Publié il y a 19 jours
CQV ENGINEER
@ EFOR
Ontario
En bref
EFOR is hiring CQV Engineer Consultants for pharma and biotech projects in the Greater Toronto Area, all levels welcome. The work covers commissioning, qualification and validation, including writing and executing IQ/OQ/PQ protocols with regulatory compliance. The role is full-time, fully on site at client locations, and requires travel.
Responsabilités :
- Carry out commissioning, qualification and validation activities
- Write and execute IQ/OQ/PQ protocols
- Collaborate with client and project teams
- Support troubleshooting and documentation
Résumé des exigences :
- Degree in engineering, life sciences or related field
- CQV or validation experience in pharma or biotech
- Strong communication and problem-solving skills
- Available to travel and work fully on site
Source et dates
Type de source non vérifié · apify-linkedin
- Date publiée par l’employeur
- 2026-10-22
- Première détection par notre source
- 2026-11-10
- Mise à jour du dossier source
- 2026-11-10
Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.
Détails du poste
| Domaine | Assurance qualité |
| Heures par semaine | 40 (estimé) |
| Déplacements | route : modérés |
| Milieu de travail | Chez les clients, Usine |
| Position | Assis et debout |
| Exigences physiques | physique faible · ordinateur modéré |
| Langues | English |
| Formation | Baccalauréat (exigé) |
| Domaines d’études | Engineering, Life sciences |
| Avantages mentionnés | Formation payée |
Résumé et détails rédigés par l’IA à partir de l’offre; l’offre de l’employeur fait foi.
EFOR
| Champ | Valeur |
|---|---|
| Offres sur Jobsy | 1 |
CQV Engineer Consultant (Pharma) – All Levels – Fully On Site – Ontario, Canada
About US :
EFOR is an ambitious consultancy with over 3,000 consultants, specializing in the life sciences sector. 🚀
About the Role:
We are looking for CQV (Commissioning, Qualification & Validation) Engineer Consultants (all levels welcome) to join our team on projects in the Greater Toronto Area. 💊🏭
Key Responsibilities:
- Carry out commissioning, qualification, and validation activities
- Write and execute protocols (IQ/OQ/PQ) and ensure regulatory compliance
- Collaborate closely with client and project teams 🤝
- Support troubleshooting and documentation
What We’re Looking For:
- Degree in engineering, life sciences, or related field 🎓
- CQV/validation experience in pharma or biotech (all seniorities considered)
- Strong communication and problem-solving skills 💡
- Adaptable, proactive, and detail-oriented 🔍
- Available to travel and work fully on site at client locations ✈️
What We Offer:
- Training 📚
- Professional growth opportunities 📈
- Exposure to leading-edge pharma projects
- Engaged and supportive team culture 🤗
Interested? Or know someone who might be? 😊
We’re happy to receive your application or your referrals! If you know talented validation engineers who would be a great fit, please invite them to reach out, too! 😊
Journal
Visible seulement par vous. Conservé sur cet appareil, et dans votre compte une fois connecté.