András Vámos

András Vámos Email and Phone Number

Head of Quality at Diatron Medical Instruments @ Diatron Medical Instruments
budapest, budapest, hungary
András Vámos's Location
Budapest, Budapest, Hungary, Hungary
András Vámos's Contact Details

András Vámos work email

András Vámos personal email

About András Vámos

András Vámos is a Head of Quality at Diatron Medical Instruments at Diatron Medical Instruments. They possess expertise in iso 13485, medical devices, capa, quality system, validation and 17 more skills. They is proficient in Hungarian and English. Colleagues describe them as "There are leaders and bosses - and there is András. Please take your time and imagine a man being purposive, determined, empathic and reasonable at the same time. Who really can find the razorblade-widened border of employee satisfaction and businnes realated goals: walking by, never tilting - just reaching the top. Who always has the enthusiasm to make the best team to reach the highest grounds - and over. You could have an image about a leader, a boss like that. I had, and now I… Show more" and "It is a true pleasure to recommend András. He was one of our QA engineer, who had grown up in his profession at our company, targeted leadership and became a Quality Manager of one of our mass-production site. He also tried Operation Manager position for a while and gained lots of manufacturing, QA, lean and leadership experience. Beside of his high level technical knowledge, he is a favoured manager of his team and a very good partner for inspiring dialogues. He has both… Show more"

András Vámos's Current Company Details
Diatron Medical Instruments

Diatron Medical Instruments

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Head of Quality at Diatron Medical Instruments
budapest, budapest, hungary
Website:
diatron.com
Employees:
117
András Vámos Work Experience Details
  • Diatron Medical Instruments
    Head Of Quality
    Diatron Medical Instruments Jan 2018 - Present
    Budapest, Budapest, Hungary
    - Lead the quality and regulatory affairs team (Managing 31 staff) – Quality Engineering, SQA, Quality Control, Quality System, Regulatory Affairs, NPI Quality, EHS- Maintain compliance and continuously improve the Diatron QMS in regard to ISO 9001, ISO 13485, 21 CFR PART 820, IVDD 98/79 EC, IVDR 2017/746 and further regulatory requirements which apply to the Diatron product portfolio- Act as PRRC (Person Responsible for Regulatory Compliance) as defined in IVDR 2017/746- Establish strategy and manage projects related to QMS and process harmonization between HQs and Diatron- Continuously analyze quality management system processes and drive improvement actions across the whole organization- Define quality management system goals and ensure alignment with other relevant business goals of Diatron
  • Diatron Medical Instruments
    Quality Manager
    Diatron Medical Instruments Mar 2017 - Dec 2017
    Budapest, Budapest, Hungary
  • Thalesnano Inc.
    Technical Operations Director
    Thalesnano Inc. Aug 2015 - Mar 2017
    Budapest
    • Lead the following departments: Production, Logistics, Quality and Warehouse (Managing 11 staff)• Ensure cost effective operation of the company: production planning and its alignment to sales, inventory management and reduction, identification and management of cost reduction activities• Ensure robust quality management system by establish the following quality functions: SQA, QS, incoming and finished product QC. Implement metrics and feedback system• Continuously evaluate the effectiveness of the departments and manage improvement activities using LEAN tools with special focus on logistics (base data, procurement, shipping, production planning and stock accuracy)
  • Bd Hungary
    Production Quality Leader
    Bd Hungary Jun 2013 - Aug 2015
    Tatabánya
    • Led the following Quality functions: Production Quality Engineering, Batch Release, Microbiology, Quality Control: Incoming Material Control and Finished Product Control (Managing 46 staff)• Ensured efficiency of PQA functions by analyzed, challenged and improved their performance• Continuously monitored and improved the quality management processes of the different production areas• Ensured compliance with ISO 9001, ISO 13485, FDA and relevant cGMP regulations
  • Coloplast A/S
    Senior Sqa Manager
    Coloplast A/S May 2012 - May 2013
    Humlebæk, Denmark
    • Ensured compliance to national/international quality standards of supplier processes• Quality approval of suppliers: Performed audits, negotiated and approved quality agreements• Managed improvements tasks/projects at suppliers• Managed/reviewed CAPA including root cause analysis on Supplier related tasks and gave input to STC Quality• Designed, reviewed and updated of SQM Key processes in connection with changes to existing materials, intermediates and products and ensured these were aligned with related areas and company business• Specialist level on Supplier Quality Management, audit types (including link to business and ethic and decision board) and acted as mentor for other global supplier specialists in the organization and transfered knowledge by training
  • Coloplast Hungary Ltd
    Head Of Quality
    Coloplast Hungary Ltd May 2010 - May 2012
    Nyírbátor
    • Overall responsibility for quality and regulatory compliance of the Nyírbátor Site according to the corporate and international quality standards• Ensured that the quality system supports the business development and efficiency of the Site• Led the following Quality functions: Operative Quality Engineering, Validation, Microbiology, Incoming Material Control, Customer Complaints Handling, EHS, Supplier Quality Assurance (Managing 22 staff)
  • Coloplast Hungary Ltd
    Head Of Operations
    Coloplast Hungary Ltd Jul 2009 - May 2010
    Nyírbátor
    • Led the Nyírbátor Site’s manufacturing and warehouse functions (6 Value Streams) so that all production activities met the organization’s business objectives and were conducted in accordance with the relevant health & safety, environmental and quality standards• Contributed to strategic planning and decision-making at Site management level• Monitored the cost and effectiveness of production activities to optimize resources, prioritize spending and achieve volume, quality and manufacturing standards
  • Coloplast Hungary Ltd
    Quality Leader
    Coloplast Hungary Ltd Nov 2007 - Jul 2009
    Nyírbátor
    • Established the quality management system from the beginning of the operation at the Site according to the corporate quality standards• Led the Operative Quality Engineering and Validation functions• Hired the Quality staff• Provided support for successful incoming transfers from quality point of view• Quality support for production processes
  • Coloplast Hungary Ltd
    Quality Engineer
    Coloplast Hungary Ltd Aug 2004 - Nov 2007
    Tatabánya
    • Kept continuous control and improved the quality management processes of the Value Stream• Ensured compliance with ISO 9001, ISO 13485, FDA and Japanese regulations• Issued, updated and distributed quality instructions and forms• Organized quality training• Handled quality related activities of machine and process transfers from Denmark• Investigated customer complaints and took corrective and preventive actions• Analyzed and evaluated non-conformities
  • Gedeon Richter Pharmaceutical Ltd.
    Plant Mechanical Engineer
    Gedeon Richter Pharmaceutical Ltd. Jul 2001 - Aug 2004
    Budapest
    • Organized and controlled maintenance activities; SAP PM module• Kept contact with suppliers in connection with maintenance projects• Assumed responsibility for qualification documentations of machines and supply systems
  • Gedeon Richter Pharmaceutical Ltd.
    Validation Engineer
    Gedeon Richter Pharmaceutical Ltd. Sep 1998 - Jul 2001
    Budapest
    • Established the system of verification of HVAC systems for clean rooms• Performed validation activities of HVAC system of clean rooms and laminar air flow units, nitrogen and compressed air supply systems

