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Publié il y a 26 jours

Process Quality Engineering Team Lead - Operations (Hybrid)

@ Kardium Inc.

Burnaby, Colombie-Britannique

102k–120k $/an5+ ans d’expérience
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En bref

Kardium Inc. is hiring a Process Quality Engineering Team Lead for Operations in Burnaby, BC, on a full-time permanent hybrid basis. The role leads a team resolving quality issues in Catheter/Introducer subassembly, covering non-conformance disposition, rework and continuous improvement across two shifts. Compensation is $102,000 to $120,000 annually including base salary and a 5% RRSP contribution.

Salaire :

102 000 $–120 000 $ par année

Responsabilités :

  • Lead and coordinate process quality professionals on two shifts
  • Lead investigations and determine disposition of non-conforming products
  • Drive continuous improvement and systemic quality investigations
  • Build partnerships with Quality Control, Engineering and Manufacturing
  • Train and mentor manufacturing team members

Résumé des exigences :

  • At least 5 years quality control experience in multi-disciplinary manufacturing
  • Medical device manufacturing and quality control experience
  • Proven experience with non-conformances and root-cause analysis
  • Knowledge of statistics, SPC, FMEA and process capability
  • Excellent technical communication and interpersonal skills

Outils et compétences

Avantages mentionnés

Soins dentairesRégime de retraiteCongé parentalOptions d’achat
Source et dates

Site carrière / système de candidatures · dayforce-feed

Date publiée par l’employeur
2026-10-15
Première détection par notre source
2026-10-16
Mise à jour du dossier source
2026-10-30

Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.

Détails du poste

NiveauChef d’équipe
DomaineAssurance qualité
Expérience5 an(s) et plus
Gestion d’équipeOui
Heures par semaine40 (estimé)
Milieu de travailUsine, Bureau
PositionAssis et debout
Exigences physiquesphysique faible · ordinateur modéré
LanguesEnglish
Avantages mentionnésCongé parental généreux, Régime de retraite, Actions ou participation, Mieux-être

Résumé et détails rédigés par l’IA à partir de l’offre; l’offre de l’employeur fait foi.

Kardium Inc.

Profil d’entreprise sauvegardé

Renseignements historiques provenant d’un profil The Jobs API sauvegardé (champs LinkedIn/Crunchbase). Ils ne sont pas vérifiés en temps réel; les chiffres peuvent avoir changé. Les valeurs manquantes restent inconnues.

Description complète de l’entreprise

Kardium has developed the Globe System - a revolutionary medical device for the diagnosis and treatment of atrial fibrillation. .

Abonnés LinkedIn
24 402
Personnes associées sur LinkedIn
603
Bureaux déclarés
  • 8518 Glenlyon Pkwy, 155, Burnaby, BC V5J 0B6, CA
Catégories d’activité
  • Health Diagnostics
  • Medical Device
  • Hardware
  • Medical
  • Manufacturing
Autres noms enregistrés
  • Kardium Inc.
Le profil indique une agence de recrutement
Non
Investissement total déclaré
470 310 055

La devise et la date d’observation ne sont pas fournies; ce n’est ni une valorisation actuelle ni une ronde de financement.

Kardium has developed the Globe System - a revolutionary medical device for the diagnosis and treatment of atrial fibrillation. .

ChampValeur
SecteurMedical Equipment Manufacturing
Taille501-1,000 employees
Siège socialBurnaby, BC
Type d’organisationPrivately Held
Fondée en2007
Offres sur Jobsy7
LinkedInVoir la page
Description


Title: Process Quality Engineering Team Lead – Operations
Employer: Kardium Inc.
Location: 155–8518 Glenlyon Parkway, Burnaby, BC V5J 0B6
Employment: Full-time, permanent
Compensation: $102,000–$120,000 annually, including base salary and a 5% RRSP contribution
Benefits: Stock options; medical and dental coverage; three personal days per year; employee and dependent well-being support; career development, learning, and professional membership support; maternity and adoptive leave top-up; and fertility drug coverage
Workplace Language: English

Your opportunity

Join Kardium in improving the lives of millions through our ground-breaking device for diagnosing and treating atrial fibrillation, a common heart rhythm disorder that can lead to stroke, heart failure, and other complications.

As Process Quality Engineering Team Lead – Operations, you will lead a team resolving quality issues in Catheter/Introducer subassembly processes, with a focus on non-conformance disposition and rework. You will be the primary contact for production quality concerns across two shifts.

Responsibilities

  • Develop a detailed understanding of Kardium’s products and manufacturing processes and apply that knowledge proactively when overseeing production quality activities, investigations, and process improvements
  • Lead and coordinate the day-to-day activities of process quality professionals in a fast-paced manufacturing environment, including assigning, prioritizing, and scheduling operational and project work to meet production needs
  • Lead investigations with subject matter experts, review non-conforming products and materials, determine their disposition, and resolve production quality issues affecting assembly and subassembly work
  • Support and drive continuous improvement initiatives, including investigations into systemic product quality issues and recommendations to improve manufacturing processes, workflow, and productivity
  • Build and maintain strong cross-functional partnerships with Quality Control, Engineering, Manufacturing, and Quality Assurance to coordinate production quality activities and address operational priorities
  • Train and mentor manufacturing team members on job responsibilities, quality procedures, safety requirements, and company policies, and provide input on staffing and personnel decisions
  • Design, implement, and continuously improve processes for monitoring, evaluating, and reporting on product quality trends, process performance, and production quality activities

Qualifications

  • At least 5 years of quality control experience in a multi-disciplinary manufacturing environment
  • Manufacturing and quality control experience in medical device production
  • Proven experience with non-conformances, failure investigations, root-cause analysis, and other quality assurance tools
  • Demonstrated knowledge of statistics and concepts such as SPC, FMEA, process capability.
  • Excellent technical communication and interpersonal skills, with a proven ability to build consensus among diverse stakeholders


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