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Czy chcesz otrzymywać podobne oferty pracy - "Process Manager", w miejscowości "Belgia" na email?

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25 ofert pracy dla: Process Manager lokalizacja: Belgia

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  • environment.- Good knowledge of continuous improvement or Lean methodology - Strong in data, analytics, statistics and process control. - Excellent relationship manager, influencer and communicator. - Be comfortable working in a complex international environment and willing to travel (+/- 30%) - Ability

  • colleagues and you will report to the head of quality.Responsibilities-transfer support of new products to Operations-contact suppliers & subcontractors: documentation, batch record reviewing, deviations & process validation-final product release-stability studies-customer complaint handling -CAPA

  • industry.- You are capable of taking ownership of the tasks relegated to you and able to work independent.Other informationThe offer- A challenging job with the freedom to work on your own projects- You will be involved in the whole Quality process from A – till Z - A nice salary with secondary benefits ...

  • organization and structure.Under the direction of the reporting manager, continuously strengthen quality awareness and investigate quality issues using applicable process improvement and problem solving techniques to assure successful outcomes of Company and external Health Authority

  • organisation, based in Brussels Hoofdstedelijk Gewest Belgium.The CompanyDo you want to work for an internationally oriented food specialist? Do you have an entrepreneurial mindset? And do you want to set up the entire S&OP process and department? Then please contact me for more information!Role DescriptionYour

  • reviews with the Regional Quality Leads and adapt processes, as needed.Responsibilities- Identify and define Global Processes - Drives implementation of Global Process Improvements - Establish and manage Continuous Improvement Quality ProcessesRequirements- Minimum Bachelor degree in Science or similar

  • records, deviation handling, follow-up process validation- Release of Final Products to the customer- Follow-up of stability studies- Customer Complaint Handling (Investigation, Report, Follow-up)- Initiate and follow-up CAPA reportsRequirements- Knowledge of GMP and/or ISO13485 standard- Minimum 2 years

  • developer and project developer. External stakeholders may vary from prospects and returning customers within Europe. Together with your direct colleague you will be responsible to guide to sales process from prospection to contract negotiation. You will report to the Senior Director Business Development

  • Company and external Health Authority inspections. The QC manager is reporting to the Head of Quality.Responsibilities• Management up to 12 QC chemistry and microbiology team members: (staff support, coaching, training and recruitment)• Ensuring follow-up of day-to-day activities, supervising

  • Company and external Health Authority inspections. The QC manager is reporting to the Head of Quality.Responsibilities• Management up to 12 QC chemistry and microbiology team members: (staff support, coaching, training and recruitment)• Ensuring follow-up of day-to-day activities, supervising

  • Company and external Health Authority inspections. The QC manager is reporting to the Head of Quality.Responsibilities• Management up to 12 QC chemistry and microbiology team members: (staff support, coaching, training and recruitment)• Ensuring follow-up of day-to-day activities, supervising

  • Authority inspections. The QC manager is reporting to the Head of Quality.Responsibilities• Management up to 12 QC chemistry and microbiology team members: (staff support, coaching, training and recruitment)• Ensuring follow-up of day-to-day activities, supervising implementation and progress of the QC

  • strategies to apply these regulations• Development of trainings and exchange of knowledge across teams and other departments• Leader during internal and external audits from the beginning to the end of the process, and making reports of these auditsRequirements• Bachelor of Life Sciences• Minimal 2 years of

  • strategies to apply these regulations• Development of trainings and exchange of knowledge across teams and other departments• Leader during internal and external audits from the beginning to the end of the process, and making reports of these auditsRequirements• Bachelor of Life Sciences• Minimal 2 years of

  • concepts in support of multiple projects;- You will plan and conduct scientific/laboratory experiments and evaluate and interpret data and supervise the development and validation of analytical methods (ELISA/ TCID50). You will also design and supervise in process control;- You will report results and/or

  • concepts in support of multiple projects;- You will plan and conduct scientific/laboratory experiments and evaluate and interpret data and supervise the development and validation of analytical methods (ELISA/ TCID50). You will also design and supervise in process control;- You will report results and/or

  • grown to a multinational with business in more than 100 countries. They employ over 11.000 people worldwide.Role DescriptionOur client has the vacancy of Sales Manager for their Chronic Care department. This departments contains the Ostomy Care and Continence Care branche. The Sales Manager will have

  • grown to a multinational with business in more than 100 countries. They employ over 11.000 people worldwide.Role DescriptionOur client has the vacancy of Sales Manager for their Chronic Care department. This departments contains the Ostomy Care and Continence Care branche. The Sales Manager will have

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