42 jobs voor quality inspection manager gevonden

Plans, organizes, coordinates and supervises Field QA/QC Inspection Group at the jobsite and at off site prefab sites if applicable..Maintains interface with construction supervision, client, government representatives and Notified Body's on matters concerning quality..

Jobomschrijving.Drive continuous improvement and lean initiatives across quality control, production, and warehouse departments..

.Quality Control:..Conduct rigorous quality control inspections of mechanical installations..

Key Responsibilities:

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• Perform quality checks and inspections on products and processes
• Ensure compliance with Good Manufacturing Practices (GMP) and company standards
• Maintain and improve the Quality Management System (QMS), ensuring that all quality procedures and policies are up to date
• Investigate, document, and resolve product Deviations, ensuring timely implementation of corrective actions
• Initiate and manage CAPA processes to address non-conformances, ensuring long-term solutions are implemented
• Conduct internal audits and prepare reports on quality performance
• Collaborate with cross-functional teams to continuously improve quality processes
• Ensure accurate and thorough documentation of all quality control activities

Leidinggeven aan een team van quality engineers, incoming inspection operators en Q auditors . ..Actief bijdragen aan audits, risico evaluaties en veiligheidsrondgangen .

BRC, ACS, GMP+/FSA), external sustainability certification audits (incl.BIO/NOP, Fairtrade, Kosher, Halal, UTZ, Rainforest Alliance), inspections of authorities, customer audits and Puratos Group audits (e.g.

Our client is a manufacturer for automotive parts.

You will work in the VCST E-drives prototyping and testing area, where you will support with the administrative work related to the quality assurance, prototyping and validation of new generation Electronic Drive Units (EDUs).

The following tasks will be assigned to you:

• You will support with the incoming goods inspection and quality control: perform visual inspection; manual and CMM measurements on parts and provide the measurement reports to the design team (training on this topic will be foreseen by VCST).
• Pick prototype parts according to a pick list to compose a new powertrain.
• Prepare the build reports for new transmissions and assure that parts can be traced.
• Requesting quotes for parts and tooling, placing orders in the system and follow up on order approval and deliveries.
• Managing the warehouse and stock of the prototyping area.
• Writing of test reports and providing support with a variety of administrative tasks.

BRC, ACS, GMP+/FSA), external sustainability certification audits (incl.BIO/NOP, Fairtrade, Kosher, Halal, UTZ, Rainforest Alliance), inspections of authorities, customer audits and Puratos Group audits (e.g.

You are responsible for operational technical excellence, including the application of best practices, and assesses the skills of Technical Performers as part of their training.Safran Aircraft Engine Services Brussels is a subsidiary of Safran Aircraft Engines, based at Brussels Airport (Zaventem, Belgium), specialized in the inspection, maintenance and repair (MRO) of the advanced LEAP jet engines that power the latest generation of the Airbus A320NEO & Boeing B737MAX narrow body families.The company is a key player in the integrated CFM international MRO network.

Taking samples from the water purification system.Reporting to the quality manager.You control various processes (from blanching and the mixing department) and the final inspection.Completing the necessary quality documents.

* Being able to perform basic operations in different solutions (My Organization, My Location Manager, My Product Manager, My Coupon Manager, etc.).
* Preparing quotes, orders, and invoices when necessary.
* Managing the customer base in CRM.
* Maintaining data, such as contact persons, billing information, turnover, etc., and/or actively encouraging companies to do so.
* Understanding the literal and technical link between the CRM and the solutions that the organization offers.
* Providing the correct settings so that every company has the necessary access (or not).
* Signaling, identifying, and providing feedback to customer needs internally.This includes being able to identify prospects who are not yet customers.
* Sharing acquired knowledge with other employees within the organization and proactively reporting to the team lead.

* Ensuring a quality result of the checks carried out on the products based on the 4-eyes principle.
* Ensuring sufficient feedback to those carrying out the 1st inspection.
* Communicating the gaps to the project owner and team lead to increase quality.
* Being critical and analyzing the available documentation, keeping it up to date, and finding customer-oriented solutions.

Our client, situated in Genk, is looking for an engineer Vision Expert. 

They have launched an ambitious programme to increase the level of quality in its European facilities.Improving product control is a key element of this programme, particularly by enhancing the use of Automatic Surface Inspection Systems (ASIS) in our cold mill in Genk. 

Your main accountabilities: 

• Increase the usage of the current equipments
• Enhance defect recognition and classification, with the support of local Quality Control and/or by using innovative learning techniques
• Develop automatic coil grading
• Train different users (control, allocation, …)
• Upgrade current equipment
• In collaboration with the suppliers, develop new functionalities that meet the needs of the users: new type of defect, new display, …
• Develop classification algorithm, in cooperation with suppliers and by using innovative learning techniques
• Support the installation of new devices
• Define the specifications
• Meet potential suppliers
• Coordinate the installation, in relationship with maintenance and engineering
• Develop classification algorithm, in cooperation with suppliers and by using innovative learning techniques
• Train the users
• Apply vision on existing cameras
• Extract and process streaming video / images from existing and / or new matrix or line scan cameras using open source software
• Integration in IT architecture
• Develops knowledge of ASIS data usage (link with visual inspection, link with supply chain systems, link with data platform project, link with data science studies) and integration of ASIS in IT architecture
  

Collaborating with different departments, including quality and operations, to support ongoing production and lab activities..Completing necessary documentation in line with GMP (Good Manufacturing Practices) and ensuring all procedures adhere to quality standards..

Using visual inspection and precise measuring instruments to ensure the quality of your grinding work.Using our ERP system (Navision) to manage orders.Performing first line maintenance on equipment.

Ensuring compliance with regulatory requirements and standards in all pharmaceutical procedures (production and distribution processes)..Contributing to the development of quality control procedures and policies..

.Kwalitatieve Case management.Analyseer en communiceer alle gegevens met betrekking tot internal rejects, coördineer oplossingen..Analyseer en communiceer alle gegevens met betrekking tot kwaliteitsprestaties van de klant.

As Warehouse Support you are responsible for the optimal flow of (pharmaceutical) goods in the warehouse.Important: this is not a regular warehouse, but a cleanroom environment that requires strict protocols.

Bedrijfsomschrijving

Our client is one of the leading companies in the pharmaceutical industry.
This organization is at the forefront of developing cutting-edge cell therapies that have the potential to transform lives.The position is based at their site in the Ghent area, where they are launching new and innovative facilities.

Omschrijving

• Receiving, inspecting, and managing inventory, including biohazard products, in a controlled environment.
• Ensuring the safe handling of cryo-frozen materials using specialized equipment and PPE.
• Collaborating with different departments, including quality and operations, to support ongoing production and lab activities.
• Completing necessary documentation in line with GMP (Good Manufacturing Practices) and ensuring all procedures adhere to quality standards.
• Working with SAP systems for inventory management and contributing to the development of standard operating procedures.

We employ over 300 highly skilled, passionate and enthusiastic employees.Your role:You prepare and submit certification files to national authorities and certification bodies.You analyze quality standards, norms, customer specifications, contracts and aviation regulations and adapt internal procedures or manuals, or draft new procedures.You organize and supervise external audits of customers, authorities and certification organisations and handle the findings.You are part of the validation process of suppliers and subcontractors and monitor the process regarding the quality of the delivered products and services.You support the owners of the processes in dealing with quality deviations/findings, using quality basic techniques.You propose actions to improve the efficiency of the business processes.You prepare presentations and provide training to colleagues on quality topics.You participate in multidisciplinary projects.You conduct internal quality audits, provide reporting of findings and follow up on corrective actions.You assist in the statistical analysis of data and its reporting.