András Vámos Skills

Iso 13485 Medical Devices Capa Quality System Validation Quality Management Quality Assurance Manufacturing Quality Control Continuous Improvement Fda Process Improvement Iso 9000 Lean Manufacturing Quality Auditing Fmea Change Control Gmp Root Cause Analysis Value Stream Mapping Iso Pharmaceutical Industry

András Vámos Education Details

  • Budapest University Of Technology And Economics
    Budapest University Of Technology And Economics
    Faculty Of Mechanical Engineering, Department Of Chemical And Food Engineering
  • Budapest University Of Technology And Economics
    Budapest University Of Technology And Economics
    Institute Of Continuing Engineering Education

Frequently Asked Questions about András Vámos

What company does András Vámos work for?

András Vámos works for Diatron Medical Instruments

What is András Vámos's role at the current company?

András Vámos's current role is Head of Quality at Diatron Medical Instruments.

What is András Vámos's email address?

András Vámos's email address is hu****@****ast.com

What schools did András Vámos attend?

András Vámos attended Budapest University Of Technology And Economics, Budapest Business School, Budapest University Of Technology And Economics.

What are some of András Vámos's interests?

András Vámos has interest in Capa Management.

What skills is András Vámos known for?

András Vámos has skills like Iso 13485, Medical Devices, Capa, Quality System, Validation, Quality Management, Quality Assurance, Manufacturing, Quality Control, Continuous Improvement, Fda, Process Improvement.

Who are András Vámos's colleagues?

András Vámos's colleagues are Kitti Kemény, Kata Götz, Bernadett Bartók, Gábor Széplábi, Imre Kálmán, Szabolcs Gonda, Attila Fizil.

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