Celestica

Operations Quality Specialist

Celestica

full-time

Posted on:

Location Type: Office

Location: Galway • 🇮🇪 Ireland

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Job Level

Mid-LevelSenior

Tech Stack

PMP

About the role

  • Mentors and develop personnel in the practices of Quality management and Quality improvement
  • Lead the team to investigate any quality excursions and implement corrections and corrective actions
  • Lead the quality group in a fast-paced production environment
  • Customer liaison for quality escalations and daily quality issues ensuring measured, developed and timely responses to the customer
  • Support the change management process and Customer requests as appropriate
  • High level of competence using relevant corrective action systems (e.g CAPA)
  • Create concise and accurate technical reports, communicate results and manage subsequent analysis queries
  • Continually seek to drive improvements in product and process quality
  • Create and evaluate metrics to drive the quality improvement processes
  • Own, Maintain and report timely and accurate KPI’s
  • Manage and maintain the NCMR database and report weekly to the customer
  • Using appropriate statistical techniques to monitor process performance (e.g.SPC, Minitab, Ppk, Gage R & R analysis, sampling techniques)
  • Provide quality engineering support to the facility, including validation and risk management and review of technical documentation (eg. FMEA’s, control plans)
  • Apply project management skills and methodology as necessary for key CI projects

Requirements

  • Strong knowledge of quality tools, ISO / QMS standards and processes (ISO 9001, ISO13485)
  • Knowledge of data analysis and presentation software and its uses in generating reports, capturing data and presenting data in an understandable format
  • Strong knowledge of product and manufacturing processes and materials properties
  • Knowledge of quality tools such as FMEA, PMP, SPC, 8D methodology, etc.
  • Knowledge of Six sigma and Lean Kaizen
  • Ability to effectively communicate with a wide variety of internal and external customers to summarize complex technical issues
  • Knowledge of Med-tech and regulatory requirements (such as FDA and MDR) is a requirement of the role with pharma & medical device systems an advantage
  • Ability to effectively lead and manage several projects simultaneously and coordinate multiple, changing deadlines while also working effectively on their own and in a team environment
  • Ability to be an Internal Auditor
  • Experience in a Med-tech environment is essential
  • Experience of 6 Sigma quality methods would be a distinct advantage
  • Materials engineering experience/quality materials testing knowledge is an advantage
  • Experience of leading a team is an advantage
Benefits
  • Market-competitive total reward: flexible salary, fix and variable salary based on goals
  • The opportunity to become a key member of the new product introduction team in the Health Tech.
  • Quality function driven by innovation where creativity matters
  • Training and development opportunities, with us the sky is the limit
  • The opportunity to innovate, learn, mentor others and work toward your own vision of career success
  • A global, collaborative culture with strong leadership imperatives to foster your growth and professional opportunities
  • A sustainable culture where we provide opportunities for employees to give back to the community

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills
quality managementquality improvementcorrective action systemsstatistical techniquesdata analysisFMEASPCSix SigmaLean Kaizenproject management
Soft skills
mentoringcommunicationleadershipteam managementcustomer liaisonproblem-solvinganalytical thinkingtime managementadaptabilitycollaboration
Certifications
Internal Auditor certification