67 jobs voor quality inspection manager gevonden

As a Quality Manager you'll be leading the charge towards excellence, embarking on a diverse array of tasks each day.Your mission?to oversee meticulous quality inspections and foster seamless collaboration across departments

The client is a global leader in chocolate and cocoa production, renowned for quality, innovation, and sustainability.

Your missions as a Quality Manager:

• Oversee the implementation and maintenance of quality management systems in the laboratory.
• Conduct quality control tests and inspections to ensure accuracy and reliability of results.
• Develop and update standard operating procedures (SOPs) to meet regulatory standards.
• Investigate deviations or non-conformities, identifying root causes and implementing corrective actions.
• Train laboratory staff on quality protocols, safety procedures, and best practices to uphold quality standards.

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..

As a Quality Manager you'll be leading the charge towards excellence, embarking on a diverse array of tasks each day.Your mission?to oversee meticulous quality inspections and foster seamless collaboration across departments

The client is a global leader in the food industry, renowned for quality, innovation, and sustainability.The facility is located in the South Henaut region.

Your missions as a Quality Manager:

• Oversee the implementation and maintenance of quality management systems in the laboratory.
• Conduct quality control tests and inspections to ensure accuracy and reliability of results.
• Develop and update standard operating procedures (SOPs) to meet regulatory standards.
• Investigate deviations or non-conformities, identifying root causes and implementing corrective actions.
• Train laboratory staff on quality protocols, safety procedures, and best practices to uphold quality standards.

As a Quality Manager you'll be leading the charge towards excellence, embarking on a diverse array of tasks each day.Your mission?to oversee meticulous quality inspections and foster seamless collaboration across departments

The client is a global leader in the food industry, renowned for quality, innovation, and sustainability.The facility is located in the South Henaut region.

Your missions as a Quality Manager:

• Oversee the implementation and maintenance of quality management systems in the laboratory.
• Conduct quality control tests and inspections to ensure accuracy and reliability of results.
• Develop and update standard operating procedures (SOPs) to meet regulatory standards.
• Investigate deviations or non-conformities, identifying root causes and implementing corrective actions.
• Train laboratory staff on quality protocols, safety procedures, and best practices to uphold quality standards.

In addition, you will carry out inspections yourself and work closely with our commercial team to ensure that our products meet customer expectations.Your ResponsibilitiesCarrying out physical inspections of fruit and vegetables.Analyzing data to improve inspections and quality controls.Working with the commercial team to understand customer requirements and translate them into inspection criteria.Developing and maintaining IT solutions to improve inspection processes.In time, travel to various locations within Europe for contact with customers, inspections and quality checks.Reporting findings and recommendations to the Head of Quality and Sustainability.Training and supervising new staff and trainees in inspection and quality processes.Preparation and maintenance of documentation and quality reports.Implementing new technologies and methodologies in the inspection process.Monitoring trends and developments within the fruit and vegetable sector in order to proactively implement quality improvements.Supporting audits and certification processes.Your ProfileExperience with or willingness to inspect fruit and vegetables.Commercial insight and ability to translate customer needs into quality standards.A foundation in IT and technical skills.Strong analytical skills and experience in data analysis.Good command of the English language, both verbally and in writing.Willingness to travel regularly, both nationally and internationally.Excellent communication and collaboration skills.Problem solving skills and attention to detail.Affinity with quality management systems and certifications (e.g.

Performing audits, supporting the Quality Manager, supporting product development..Maintaining a clean workspace..

Als Quality & Compliance Manager ontwerp, implementeer en onderhoud je Quality Management Systems (procedures).Je past Quality Risk Management (QRM) principes toe, en leidt formele management review meetings.

Als Quality & Compliance Manager ontwerp, implementeer en onderhoud je Quality Management Systems (procedures).Je past Quality Risk Management (QRM) principes toe, en leidt formele management review meetings.

Over de functie Als Quality & Compliance Manager ontwerp, implementeer en onderhoud je Quality Management Systems (procedures).Je past Quality Risk Management (QRM) principes toe, en leidt formele management review meetings.

Independently perform audits of vendors.Maintain quality oversight of vendors and performance monitoring;.Guide the teams in Change Control, Non Conformance and CAPA system;.Participate in audits and regulatory inspections;.

