5 meilleures offres (biotechnology, nepean, on) (à pourvoir)

Regulatory Affairs Project Manager
Adecco Canada —Ottawa, ON
- De 85 000 $ à 90 000 $ par an
- Temporaire
- Doctorat
- Ingénierie
- Maîtrise
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Gestionnaire d'essais cliniques II, IQVIA Biotech/Clinical Trial Manager II, IQVIA Biotech
IQVIA —Ottawa, ON
- De 116 300 $ à 193 800 $ par an
- Temps plein
- Télétravail
- Baccalauréat
- Gestion d'équipe
- Recrutement
Medical Science Liaison
Arrowhead Pharmaceuticals —Ottawa, ON
- Télétravail
- Logiciels de GRC/CRM
- Médecine
- Doctorat
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Clinical Independent Rater (CIR) – French Speaking
IQVIA —Kanata, ON
- Temps partiel
- Télétravail
- Soins infirmiers
- Médecine
- Doctorat
il y a 13 jours
Clinical Nurse
Lilium Diagnostics —Canada
- 40 $ de l’heure
- Temps plein
- Télétravail
- Soins infirmiers
- Service à la clientèle
- Expérience en laboratoire
- Assurance Dentaire
- Travail à domicile
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Gestionnaire d'essais cliniques II, IQVIA Biotech/Clinical Trial Manager II, IQVIA Biotech
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IQVIA est un fournisseur mondial de premier plan de services de recherche clinique, d'informations commerciales et de renseignements sur les soins de santé pour…
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Je souhaite recevoir la dernière alerte emploi pour les postes de ce type : biotechnology (nepean, on)

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Regulatory Affairs Project Manager

Adecco Canada -
Ottawa, ON

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Détails du poste

Temporaire | Contrat
De 85 000 $ à 90 000 $ par an

Profil recherché

Doctorat
Ingénierie
Maîtrise
Baccalauréat
Affaires
Compétences en communication

Description complète du poste

Adecco is currently hiring a Regulatory Affairs Project Manager for a contract opportunity supporting an international regulatory team in the medical device industry. This role is ideal for an experienced regulatory affairs professional with strong project management expertise and a background in In Vitro Diagnostic (IVD) medical devices. If you enjoy leading cross-functional regulatory projects, developing regulatory strategies, and ensuring compliance with global regulations, this is an excellent opportunity to contribute to the successful commercialization of innovative healthcare products.

Salary: $85,000 - $90,000 per year
Location: Ottawa, ON
Schedule: Monday to Friday, standard business hours
Employment Type: Full-time | Temporary Contract (August 2026 - December 2027)
Vacancy Status: This posting is for an existing vacancy.

Responsibilities

Lead and coordinate regulatory workstreams for IVD medical device projects, ensuring alignment with business objectives, timelines, and global regulatory requirements.
Collaborate with the International Regulatory Team to develop, document, and execute regulatory strategies supporting product development, registration, and commercialization.
Develop and maintain regulatory project plans, timelines, milestones, and deliverables.
Monitor project progress, identify regulatory risks, and implement mitigation strategies to minimize project impact.
Support regulatory activities throughout the product lifecycle, including product development, submissions, market authorization, and post-market activities.
Coordinate regulatory deliverables and support international product registrations as required.
Facilitate project meetings, provide status updates, and communicate progress to internal stakeholders.
Track regulatory milestones, project metrics, and ensure timely completion of objectives.
Support market activities and additional regulatory projects as assigned.
Ensure regulatory activities comply with applicable international regulations, including Health Canada, EU IVDR, and other global regulatory frameworks.

Qualifications

Must be legally eligible to work and reside in Canada.
Bachelor's degree in Life Sciences, Biomedical Engineering, Biotechnology, Medical Technology, Regulatory Affairs, or a related scientific discipline (Canadian or WES-verified credential required).
Advanced degree (MSc, PhD, or MBA) is considered an asset.
Minimum of 5-8 years of Regulatory Affairs experience within the medical device or IVD industry.
Minimum of 2-3 years of project management experience leading cross-functional regulatory projects.
Demonstrated experience preparing and managing IVD regulatory submissions for one or more major international markets.
Experience working within ISO 13485-compliant quality management systems.
Experience supporting products regulated under the EU IVDR (Regulation (EU) 2017/746) is strongly preferred.
Strong understanding of Health Canada Medical Devices Regulations and other global regulatory requirements.
Excellent project management, organizational, and communication skills.
Advanced proficiency with Microsoft Excel, SharePoint, and other Microsoft Office applications.
Ability to manage multiple priorities and collaborate effectively with cross-functional international teams.

Why Apply

Join an experienced international regulatory team supporting innovative medical device products.
Lead impactful regulatory projects with global market exposure.
Work in a collaborative, highly specialized healthcare environment.
Competitive compensation package.
Long-term contract opportunity with meaningful and challenging work.

Interested in this position? Apply now! Our dynamic recruitment team looks forward to helping you take the next step in your career.
At Adecco, our purpose is simple: to make the future work for everyone. We live our values - Passion, Collaboration, Inclusion, Courage, and Customer-Centricity - by fostering a workplace where diversity is celebrated and every voice matters. We encourage applications from people of all backgrounds and identities. Together, we are shaping a future that works for everyone.
If you would like to learn more about Aspire Academy to enhance your skills for your next role, feel free to ask!
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biotechnology emplois - nepean, on

Regulatory Affairs Project Manager

Gestionnaire d'essais cliniques II, IQVIA Biotech/Clinical Trial Manager II, IQVIA Biotech

Medical Science Liaison

Clinical Independent Rater (CIR) – French Speaking

Clinical Nurse

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