Upon request of clients, be responsible for batch release certification of (investigational) medicinal products.

Implement MES production, quality, and customer standards..Document deviations and carry out corrective measures..Develop and implement measures for preventative quality assurance.

The TMF Records Specialist is a member of the core trial team and is responsible to provide operational expertise to the core trial team, oversees the implementation of the (Trial Master File) TMF strategy for the trial and supports the core trial team in all aspects of TMF management and in inspections or audits.

The TMF Records Specialist provides and maintains oversight and guidance related to TMF activities throughout the course of the trial, to safeguard the protection of the trial subject, reliability of the trial results, compliance with study protocol, ICH-GCP and applicable regulations and ensure inspection readiness at all times.

The TMF Records Specialist closely collaborates with the core trial team to create, implement and maintain the list of trial specific expected records.This includes the identification of all relevant trial level records required to reconstruct the trial, independent of owner or system hosting the record.

In this role you are responsible for the planning, tracking, formal QC and filing of all TMF trial level records according to internal and external standards and also to initiate the close out of the TMF.Besides you will share the status to the core trial team on the completeness, quality and timeliness of the TMF during the entire life cycle of the trial.

Conduct regular performance reviews, set clear expectations, and facilitate professional development opportunities for team members .client relationship management:.quality assurance and control:.. Team leadership and management:..

We employ over 300 highly skilled, passionate and enthusiastic employees.Our Operations department is currently looking for an OPERATIONS TEAM LEADER: The Operations Team Leader ensures the proper preparation and follow up of their team's activities in accordance with the applicable company standards.They manage the distribution of work to achieve the weekly objectives and any priorities communicated by the Operations Shift Manager and/or the Operations Manager.You organize and supervise the work within your team (technical performers: Jet Engine Mechanics, Inspectors, and Repair Operators) alternating between two shifts (6AM 2PM, 2PM 10PM);You provide practical support to the team on the engine or engine sub assembly using equipment specific to the field of activity;You participate in on the job team meetings, ensuring problem resolution and continuous improvement of the production process;You regularly communicate with the Operations Shift Manager about important matters related to the daily functioning of your team and ensure handover to guarantee the smooth continuity of activities;You ensure and verify that safety, hygiene, quality rules and work regulations are properly applied within the company;You continuously evaluate the performance and attitude of your team members and provide guidance for continuous improvement;You regularly and effectively communicate with support services, management, Safran Group, instructors, and potential subcontractors.

.Receiving biohazard products (blood bags, viral vectors,) in a controlled temperature environment..

Freezing therapeutic products.Managing equipment: inspections and maintenance.Daily aseptic and manual production processes.Executing production steps in controlled environments (grade A/B/C/D) Spiking.

Managing equipment: inspections and maintenance.Thorough cleaning and disinfection of materials.Executing production steps in controlled environments (grade A/B/C/D) Spiking.Media refreshing. .Daily aseptic and manual production processes.

For our client, we are looking for a qualified maintenance technician to join the team at OEVEL.
The company manufactures hydrogen plants.Mainly for industrial purposes.The plants are developed, designed and manufactured entirely on the company's premises.

Your tasks
- As a maintenance technician you will be responsible, together with your colleagues, for the mechanical and/or electromechanical maintenance and repair of various machines and equipment.
- You will regularly inspect machines on the floor and perform preventive maintenance.
- Detecting, reporting and resolving problems in cooperation with the facility engineer.
- Collaborate with and/or supervise co-workers, giving instructions and guidance on how to perform work.
- Striving for continuous improvement in safety, environmental protection, quality, cost and productivity.
- Equipping the workplace with the necessary safety signs, labels and signals in consultation with the safety department.
- Support the safety manager in the practical development of safety-related activities.

Capsule filling machine), but also globally used web applications, Clinical Trial Management Systems, complex Manufacturing Execution Systems, SAP systems, medical devices, etc…