Publié il y a 2 mois
Industrial Automation and CSV Engineer - Ontario, Canada
@ VTI Life Sciences
Cambridge, Ontario
En bref
VTI Life Sciences is hiring a Senior Automation Validation Engineer on a contract basis in Cambridge, Ontario, with a possible extension. The work covers validating PLC and SCADA controlled medical-device assembly equipment, including FAT, SAT, IQ, OQ and TMV protocols. The role is onsite for about 13 billable weeks from October 2026 to January 2027, and candidates must be local or willing to relocate.
Responsabilités :
- Author and execute FAT, SAT, IQ, OQ and TMV protocols
- Test PLC logic, interlocks, alarms and recovery conditions
- Challenge sensors, actuators, vision and robotic equipment
- Review PLC programs, SCADA configurations and electrical documentation
- Document results, deviations and objective evidence
Résumé des exigences :
- Six or more years with PLC and SCADA automation equipment
- Experience in a regulated manufacturing environment
- Hands-on Rockwell and FactoryTalk View experience
- Software verification and validation lifecycle knowledge
- Strong technical writing and troubleshooting skills
Outils et compétences
Source et dates
Site carrière / système de candidatures · jazzhr
- Date publiée par l’employeur
- 2026-09-15
- Première détection par notre source
- 2026-10-09
- Mise à jour du dossier source
- 2026-10-16
Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.
Détails du poste
| Niveau | Senior |
| Domaine | Développement logiciel |
| Expérience | 6 an(s) et plus |
| Heures par semaine | 40 (estimé) |
| Déplacements | avion : aucun · route : aucun |
| Milieu de travail | Usine, Laboratoire |
| Position | Assis et debout |
| Exigences physiques | physique faible · ordinateur élevé |
| Langues | English |
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…
| Champ | Valeur |
|---|---|
| Secteur | Biotechnology |
| Taille | 51-200 employees |
| Siège social | San Diego, California |
| Type d’organisation | Privately Held |
| Fondée en | 1996 |
| Spécialités | Computer ValidationCommissioning & Qualification (C&Q)Cleaning & Process ValidationProject ManagementAutomation & Control SystemsIT ServicesCalibrationProcess Equipment & Facility QualificationQuality & Regulatory Servicesand Temperature Mapping |
| Offres sur Jobsy | 1 |
| Voir la page |
Location: Cambridge, Ontario, Canada — onsite
Engagement: Contract, with possibility of extension
Anticipated term: October 19, 2026 through January 2027
Duration: Approximately 13 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 industrial controls, automation architecture, 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
- Author, review, and execute FAT, SAT, IQ, OQ, and Test Method Validation protocols.
- 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 programs, SCADA configurations, automation architecture, control narratives, 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.
- Experience in a regulated manufacturing environment.
- Demonstrated expertise authoring and executing FAT, SAT, IQ, OQ, and TMV protocols.
- Strong understanding of the software verification and validation lifecycle.
- Advanced knowledge of PLC programming concepts and industrial automation architecture.
- Hands-on experience 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.
How to Apply
Please submit a résumé highlighting your experience with:
- Medical-device or regulated automated assembly equipment
- Rockwell PLCs, FactoryTalk View, and Ignition
- FAT, SAT, IQ, OQ, and TMV execution
- Software verification and validation
- Robotics, vision systems, and industrial controls
- Databases, data integrity, and part traceability
Journal
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