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Jubilant Pharma Limited

Gestionnaire de projets, Transferts technologiques / Project Manager, Technology Transfers

Montreal, QC, Canada

Job type: Full-time
Apply by: Oct 30, 2026
Posting language: English · French
Posted: Sep 30, 2026

Apply About employer

Applications open in a new tab.

Original job description

English section of this bilingual listing.

At Jubilant Radiopharma, we help healthcare professionals deliver essential patient care through high-quality nuclear medicine products. We value collaboration, innovation, and respect for people. We are committed to creating an inclusive workplace where everyone can contribute, learn, and grow.

Role Overview

As Project Manager, Technology Transfers, you will lead technology transfer projects from planning through implementation. Working closely with customers and cross-functional teams, you will help ensure products, processes, documentation, and operational readiness activities are successfully transferred to receiving sites while meeting quality, regulatory, budget, and timeline requirements.

12-month contract

Key Responsibilities

Lead technology transfer projects for PET and SPECT radiopharmaceutical products across the network.
Serve as the primary customer contact and manage project scope, timelines, risks, and deliverables.
Coordinate cross-functional teams including Operations, Manufacturing, Quality, Supply Chain, Commercial, and Business Development.
Ensure readiness of batch records, SOPs, validation protocols, analytical methods, and all required documentation.
Facilitate project meetings, customer updates, and leadership reviews.
Support business development activities through feasibility assessments and site capability evaluations.
Ensure projects are executed in compliance with FDA regulations, cGMP requirements, and company quality standards.
Build strong partnerships with stakeholders to support smooth transitions and successful technology transfer execution.

Qualifications

Bachelor’s degree in Life Sciences, Pharmacy, Engineering, or a related field.
Minimum of five (5) years of project management experience in the pharmaceutical, biotech, or radiopharmaceutical industry.
Experience with technology transfer, process validation, manufacturing scale-up, or related activities.
Experience working in cGMP-regulated manufacturing environments.
Strong understanding of FDA regulations, FDA 211/212 requirements, and quality systems.
Demonstrated ability to manage complex, multi-site projects and collaborate across diverse stakeholder groups.
Strong communication, organization, and problem-solving skills.
Excellent communication skills in both French and English as the incumbent must regularly communicate and collaborate with regulatory agencies and business stakeholders outside Quebec.
PMP certification preferred.
Experience in PET/SPECT radiopharmaceuticals, nuclear medicine, or specialty pharmaceutical manufacturing preferred.
Willingness to travel in support of project execution and technology transfer activities.

Read the full bilingual original

À propos de Jubilant Radiopharma

Chez Jubilant Radiopharma, nous aidons les professionnels de la santé à offrir des soins essentiels aux patients grâce à des produits de médecine nucléaire de haute qualité. Nous croyons à la collaboration, à l’innovation et au respect des personnes. Nous sommes engagés à créer un milieu de travail inclusif où chacun peut contribuer, apprendre et réussir.

Aperçu du poste

À titre de Gestionnaire de projets, Transferts technologiques, vous dirigerez des projets de transferts technologiques de la planification à la mise en ?uvre. En collaboration avec des clients et des équipes multidisciplinaires, vous veillerez au transfert réussi des produits, procédés, documents et activités de préparation opérationnelle vers les sites récepteurs, tout en respectant les exigences de qualité, de conformité réglementaire, de budget et d’échéancier.

Contrat temporaire de 12 mois

Responsabilités principales

Diriger des projets de transfert technologique pour des produits radiopharmaceutiques PET et SPECT à travers le réseau.
Agir comme principal point de contact pour les clients et gérer la portée des projets, les échéanciers, les risques et les livrables.
Coordonner les équipes interfonctionnelles, notamment les Opérations, la Fabrication, l’Assurance qualité, la Chaîne d’approvisionnement, les équipes Commerciales et le Développement des affaires.
Veiller à la préparation et à la disponibilité des dossiers de lot, des procédures opératoires normalisées (SOP), des protocoles de validation, des méthodes analytiques et de toute autre documentation requise.
Animer les réunions de projet, fournir des mises à jour aux clients et présenter l’avancement aux équipes de direction.
Soutenir les activités de développement des affaires grâce à des évaluations de faisabilité et des analyses des capacités des sites.
Assurer l’exécution des projets conformément aux réglementations de la FDA, aux exigences des BPF (cGMP) ainsi qu’aux normes de qualité de l’entreprise.
Collaborer efficacement avec les parties prenantes afin d’assurer une transition harmonieuse et une mise en ?uvre réussie des transferts technologiques.

