Supplier Quality Engineer (m/f/d)

at  Azenta

Hosingen, Canton Clervaux, Luxembourg -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate28 Nov, 2024Not Specified30 Aug, 20243 year(s) or aboveFrench,Government Compliance,Pareto,Instructions,High Quality Standards,Supplier Audits,Decision Making,Process Efficiency,Information Sharing,Vendor Contracts,Manufacturing,Production ProcessesNoNo
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Description:

At Azenta Life Sciences, a global leader in the life sciences space with headquarters in Burlington, MA, and offices and operations worldwide, new ideas, new technologies and new ways of thinking are driving our future. Our customer-focused culture encourages employees to embrace innovation and challenge the status quo with novel thinking and collaborative work relationships. We provide unparalleled capabilities with our lab analysis, sample management and storage services, informatics software, and consumables, with the largest installed base managing over 1 billion samples globally.
B Medical Systems, an Azenta Life Sciences company, was founded in 1979 when Electrolux partnered with the World Health Organization to create a solution for the safe storage and transport of vaccines around the world. Since that time, B Medical has become a global leader in vaccine cold chain. For over 35 years, we’ve been innovating and creating technologies that save lives across the globe.
In 2015, B Medical Systems was acquired by Navis, a private equity fund. Effective October 2022, a new chapter began and our company is a part of Azenta Inc., a leading worldwide provider of life sciences solutions.

HOW YOU’LL ADD VALUE

We are looking for a Supplier Quality Engineer (m/f/d) who carry out supplier qualification, improvement actions and quality assurance measures to purchased parts and applicable services across process steps to ensure product’s quality according to standards, securing supplies and parts for the assembly line, reviewing engineering and manufacturing specifications, monitoring materials for any defects and resolving quality issues.

ABOUT US

Azenta Life Sciences is a global life sciences leader headquartered in Burlington, MA, with offices and operation sites around the world. We are the market leader in automated biospecimen management solutions and genomic services in areas such as drug development, clinical and novel cell therapies for the world’s leading pharmaceutical, biotech, academic and healthcare institutions. Our laboratory analysis, sample management and storage, informatics software and consumables services offer unparalleled capabilities and have the largest installed base managing over one billion samples worldwide.
For more information: https://careers.azenta.com/
B Medical Systems S.à.r.l.
an Azenta Life Sciences company
17, Op der Hei
L-9809 Hosingen, Luxembourg
Christina Knappe (Senior Recruiter Central Europe)
christina.knappe@azenta.com

Responsibilities:

  • Visit vendor facilities for review and assessment of manufacturing environment, procedures and best industry practises.
  • Performing and reporting of quality control audits to ensure vendors continue to work in compliance with company and regulatory standards.
  • Follow-up of supplier audit deviations upon resolution.
  • Manage improvement and optimization of procedures to enhance supplier processes efficiency and provide guidance to reduce defect rates.
  • Manage surveillance of outsourced processes.
  • Assist and manage the supplier quality activities of development projects.
  • Conduct qualification of new purchased products according to internal procedures.
  • Evaluating and determining adequate measurement techniques and visual acceptance criteria of purchased products and services.
  • Analyse defective parts and create analysis reports.
  • Follow-up supplier claims upon resolution.
  • Coordinate containment and rework activities for purchased products .
  • Initiate and maintain continuous improvement solutions based on quality data, production inputs and customer feedback.
  • Perform problem solving and implementation of corrective actions with cross functional teams.


REQUIREMENT SUMMARY

Min:3.0Max:8.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

Graduate

Proficient

1

Hosingen, Luxembourg