consultant ben je verantwoordelijk voor de.ontwikkel , plannings en productieprocessen in het applicatie landschap van DUCO..architectuur van het applicatie landschap qua functionaliteit, data en integratie..Je monitort de goeie.

Protect our customers against security threats and keep evolving with the Elastic stack.

Content is at the core of everything we do.We design, create and maintain tailor-made digital content experiences that are an answer to the individual needs of different organisations.Our technology partners support us in our mission and enable us to provide the answers to the different challenges organisations face today.

Ready to start working with proven technology and deliver state-of-the-art digital content experiences and take your career into your own hands?

Our ideal Elastic Security consultant is:

• An Elastic enthusiast with an analytical mindset.
• A positive communicator who can understand the needs of the client and communicate with the team.

Your skills include:

• ELK (Elasticsearch, Logstash, Kibana) stack
• System engineering
• Knowledge about the MITRE ATT&CK framework is a plus

We offer:

• Great team spirit - An amazing start-up spirit with all the benefits and security of a scaled company as part of the Cronos Group.
• Support to broaden your Elastic knowledge - The Elastic stack grows and evolves fast.We give you the opportunity to grow with it, get certification and obtain market visibility (if you like that).
• You matter - Opportunity to deepen your knowledge and continue on a path that suits you best.
• Diverse projects  – We have projects ranging from Telco, Life Sciences to Manufacturing & Government.

Referentiestandaarden.Continuous Manufacturing.Release.Stability (ICH, stress study, RIBPS).

As an ALTEN consultant, you will have the opportunity to be part of the following activities:Ensure the release of batches of pharmaceutical products in accordance with local and international regulations Act as the quality assurance representative to approve production activities and associated documentation Perform critical reviews of batch records, including certificates of analysis, manufacturing and control protocols, and test reports Work closely with production, quality control, and pharmaceutical development teams to ensure the quality of pharmaceutical products Ensure that facilities, equipment, processes, and procedures are in compliance with quality and safety standards Participate in incident, deviation, and change management, and conduct quality investigations Maintain a thorough knowledge of local and international regulations related to batch release and regulatory compliance

Ondersteuning bieden bij kleinere optimalisatieprojecten en taken binnen het QA Commercial Operations team.Bevorder en onderhoud sterke samenwerkingsrelaties met zakelijke en kwaliteitspartners..

Hier licht je met je kennis van procesverbetering, de duidelijke meerwaarde van een PLM systeem concreet toe en overtuig je klanten om naar 'the next level' te gaan..Je aanspreekpartners bij de klanten zijn CXO's, engineering managers en ontwerpingenieurs die de producten van morgen ontwikkelen..

Je onderhoudt kennis van Good Manufacturing Practices (GMP) en ICH Guidelines.

Communicatief, zeker naar andere afdelingen toe Kan goed omgaan met deadlines, is flexibel Analytische denker Sterk gevoel voor technologie Voorkeursachtergrond: Industrieel ingenieur, burgerlijk ingenieur, master of PhD

Speicified seeking a highly motivated Engineering Consultant to join our team.In this role, you will leverage your technical expertise and analytical skills to provide innovative solutions for our clients across various sectors.You will work closely with clients to understand their challenges, develop tailored strategies, and support the implementation of engineering projects.

Location: Antwerp/Ghent/Brussels

Key Responsibilities:

• Design, develop, and implement automated systems and controls for manufacturing processes.
• Program and configure PLCs, HMI interfaces, and SCADA systems.
• Maintain and troubleshoot existing automation systems to ensure optimal performance.
• Conduct feasibility analyses and cost estimates for automation projects.
• Develop and maintain technical documentation, including system specifications, user manuals, and training materials.

Qualifications:

• Master's degree in Automation Engineering, Electrical Engineering, or a related field.
• Bachelor's degree in Automation combined with notable experience.
• 2-3 years of experience in automation engineering or a similar role.
• Proficiency in programming languages (e.g., Python, C++, ladder logic) and automation software.
• Strong understanding of control systems, robotics, and industrial networking.
• Excellent analytical and problem-solving skills.
• Strong communication and teamwork skills.

Support the design supportive studies required.Support the introduction of new raw materials in close collaboration with process teams (supplier selection criteria at early stage, IPC/specifications definitions, shelf life definitions,.) Improve raw materials usage in collaboration with process development and clinical manufacturing.

Transfer to the manufacturing unit and troubleshooting of the commercial activities .Identify, Evaluate & Coordinate the scientific efforts supporting the development of Devices, Delivery Systems and Packaging o Promote and lead innovative approaches and design of future Patient Solutions o Support innovative technology platforms to allow a fast and agile support to all relevant company stakeholders o To maintain and develop scientific expertise through scientific literature, meetings or continuing education opportunities.

Provide a compliance expertise in validation :

• Ensure QA oversight in validation activities (IQOQ / PQ / PV…)
• Review/Approve the validation documentation regarding the GMP requirements and the Vaccines procedures
• Ensure that production practices are aligned with validation conclusion
• Attend all project meetings as QA validation representative
• Ensure timely escalation to Management of critical issues during validation
• Contribute to the deviation process providing QA oversight and approving deviation for deviations related to validation activities and/or impact of manufacturing deviations to validation activities
• Pro-actively identify potential quality and compliance risks and manage these risks through the risk register and quality plan process
• Work in autonomy with supervision/coaching
• To define the validation strategies through the change control process
• To write and implement some validation documentation (Validation Plan, Validation Summary Report, Risk Assessment, Gap Analysis , Periodic review ….)
• To ensure the correct application of the validation quality systems in the field and to define improvement plan as required
• To support the production, QA and technical service teams in the implementation of the validation activities.

New product introductions, design and packaging configuration changes, modifications to sterilization process and equipment, …).g.