More jobs:
Senior Quality Engineer - Product Transfer
Job in
Germany, Pike County, Ohio, USA
Listed on 2026-01-13
Listing for:
Stryker Corporation
Full Time, Contract
position Listed on 2026-01-13
Job specializations:
-
Quality Assurance - QA/QC
Quality Engineering -
Engineering
Quality Engineering, Process Engineer
Job Description & How to Apply Below
Location: Germany
Senior Quality Engineer - Product Transfer (fixed-term contract) page is loaded## Senior Quality Engineer - Product Transfer (fixed-term contract) locations:
Isere, Montbonnot-Saint-Martin 176 Rue Lavoisier:
Cork, Carrigtwohill Anngrove North SEO:
Freiburg, Germ anytime type:
Full time posted on:
Posted 3 Days Agojob requisition :
R555556
Work Flexibility:
Hybrid Within the
** QA Shared Services – Product Transfer
** team, you will play a key role in the successful execution of
** global manufacturing transfers**. You will ensure regulatory compliance, support validation activities, and contribute to continuous improvement initiatives to deliver efficient transfers in terms of
** quality, cost, and timelines**.This is a 1-year fixed-term contract as part of a maternity leave replacement, with the possibility of extension.##
** Key Responsibilities*** ##
** Support all types of manufacturing transfers**, including supplier-to-supplier, supplier-to-Stryker, Stryker-to-supplier, and inter-site Stryker transfers
* Review and approve
** validation and qualification documentation
*** Act as the
** Quality Assurance point of contact
** during scope definition, planning, and execution of supplier transfers
* Provide quality guidance related to applicable
** regulations, standards, and procedures
*** Identify potential
** quality risks
** during transfers and propose effective mitigation solutions
* Collaborate with multiple divisions (T&E, Joint Replacement, Endoscopy) and contribute to
** quality best practices
** across the organization##
** Candidate Profile**##
** Required Qualifications
*** University degree in
** Engineering, Science or a related field
*** Minimum
** 2 years of experience
** in Quality Assurance and validation, preferably in the
** medical device or pharmaceutical industry
*** Strong knowledge of
** quality concepts, risk management tools, and regulatory standards** (ISO 13485, FDA 21 CFR Part 820)
* ** Fluent in English**##
** Preferred Qualifications
*** Experience with
** Quality Management Systems (QMS)
** or
** Supplier Quality
*** Excellent
** communication, presentation, and project management skills**, with strong attention to detail
* ** Lean Six Sigma certification** (ideally Green Belt)
Join an international and regulated environment, at the heart of high-impact quality transfer projects, contributing directly to the improvement of healthcare.
Travel Percentage : 10%
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Position Requirements
10+ Years
work experience
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