QUALITY

• Deputy Qualified Person for batch certification according to the Directive 2001/83/EC on medicinal products for human use and the guidelines on Good Manufacturing Practices (GMP) (Volume 4).
• Deputy RP for Good Distribution Practices (GDP) according to the Directive 2001/83/EC on medicinal products for human use and the guidelines of 5 November 2013 on GDP for medicinal products for human use.
• Review, compilation and release of batch records for administrative (GDP) release or batch certification (GMP), as appropriate.
• Completion of register of released batches (and samples).
• Quality oversight of contracted out manufacturing operations.
• Assist in the management of the distribution including import and export of medicines.
• Review and approval of transfer and validations of manufacturing and testing operations.
• Lead the drafting/approval of product specifications.
• Assist in the preparation of the quality management review at group level.
• Proactively participate as a senior quality team member in the company's QMS processes, including but not limited to deviation/investigation management, corrective and preventative actions, change control and complaints management.
• Ensure compliance with marketing authorisations / CE mark (regulatory dossier).
• Assist in the management/coordination of all activities related to a batch recall
• Proactively participate in the management of artwork and marketing/promotional materials.
• Assist in the management of stability studies and Product Quality Review.
• Ensure the compliant implementation of serialization.
• Audits & Inspections:
  • Participate in the preparation and risk assessments for the internal and external audit schedules.
  • Plan and lead external audits.
  • Participate in inspections by competent authorities as a subject matter expert.
  • Participate in self-inspections / internal audits.

Other

• Assist in local aspects of Regulatory Affairs
• Assist the Medical and Vigilance (Pharmaco and Materiovigilance) department to ensure compliance at SERB SA.
• Assist in the management of medical / scientific information requests.
• Assist in the management of advertising, samples, compliance in relation to the RP function for Belgium, Luxembourg and the Netherlands.
• Assist in the management of prices and refunds for Belgium, Luxembourg and the Netherlands.
• Monitors the regulations in force and their evolution.
• Assist for budget management.

Team management

• This role does not have reporting staff, but is expected to work within the matrix of the local (SERB SA) and wider (SERB Pharmaceuticals) quality teams as a senior member.This will include providing support, training and mentoring to the more junior members of the team as required for team development and efficient and compliant performance of the team.

QUALITY

• Deputy Qualified Person for batch certification according to the Directive 2001/83/EC on medicinal products for human use and the guidelines on Good Manufacturing Practices (GMP) (Volume 4).
• Deputy RP for Good Distribution Practices (GDP) according to the Directive 2001/83/EC on medicinal products for human use and the guidelines of 5 November 2013 on GDP for medicinal products for human use.
• Review, compilation and release of batch records for administrative (GDP) release or batch certification (GMP), as appropriate.
• Completion of register of released batches (and samples).
• Quality oversight of contracted out manufacturing operations.
• Assist in the management of the distribution including import and export of medicines.
• Review and approval of transfer and validations of manufacturing and testing operations.
• Lead the drafting/approval of product specifications.
• Assist in the preparation of the quality management review at group level.
• Proactively participate as a senior quality team member in the company's QMS processes, including but not limited to deviation/investigation management, corrective and preventative actions, change control and complaints management.
• Ensure compliance with marketing authorisations / CE mark (regulatory dossier).
• Assist in the management/coordination of all activities related to a batch recall
• Proactively participate in the management of artwork and marketing/promotional materials.
• Assist in the management of stability studies and Product Quality Review.
• Ensure the compliant implementation of serialization.
• Audits & Inspections:
  • Participate in the preparation and risk assessments for the internal and external audit schedules.
  • Plan and lead external audits.
  • Participate in inspections by competent authorities as a subject matter expert.
  • Participate in self-inspections / internal audits.

Other

• Assist in local aspects of Regulatory Affairs
• Assist the Medical and Vigilance (Pharmaco and Materiovigilance) department to ensure compliance at SERB SA.
• Assist in the management of medical / scientific information requests.
• Assist in the management of advertising, samples, compliance in relation to the RP function for Belgium, Luxembourg and the Netherlands.
• Assist in the management of prices and refunds for Belgium, Luxembourg and the Netherlands.
• Monitors the regulations in force and their evolution.
• Assist for budget management.

