drjobs Sr Quality Engineer

Sr Quality Engineer

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

North Haven, CT - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Job Description:

  • The Senior Quality Engineer is responsible to represent the quality engineering function to develop and execute the strategy to organize direct and report on all supplier quality-related activities for design and manufactured items made for the AST stapling business platform.
  • Primary duties are focused on matter pertaining to supplier selection qualification manufacturing and review of technical quality documentation that includes Risk Management Documentation.

Responsibilities:

  • Lead PPAP qualifications with the CMs.
  • Collaborate with CMs to develop robust SCAPAs.
  • Support the Quality team (member of) to develop and improve an effective Supplier Quality process that supports finished goods product quality globally.
  • Work with new and existing CMs/Suppliers to develop implement and maintain technical quality assurance systems and activities including MSAs SPC Quality Plans Control Plans and FMEAs.
  • Collaborate on New Product Development (NPD) teams to evaluate and understand future CMs and their associated quality and development plans.
  • Build and own the strategy for managing the CMs/Suppliers for the business.
  • Communicate with the business Quality lead on CM initiatives updates and issues.
  • Partner with Supplier Quality Managers to build a strategy for managing the CMs in all regions.
  • Ensure CM compliance with business Quality Systems and all relevant internal procedures and policies.
  • Facilitate customer complaints for CM products and ensure adequate investigation and corrective actions are taken by CMs.
  • Manage Supplier Corrective Action Request program to ensure consistency in handling corrective actions by CMs.
  • Develop communicate and manage a strategy/plan for addressing finished goods CMs/Suppliers capability deficiencies etc.
  • Ensure proper approval and documentation practices are followed for any process material or tooling change (SCR Supplier Change Request) at CMs.
  • Define and manage the process for growing effective partnerships with preferred CMs (to drive optimal performance) founded on common interest and which demonstrate trust loyalty and financial success.
  • Lead by Example: Setting continuous-improvement driven mentality and solid quality culture for the organization.
  • Maintain compliance to set Key Performance Indicators for the business.
  • Maintain the highest level of compliance and operational standards set by the business.
  • Manage and report on CMs/Suppliers audit program in line with ISO and/or FDA 21 CFR part 820 regulations.
  • Translate engineering manufacturing and quality requirements for CM products.
  • Perform deviation investigations into quality issues arising from CM activities.
  • Manage qualifications of changes and co-ordinates associated change control activities.
  • Evaluate CMs using the appropriate CM performance management processes and develop reports on CM quality performance for company management recommend and implement the continuous improvement of CM quality systems.
  • Responsible for ensuring that effective up-to-date CM Quality Assurance documentation procedures and specifications are maintained.
  • Participate in annual supplier forums and business reviews.

Requirements:

  • Bachelors Degree in an Engineering/Scientific/Electronic or technical field.
  • Minimum 5 years experience in a Supplier Quality Quality Engineering or Reliability Engineering function.
  • Activities PPAP.
  • Design Failure Mode and Effect Analysis (DFMEA).
  • Risk management documents.
  • Supplier changes (PPAP) expertise.
  • Risk management documents.
  • Work with new and existing CMs/Suppliers to develop implement and maintain technical quality assurance systems and activities including MSAs SPC Quality Plans Control Plans and FMEAs.

Employment Type

Full-time

Company Industry

About Company

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.