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68 jobs voor Compliance Officer gevonden in Brussel (Regio)

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Compliance Conduct and Risk Expert

WALTERS PEOPLE in BRUSSEL
time Online sinds 28 juni 2024 - Tijdelijke jobs met optie vast

A leading company is actively seeking a driven Compliance Conduct and Risk Expert to join their offices in Brussels.Your seasoned experience in Compliance makes you the perfect fit for this pivotal role within the organization.

As a cornerstone of the team, you will play a critical role in the evolution of legislation and regulations across various compliance domains, such as: investor protection, product governance, advertising and publicity for banking and investment products, protection rules for borrowers, conflicts of interest, complaint handling, Privacy, inside information and market abuse.

Your expertise will not only contribute to the success of different projects but also ensure that the company remains at the forefront of industry standards.

Your main responsibilities as the new Compliance Conduct and Risk Expert will include:

  • Following relevant laws and regulations and ensuring that internal policies, procedures and guidelines for head office and agents are in place and updated in a timely manner
  • Analysing these laws and regulations, and in the event of shortcomings, informing management together with the compliance officer and developping action plans
  • Following up on the action plans and reporting on this to the compliance officer
  • Following up the implementation projects of legislation and regulations, and providing advice on various proposals from the operational services
  • Validating your investment product and commercial training from the point of view of the compliance domains
  • Representing the compliance function in committees and working groups, and participating in internal and external compliance reporting

Legal / Ethics & Compliance Officer - International role - BXL

MICHAEL PAGE in BRUSSEL
time Online sinds 8 juni 2024 - Vaste jobs
  • You are in charge of conducting internal controls and audits to verify the implementation of the compliance programs in all our entities worldwide related to ethics (including anti corruption / human rights), data protection and corporate governance;
  • You interact with the different entity ethics, legal and data protection officers/managers to organize, conduct and follow up on the internal controls and audits;
  • You prepare internal control and audit reports with action plans and follow up on implementation of the actions;
  • You contribute to the ISO 37001 audit and certification process; follow up of action plans to address non-conformities and observations;
  • You identify compliance and internal control deficiencies, recommend actions to rectify, implement if applicable and follow up these actions;
  • You communicate findings and recommendations to improve the compliance programs and internal processes to address risks, determine root causes, propose an action plans for remediation in a timely manner, implement actions if applicable and track findings through resolution;
  • You follow up compliance actions, consolidating data and producing reports;
  • You develop and manage working relationships with key stakeholders;
  • You propose an annually internal control and audit program of processes and controls reviews, made to give reasonable assurance of the quality of the self-assessments made by the Business Process Owners (BPOs);

Internal Interfaces

  • Internal Control and Audit to whom you will report functionally;
  • Group's Internal Control and Internal Audit functional lines;
  • Entity and group compliance teams;
  • Managers, business and support line teams;
  • ICCs (Internal Control Coordinators), BPOs (Business Process Owners) and/or other internal control representatives within our client's Business Areas;
  • Corporate Risk Officer;
  • Purchasing Officer;
  • Quality.

External Interfaces

  • External auditors.

Legal / Ethics & Compliance Officer - International role - BXL

MICHAEL PAGE in BRUSSEL
time Online sinds 8 juni 2024 - Vaste jobs
  • You are in charge of conducting internal controls and audits to verify the implementation of the compliance programs in all our entities worldwide related to ethics (including anti corruption / human rights), data protection and corporate governance;
  • You interact with the different entity ethics, legal and data protection officers/managers to organize, conduct and follow up on the internal controls and audits;
  • You prepare internal control and audit reports with action plans and follow up on implementation of the actions;
  • You contribute to the ISO 37001 audit and certification process; follow up of action plans to address non-conformities and observations;
  • You identify compliance and internal control deficiencies, recommend actions to rectify, implement if applicable and follow up these actions;
  • You communicate findings and recommendations to improve the compliance programs and internal processes to address risks, determine root causes, propose an action plans for remediation in a timely manner, implement actions if applicable and track findings through resolution;
  • You follow up compliance actions, consolidating data and producing reports;
  • You develop and manage working relationships with key stakeholders;
  • You propose an annually internal control and audit program of processes and controls reviews, made to give reasonable assurance of the quality of the self-assessments made by the Business Process Owners (BPOs);

Internal Interfaces

  • Internal Control and Audit to whom you will report functionally;
  • Group's Internal Control and Internal Audit functional lines;
  • Entity and group compliance teams;
  • Managers, business and support line teams;
  • ICCs (Internal Control Coordinators), BPOs (Business Process Owners) and/or other internal control representatives within our client's Business Areas;
  • Corporate Risk Officer;
  • Purchasing Officer;
  • Quality.

External Interfaces

  • External auditors.

Technical supervisor EN/FR

MANPOWER BELGIUM in BRUSSEL
time Online sinds 12 april 2024 - Vaste jobs
Maintaining excellence: Ensuring that all areas of the property are maintained to the highest level to guarantee compliance with company standards Optimizing the customer experience: Leading a responsive and positive team to ensure customer satisfaction and comfort by effectively responding to their needs Implementing strategies: Supporting and implementing department strategies and objectives, assuming specific responsibilities and replacing the manager in their absence Cultural leadership: Playing a key role in promoting a culture of growth, development, and performance, while embodying the company's values Cost and inventory control: Collaborating to keep costs under control and achieve desired productivity levels Interpersonal relationships: Establishing and maintaining effective relationships with internal and external stakeholders, ensuring smooth and timely communication Proactive management: Managing the preventive maintenance program to ensure environmental sustainability and asset preservation Legal compliance: Ensuring legal compliance and documenting best practices for internal and external audits Company:Are you looking for a new challenge in the hospitality industry?Our client is a well known international company in the industry, providing exceptional accommodation experiences to their visitors in Saint Gilles.They are committed to ensuring that every detail is taken care of for their guests' comfort and satisfaction.

Senior Quality Assurance Officer

SERB NV in ELSENE
time Online sinds 19 juni 2024 - Vaste jobs

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.

Senior Quality Assurance Officer

SERB NV in ELSENE
time Online sinds 19 juni 2024 - Vaste jobs

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.