Team management

• This role does not have reporting staff, but is expected to work within the matrix of the local (SERB SA) and wider (SERB Pharmaceuticals) quality teams as a senior member.This will include providing support, training and mentoring to the more junior members of the team as required for team development and efficient and compliant performance of the team.

As an E&I (Electrical & Instrumentation) Supervisor, you will play a pivotal role in our technical team, responsible for overseeing a wide range of electrical and instrumentation projects.Your responsibilities will include:

• Work planning and execution: Plan, schedule, and implement electrical/instrumentation works from inception to completion, including requirements determination, deadlines setting, cost estimation, and coordination with other parties.
• Electrician and technician supervision: Manage and oversee electricians and electrical technicians, ensuring accurate, safe, and on-schedule task completion, while providing guidance and addressing issues.
• Safety compliance and risk management: Conduct regular safety inspections, identify potential hazards, implement safety procedures, and train staff to ensure compliance with safety regulations and company policies.
• Quality control: Conduct daily inspections to maintain the quality of electrical work, ensuring that installations and repairs meet industry standards and client specifications.
• Maintenance and repair: Oversee routine and preventive maintenance tasks, and repair electrical systems and equipment to minimize downtime.
• Documentation and record keeping: Maintain accurate records of all electrical work, including blueprints, schematics, maintenance logs, and inspection reports.
• Communication and collaboration: Maintain open lines of communication with team members, clients, and management, and collaborate with other departments and contractors to ensure project success.

Lead QMS activities as assigned (CAPA, audits).Participate in the QMS (ISO 9001, IATF16949,), certification process and regulatory inspection..

As a Quality Controller, your daily tasks involve conducting quality inspections, analyzing data to identify trends and areas for improvement, implementing corrective actions to address quality issues, facilitating training sessions to ensure adherence to quality standards, and collaborating with various departments to maintain a culture of quality excellence

Jobomschrijving

• Ensure compliance: Uphold regulatory standards and internal quality protocols to guarantee products meet industry regulations and customer expectations.
• Continuous improvement: Implement processes to identify areas for enhancement, driving efficiency, and minimizing defects in the production line.
• Data analysis: Analyze quality data and performance metrics to identify trends, root causes of issues, and opportunities for corrective action.
• Team collaboration: Collaborate with production teams and other departments to foster a culture of quality, providing guidance and support to ensure consistent adherence to quality standards.

Job title of the line manager: Quality Group or Customer Quality Specialist..

At their overseas sites, you are responsible for managing and executing team tasks.

As a hands-on foreman, you offer practical support in assembly, welding, and preservation.

You oversee site workers and ensure adherence to specific behavior and safety protocols.

You keep the Site Manager updated on project progress.

You coordinate tasks according to the schedule and quality standards, fostering productivity.

You perform duties in compliance with quality and safety regulations.

You identify issues and risks, reporting them to the Site Manager.

You work flexibly and can be assigned to different sites as needed.

You have first-line decision-making authority for safety and quality in the Site Manager's absence.

You handle daily coordination and consultations with the Site Manager to ensure optimal project progress.

You monitor the progress of work, focusing on quality, safety, order, and cleanliness.

Company:

For nearly a century, they have been shaping landscapes with iconic steel constructions that have an impact both nationally and internationally.

For our production site in Groot-Bijgaarden, we are looking for a vendor quality assurance engineer to support our Quality team.

Are you looking for a position where you can take the lead in the quality assurance process for our vendors and assure food safety for our clients?Do you love collaborating with internal and external stakeholders and do you like to put your problem solving skills to good use?Then this might be your next job!

Key Accountabilities

* You take the lead in the coordination of the vendor quality assurance process for our manufacturing plant in Groot-Bijgaarden.

* You take the lead in the development and maintenance of the Raw Material Monitoring plan.

* You assist the QC Manager, Purchasing and other departments in using the results of the Raw Material Risk Analysis in inspection plans and supplier agreements.

* You assist the Quality Manager in managing Raw Material related crisis's.