Qualifications

Baccalauréat en sciences de la vie, en pharmacie, en génie ou dans un domaine connexe.
Minimum de cinq (5) ans d’expérience en gestion de projets dans les secteurs pharmaceutique, biotechnologique ou radiopharmaceutique.
Expérience en transfert technologique, validation de procédés, augmentation d’échelle de fabrication ou dans des activités connexes.
Expérience dans un environnement de fabrication réglementé selon les exigences cGMP.
Excellente compréhension des réglementations de la FDA, des exigences FDA 211/212 et des systèmes qualité.
Capacité démontrée à gérer des projets complexes impliquant plusieurs sites et à collaborer avec divers groupes de parties prenantes.
Excellentes aptitudes en communication, en organisation et en résolution de problèmes.
Excellentes habiletés de communication en français et en anglais puisque la personne titulaire doit communiquer et collaborer de façon régulière avec des agences réglementaires et des intervenants d’affaires situés à l’extérieur du Québec.
Certification PMP, un atout.
Expérience dans le domaine des radiopharmaceutiques PET/SPECT, de la médecine nucléaire ou de la fabrication pharmaceutique spécialisée, un atout.
Disponibilité pour voyager afin de soutenir l’exécution des projets et les activités de transfert technologique.

ENGLISH

Project Manager, Technology Transfers

About Jubilant Radiopharma

Role Overview

12-month contract

Key Responsibilities

Lead technology transfer projects for PET and SPECT radiopharmaceutical products across the network.
Serve as the primary customer contact and manage project scope, timelines, risks, and deliverables.
Coordinate cross-functional teams including Operations, Manufacturing, Quality, Supply Chain, Commercial, and Business Development.
Ensure readiness of batch records, SOPs, validation protocols, analytical methods, and all required documentation.
Facilitate project meetings, customer updates, and leadership reviews.
Support business development activities through feasibility assessments and site capability evaluations.
Ensure projects are executed in compliance with FDA regulations, cGMP requirements, and company quality standards.
Build strong partnerships with stakeholders to support smooth transitions and successful technology transfer execution.

Qualifications

Bachelor’s degree in Life Sciences, Pharmacy, Engineering, or a related field.
Minimum of five (5) years of project management experience in the pharmaceutical, biotech, or radiopharmaceutical industry.
Experience with technology transfer, process validation, manufacturing scale-up, or related activities.
Experience working in cGMP-regulated manufacturing environments.
Strong understanding of FDA regulations, FDA 211/212 requirements, and quality systems.
Demonstrated ability to manage complex, multi-site projects and collaborate across diverse stakeholder groups.
Strong communication, organization, and problem-solving skills.
Excellent communication skills in both French and English as the incumbent must regularly communicate and collaborate with regulatory agencies and business stakeholders outside Quebec.
PMP certification preferred.
Experience in PET/SPECT radiopharmaceuticals, nuclear medicine, or specialty pharmaceutical manufacturing preferred.
Willingness to travel in support of project execution and technology transfer activities.

Apply About employer

More about this job

Responsibilities

Lead PET and SPECT radiopharmaceutical technology transfer projects from planning through implementation, managing customer relationships, scope, timelines, risks, and deliverables. Coordinate cross-functional teams and required documentation, support feasibility assessments, and ensure transfers meet FDA, cGMP, quality, budget, and schedule requirements.

Requirements

Requires a bachelor’s degree in life sciences, pharmacy, engineering, or a related field, and at least five years of project management experience in pharmaceutical, biotechnology, or radiopharmaceutical settings. Candidates need experience with technology transfer or related manufacturing activities, cGMP and FDA requirements, strong communication and organizational skills, fluency in French and English, and willingness to travel; PMP certification and PET/SPECT experience are preferred.

Skills

Project Management
Technology Transfer
Cross-Functional Coordination
Project Scope Management
Timeline Management
Risk Management
Regulatory Compliance
cGMP
FDA Regulations
Process Validation
Manufacturing Scale-Up
Quality Systems
Feasibility Assessment
Site Capability Evaluation
French-English Communication

Visa sponsorship

Not detected in the job text

Keywords

Technology Transfer
PET Radiopharmaceuticals
SPECT Radiopharmaceuticals
Nuclear Medicine
Project Management
Cross-Functional Teams
Project Scope
Project Timelines
Risk Management
Project Deliverables
Batch Records
Standard Operating Procedures
Validation Protocols
Analytical Methods
Operational Readiness
Feasibility Assessments
Site Capability Evaluations
FDA Regulations
FDA 21 CFR Parts 211 And 212
cGMP
Quality Systems
Process Validation
Manufacturing Scale-Up
PMP Certification
Pharmaceutical Manufacturing
Business Development
French
English
Multi-Site Projects
Customer Communication

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