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Première détection par notre source: il y a 1 heure

Open Role (5 Positions): Industrial Automation and CSV Engineer - Ontario, Canada (Cambridge)

@ VTI Life Sciences

Ontario

Contrat6+ ans d’expérience
Postuler
SIGNAUX

En bref

VTI Life Sciences is hiring up to five contract Senior Automation Validation Engineers for a project on automated and robotic medical-device assembly equipment in Cambridge, Ontario. The work covers hands-on validation and testing of PLC and SCADA controlled systems, including Software V&V, FAT and SAT protocols. The contract runs October 26, 2026 through January or February 2027, about 14 billable weeks, with possible extension.

Responsabilités :

  • Write, review and execute Software V&V, FAT and SAT protocols
  • Test PLC logic, interlocks, alarms and recovery conditions
  • Verify device assembly and equipment functional testing
  • Confirm part traceability and data integrity
  • Document results, discrepancies and deviations

Résumé des exigences :

  • Six years of PLC and SCADA automation experience
  • Four years of validation in a regulated manufacturing environment
  • Hands-on Rockwell Automation and FactoryTalk View experience
  • Knowledge of the software V&V lifecycle
  • Ability to read PLC logic and electrical drawings

Outils et compétences

Source et dates

Type de source non vérifié · apify-linkedin

Date publiée par l’employeur
Non fourni
Première détection par notre source
2026-11-15
Mise à jour du dossier source
2026-11-15

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

Détails du poste

NiveauSenior
DomaineAssurance qualité
Expérience6 an(s) et plus
Déplacementsavion : aucun · route : aucun
Milieu de travailUsine, Laboratoire
PositionAssis et debout
Exigences physiquesphysique faible · ordinateur élevé
LanguesEnglish

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

VTI Life Sciences

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.

VTI is a consulting firm specializing in automation and CQV services to biotech, pharmaceutical, and med device clients.

Description complète de l’entreprise

VTI Life Sciences is an ISO 9001:2000 Certified Company with the experience, expertise, and commitment to provide the superior service required to meet all of your validation and compliance needs. We offer a full spectrum of services including: computer validation, cleaning validation, process validation, clean room certification, temperature mapping, process equipment and facility qualification, and much more. Dedication to quality, personalized support and the success of your projects are the foundation of our company. VTI Life Sciences has offices located in San Diego, San Francisco, Boston, and China.

Abonnés LinkedIn
6 120
Personnes associées sur LinkedIn
53
Bureaux déclarés
  • 10815 Rancho Bernardo Road, Suite 120, San Diego, California 92127, US
  • 10815 Rancho Bernardo Road, Suite 120, San Diego, CA 92127, US
  • 10815 Rancho Bernardo Road, Suite 120, San Diego, CA 92127, US
  • 10815 Rancho Bernardo Road, Suite 120, San Diego, CA 92127, US
  • 10815 Rancho Bernardo Road, Suite 120, San Diego, CA 92127, US
Autres noms enregistrés
  • VTI Life Sciences
Spécialités
  • Computer Validation
  • Commissioning & Qualification (C&Q)
  • Cleaning & Process Validation
  • Project Management
  • Automation & Control Systems
  • IT Services
  • Calibration
  • Process Equipment & Facility Qualification
  • Quality & Regulatory Services
  • and Temperature Mapping
Le profil indique une agence de recrutement
Non
Investissement total déclaré
0

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

VTI Life Sciences is an ISO 9001:2000 Certified Company with the experience, expertise, and commitment to provide the superior service required to meet all of your validation and compliance needs. We offer a full spectrum of services including: computer validation, cleaning validation, process validation, clean room certification, temperature mapping, process equipment and facility qualification, and much more…

ChampValeur
SecteurBiotechnology
Taille51-200 employees
Siège socialSan Diego, California
Type d’organisationPrivately Held
Fondée en1996
SpécialitésComputer ValidationCommissioning & Qualification (C&Q)Cleaning & Process ValidationProject ManagementAutomation & Control SystemsIT ServicesCalibrationProcess Equipment & Facility QualificationQuality & Regulatory Servicesand Temperature Mapping
Offres sur Jobsy1
LinkedInVoir la page
Description

Engagement: Contract, with possibility of extension

Anticipated term: October 26, 2026 through January / February 2027

Duration: Approximately 14 billable weeks, allowing for two non-billable weeks during the winter holidays

Position Summary

We are seeking experienced Senior Automation Validation Engineers to support our project involving automated and robotic medical-device assembly equipment.

The successful candidates will provide hands-on validation and testing support for PLC and SCADA controlled manufacturing systems. This role requires strong knowledge of medical device assembly, industrial controls, automation architecture familiarity, equipment functionality, computerized system validation, data integrity, and regulated manufacturing practices.

Candidates must be local to the Cambridge, Ontario area or willing to temporarily relocate for the duration of the assignment. Routine travel expenses are not anticipated.

Key Responsibilities

• Edit, review, dryrun, and execute Software V&V, FAT and SAT protocols for Automated Machinery equipment.

• Plan and perform software verification and validation activities throughout the system lifecycle.

• Test PLC logic, equipment sequences, interlocks, alarms, error codes, system messages, and recovery conditions.

• Execute feature, unit, integration, functional, and User Acceptance Testing.

• Challenge sensors, actuators, electrical controls, safety devices, vision systems, and robotic equipment.

• Verify device assembly processes and equipment-based functional testing.

• Confirm part traceability, electronic records, database transactions, and system data flows.

• Assess data integrity controls in accordance with regulated-industry expectations.

• Review PLC and SCADA configurations, automation architecture, control, and electrical documentation.

• Document test results, discrepancies, objective evidence, and deviations with a high level of accuracy.

• Collaborate and establish excellent rapport and communication with equipment suppliers, controls engineers, quality, manufacturing, and project stakeholders.

• Support troubleshooting, deviation resolution, corrective actions, and protocol closeout.

Required Qualifications

• Minimum of six years of experience working with PLC and SCADA controlled industrial automation or assembly equipment.

• Minimum of four years of experience working in validation in a regulated manufacturing environment.

• Demonstrated expertise reviewing, editing, authoring and executing Software V&V, FAT, SAT protocols.

• Strong understanding of the software verification and validation lifecycle.

• Knowledge of PLC programming concepts and industrial automation architecture.

• Hands-on experience with working with the Rockwell Automation suite and FactoryTalk View.

• Experience testing equipment alarms, error codes, interlocks, system messages, and abnormal operating conditions.

• Working knowledge of electrical panels, controls, sensors, actuators, vision systems, and robotic machinery.

• Experience with databases, electronic records, part-traceability systems, and data-integrity principles.

• Ability to interpret PLC logic, electrical drawings, functional specifications, and equipment design documentation.

• Strong technical writing, troubleshooting, and cross-functional communication skills.

Strongly Preferred

• Medical-device assembly or manufacturing experience.

• Experience validating automated or robotic medical-device assembly lines.

• Experience with Ignition SCADA environments.

• Familiarity with GxP practices, computerized system validation, and applicable medical-device quality requirements.

• Experience validating vision inspection, device functional testing, serialization, or part-traceability systems.

Assignment Requirements

• Must be available to work onsite in Cambridge, Ontario.

• Candidates must already be local or willing to relocate temporarily to avoid recurring travel expenses.

• Two weeks of non-billable time are anticipated during the winter holiday period.

  • • Strong performers may be considered for an extension beyond the initial project stage.
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