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Job ID :
46906BR
Location :
Germany - Braunschweig
:
Job Description
A long tradition, international experience, high quality standards and a wide product portfolio are the ingredients to what makes us one of the leading manufacturers of slides and specialty glass.
For over 60 years Menzel Gläser has been manufacturing laboratory glass supplies that have been used in medicine, biology and research.

For this site in Braunschweig we are looking for a

Supervisor quality engineer (f/m)

Job Duties and Responsibilities:
  • Responsible for Quality Assurance at the manufacturing site in Braunschweig, Germany.
  • Development and optimization, and maintenance of the quality system in compliance with the corporate standards and industry standards
  • Lead investigation, closure and tracking of customer complaints.
  • Maintain Corrective Action System to analyze and correct nonconforming conditions and drive problem solving activities to identify and correct root cause.
  • Supervises the daily quality operations and ensures continuous compliance to procedures, with special focus on problem solving, nonconformances handling, out of specification results, and CAPAs.
  • Responsible to complete in a timely manner all reports and trend analyses related to quality.
  • Maintain a Quality Organization at the cutting edge by anticipating and identifying customer needs and priorities and integrating them into the Quality System
  • Act as registered Security Officer and interface with the BfArM (FDA) the German regulatory authorities for medical devices.
  • Interact both vertically and horizontally in a way that commands both personal respect and mission acceptance and possess the ability and interpersonal skills to influence all levels of the organization. Interact with Customers and Suppliers, when required, applying these same attributes as required to promote external relationships and properly represent the interests of Thermo Fisher Scientific.
  • Promote PPI approaches with a quality principled focus that includes Daily Standard Work and continuous disciplined focus on processes.
  • Communicate customer, regulatory and organizational requirements to assure product quality, contract compliance and customer satisfaction
  • Act as a change agent for improvement initiatives
  • Create and maintain both a Quality-centric and Quality-focused culture for all production activities
  • Perform all job duties in a safe manner and obey all safety policies and procedures
  • Perform as a Role Model Leader, acting in compliance with the Thermo Fisher Code of Ethics and the 4-I Values (Integrity, Intensity, Involvement and Innovation).
Requirements:
  • A minimum of a Bachelor Degree in an appropriate degree in combination with comprehensive knowledge of manufacturing processes is required. A degree in Engineering, Quality Management, Bio-medical or related field is preferred.
  • Minimum two years of experience with manufacturing companies producing medical products
  • Experience in International Standards ISO-9001, ISO-13485: and 21 Code of Federal Regulations (CFR), Quality Systems Regulation (QSR) preferred
  • Experience in world class Quality practices including LEAN Leadership methodologies, root cause analysis, preventative action deployment and quality function tools preferred
  • Fluent in written and spoken English
  • Proficiency in Microsoft Office including Excel, Word, and PowerPoint
  • Able to travel (domestic and international) up to 20%
We offer:
  • Employment with an innovative, future-oriented organisation
  • Outstanding career and development prospects
  • Company pension scheme and other fringe benefits
  • Exciting company culture which stands for integrity, intensity, involvement and innovation
*IND-EMEA


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