* You schedule and perform audits at relevant suppliers and copackers.

* You coordinate and manage vendor quality complaints.

* You create awareness on vendor quality.

* You guarantee the compliance with applicable laws and international standards regarding food safety: safety, working conditions, Hazard Analysis and Critical Control Points (HACCP), Prerequisite Programs (PRP), British Retail Consortium (BRC), Food and Drug Administration (FDA), Halal, Kosher, allergens,

As a Quality Engineer, you will analyse, develop, implement and maintain quality processes, installations and materials.

Throughout the process, you are in contact with colleagues as well as suppliers and subcontractors.

How does your responsibilities involve?

• You analyse data and implement continuous improvement initiatives to improve product quality and reliability.
• If production-related quality problems occur, you solve them: diagnoses root causes of system, process, equipment or material failures.
• In cooperation with the required team, you determine which actions should be carried out.
• You lead quality projects and are responsible for project follow-up, up to and including the final handover to the customer.
• You lead the SPC project.
• You optimize existing quality processes.
• You evaluate and design test procedures, standards and inspection techniques.
• You provide (technical) support and training to quality engineers, quality and production team leaders.
• You work with suppliers to ensure the quality of incoming materials and components.
• You prepare and follow up on quality audits.
• You report to the Business Unit Manager.

Company:

Our client is part of an industrial holding company with several global market leaders under its wing.

Innovation is central here and this also ensures a strong position in the gear systems market, in particular.This combined with a team of passionate employees ensures a true partnership with their customers.

Their high-quality solutions are used in a wide range of applications and markets (e.g.compressors, motors, pumps, scanners, railways, agricultural and construction machinery.).

The main activities for their division in the Bruges region consist of small series of gears and on the other hand the machining of large series of prismatic parts and they are specialized in aluminium parts for 30 years.

Interested in joining the team?

Safety compliance and risk management: ensure all work complies with safety regulations and company policies.This involves conducting regular safety inspections, identifying potential hazards, implementing safety procedures and training staff.

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 the position of site manager, you will be responsible for the following tasks:

• You are responsible for the technical and financial follow-up and supervision of one or more construction sites.
• You are responsible for planning and monitoring the site activities.
• You maintain regular contacts with the client.
• You manage the execution personnel by enthusing the workers and stimulating their activity.
• You control the project's quality plan during execution.

Company:

Our client is a leading company in the fields of transmission lines, wastewater treatment, swimming pool technology, industrial plants, distribution and supply lines and industrial cabling.Responding to new technologies, an eye for evolution and growing with developments in the field of piping and water treatment are the basis of their excellent reputation.

Their clients are public institutions, utilities and industrial companies.

They not only guarantee the proper installation of the connections, but also take care of the total concept if required: from engineering to execution & management, inspection and maintenance.

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
  

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
  

.· This includes, visual inspections, version control of firm and software, maintenance, and functional testing of appr equipment and accessories..

Your responsibilitiesAs a Production Manager for the spray and blast hall, you will be responsible for coordinating and managing the spray and blast hall.Together with a team of employees, you ensure the smooth operation of daily spray and blast activities.Coordination: You coordinate all daily spray and blast activities, ensuring compliance with strict quality requirements.Organization: As a Production Manager, you are responsible for your staff and the management of equipment, consumables, and machinery (e.g., scissor lifts, exhaust systems).Supervision: You lead and motivate a team of industrial painters/blast workers, supervisors, and a QC Inspector.Planning: You create a schedule and can make an accurate estimate of the number of employees, materials, and machinery required to complete the job successfully.Quality: You monitor quality and ensure work is carried out in accordance with the Inspection and Test Plan.

Hierbij neem je met de verschillende stakeholders het actieplan om en zorgt dat de oplossingen structureel geborgd worden.Je werkt samen met het ontwikkelteam om leveranciers gerelateerde kwaliteitsprestaties te bepalen en informeert de belanghebbenden.In deze functie rapporteer je aan de Plant manager.Daarnaast heb je op regelmatige basis contact met de Quality engineers in het Verenigd Koninkrijk.Wanneer nodig bezoek je de klanten om relaties op lange termijn te onderhouden (Europa).

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.