Fsp - Regulatory Affairs Associate

Calian CRO is looking for a Regulatory Affairs Associate on behalf of our client for a limited 12-month term contract with a possibility of renewal. The role will be primarily remote, with occasional attendance in the Montreal office for meetings. Do you have a passion for day-to-day regulatory activities? If so, we would love to hear from...

Job Summary Working within Regulatory Affairs, reporting to Head, Regulatory Affairs, Associate, Quality & Regulatory Affairs is responsible for performing the required tasks related to Regulatory Affairs. Principal Responsibilities **Regulatory Affairs**: Coordinate with the Export department the regulatory and quality documents required for product...

Job Description Summary At Paladin, we strive to offer a work environment that meets the diverse needs of our team members and advances the goals of the individual, the team and the company, while promoting flexibility, accountability and collaboration. If you're looking for a hybrid work environment, Paladin is the place for you! This position requires a...

395204BR **Regulatory Affairs Compliance Associate**: Canada **About the role** Location: Montreal, #LI-Hybrid 13 month contract About the role: We are looking for an organized, collaborative and passionate regulatory affairs professional who is driven to help us deliver our innovative treatments to patients. As a compliance lead, you will report directly...

Job Description Summary At Paladin Pharma, we strive to offer a work environment that meets the diverse needs of our team members and advances the goals of the individual, the team and the company, while promoting flexibility, accountability and collaboration. If you're looking for a hybrid work environment, Paladin is the place for you! This position...

**About us** We are professional, agile, and innovative. Our work environment includes: - Modern office setting - Food provided - Modern office setting - Growth opportunities - Wellness programs - Work-from-home days Job Summary: We are seeking a highly skilled and motivated Regulatory Affairs Specialist to join our team. As a Regulatory Affairs...

**Summary**: Location: Montreal, #LI-Hybrid About the role: The role reports to Regulatory Affairs Franchise Lead and will work with different team members. Temporary - 9 to 12 months **About the Role**: **Key Responsibilities**: - Assists in the preparation of and/or review of various regulatory submissions for new or marketed products and ensures optimal...

**See if you are our next**: **BILLINGUAL REGULATORY AFFAIRS SPECIALIST (Operating Room Experience Required)** Working at Vision Group's head office is working for the North American leader in vision correction. It means being able to concretely contribute to the development of the company and support more than 12 brands and more than 70 clinics across...

**Company Description** Ubisoft’s 19,000 team members, working across more than 30 countries around the world, are bound by a common mission to enrich players’ lives with original and memorable gaming experiences. Their commitment and talent have brought to life many acclaimed franchises such as Assassin’s Creed, Far Cry, Watch Dogs, Just Dance,...

The Regulatory Affairs Assistant is responsible for handling regulatory documents and maintaining the Investigator’s Study Files (ISFs) for all studies at the clinical research unit. **RESPONSABILITIES** More specifically, the Regulatory Affairs Assistant must: - Track the signatures of regulatory forms (i.e., QIU, FDA1572, financial disclosure forms)...

Work Term: Permanent - Work Language: English - Hours: 38 to 44 hours per week - Education: Master's degree - Experience: 5 years or more - Bioengineering and biomedical engineering - Mechanical engineering **Tasks**: - Analyze and provide advice on the managerial methods and organization of an establishment - Develop quality management and quality...

Work Term: Permanent - Work Language: English - Hours: 42 to 44 hours per week - Education: Master's degree - Experience: 5 years or more **Tasks**: - Analyze and provide advice on the managerial methods and organization of an establishment - Conduct quality audits - Develop quality management and quality assurance standards - Conduct research to determine...

Le rôle principal de l’associé(e) en réglementation - graphiste consiste à gérer la création et les révisions des maquettes pour les produits de santé animale. La personne titulaire du poste interagit directement avec les chefs de marque, des Affaires réglementaires, de l’Assurance qualité et de la Logistique. Ses fonctions administratives...

Clinical Research Manager Remote - Montreal, Quebec As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Clinical Research Manager Remote - Montreal, Quebec As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across...

Why join our team? Think you have what it takes to work in an organization where creativity, drive and ambition are valued while integrity motivates everything we do? Medicom has been in business for over 35 years, and it has kept its entrepreneurial mindset. Working with us, you will have the opportunity to get involved, have an impact, and contribute to...

Senior Legal Counsel, Paper & Packaging Location: Montreal, QC Reports to: VP, Associate General Counsel, Legal Affairs, Paper & Packaging Overview: Provide legal services and advise the Paper & Packaging Business Unit (Unit) personnel from various departments and facilities in relation to the Unit’s activities and operations in Canada & the...

Clinical Trial Coordinator - Regulatory - Hybrid - Montreal QC Fortrea is looking for problem-solvers and creative thinkers who are passionate about breaking down barriers faced by sponsors of clinical trials, and who are committed to helping transform the development process to get promising life-changing ideas and therapies to patients faster. Join us as...

Clinical Trial Coordinator - Regulatory Hybrid (50% office-based / 50% remote) - Montreal, QC As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient...