41 jobs voor quality inspection manager gevonden

Proactively support the activities of Development Quality Lead for relevant laboratory/manufacturing quality systems (deviation close out / change management/ complaints/ quality improvement).Ensure Development Quality Management System directly support Technical Operations and development partner goals and objectives.

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

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

Monitor machine operations during production runs and troubleshoot any issues that arise.Testing and inspection of manufactured workpieces on determined specifications (dimensions, surface qualities,), this includes using a CMM.

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.

For our client you will work in the 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 out client).
• 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.

* 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.

Grinding and deburring aluminum profiles according to technical drawings.Using visual inspection and precise measuring instruments to ensure the quality of your grinding work.

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..

Kwaliteitsborging: beheren en up to date houden van HACCP plannen, coördineren van audits en optimaliseren van interne processen Productcontroles: grondstoffen en eindproducten inspecteren om de hoogste kwaliteit te garanderen Preventie & training: preventieplannen opstellen en het team opleiden om kwaliteit en voedselveiligheid naar een hoger niveau te tillen Klachtenbeheer: analyseren en oplossen van kwaliteitsproblemen, zodat onze klanten steeds tevreden zijn

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.

Kwaliteitsborging: beheren en up to date houden van HACCP plannen, coördineren van audits en optimaliseren van interne processen Productcontroles: grondstoffen en eindproducten inspecteren om de hoogste kwaliteit te garanderen Preventie & training: preventieplannen opstellen en het team opleiden om kwaliteit en voedselveiligheid naar een hoger niveau te tillen Klachtenbeheer: analyseren en oplossen van kwaliteitsproblemen, zodat onze klanten steeds tevreden zijn

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.

Technical Project Manager Nuclear (F/M/X), you’ll play a key role in supporting our future business and delivering impactful results..Your Responsibilities:.

As QC analyst you are responsible for controlling all quality aspects for the production of dental materials.The production exists out of following sections: investments, stones, Glass Ionomer, composite, Assembly and scanner department.

You identify mechanical and electrical issues and perform repairs or maintenance on vans, trucks, and buses.Ensure top quality: Fix it right first time, we trust you to inspect our vehicles diligently before return and pre delivery and to work with the highest quality standards?

Our main activities are inspection, control activities, certification, training and consultancy.In order to best guarantee our service and our relationships with customers, Vinçotte operates from various locations in Belgium.

We employ over 300 highly skilled, passionate and enthusiastic employees.Our Operations department is currently looking for an OPERATIONS SUPERVISOR:The Supervisor 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.Your role:You organize and supervise the work within your team (technical performers: Jet Engine Mechanics, Inspectors, and Repair Operators) alternating between two shifts;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..

Designing pressure equipment.Developing thermal solutions by analyzing system behavior.

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.

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