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Market research interviewer Jobs in Pointe-Claire, QC

Last updated: 2 days ago
  • Promoted
Pre-Market Regulatory Affairs Specialist

Pre-Market Regulatory Affairs Specialist

Cameleon RHPointe-Claire, QC, ca
Full-time +1
Spécialiste, Affaires Réglementaires Pré-Commercialisation.Chez Caméléon RH, nous croyons au bonheur au travail et ceci passe essentiellement par un bon jumelage entre le bon rôle, la bonne entrepr...Show moreLast updated: 7 days ago
Senior CRA / Clinical Research Associate- FSP

Senior CRA / Clinical Research Associate- FSP

ParexelRemote, Quebec, Canada
Remote
When our values align, there's no limit to what we can achieve.Parexel FSP is looking for a CRA in the Ontario and Quebec Area of Canada. Cell Therapy Trial experience strongly preferred.The Clinica...Show moreLast updated: 30+ days ago
Sr. Director, Biopharma Supplier Strategy & Market Intelligence

Sr. Director, Biopharma Supplier Strategy & Market Intelligence

MCD McKesson Canada Corporation / La Corporation McKesson Canada4705 Dobrin Street, CAN, QC, Laurent, Saint
CA$132,200.00–CA$220,300.00 yearly
Full-time
Le directeur ou la directrice principal(e), stratégie fabricants et information commerciale chez McKesson Canada est responsable d’élaborer la stratégie globale pour les fabricants biopharmaceutiqu...Show moreLast updated: 11 days ago
Responsible analyst, market trends and customers insights (3 positions)

Responsible analyst, market trends and customers insights (3 positions)

MICHELINLaval
CA$107,600.00 yearly
Full-time
Responsible analyst, market trends and customers insights (3 positions).Michelin, the Worldwide leader in Tires, is hiring!. We have 3 positions available, including two intermediate roles and one s...Show moreLast updated: 30+ days ago
Market Access Manager

Market Access Manager

ServierLaval, Québec, CA, HTS
Permanent
Servier Canada, with its main office located in Laval, Quebec is a subsidiary of the Servier Research Group, a private international pharmaceutical company governed by a foundation, with its headqu...Show moreLast updated: 6 days ago
Research Advisor

Research Advisor

Cuso InternationalLaval, QC, CA
Full-time
This Volunteer Placement is Located in : .Please submit a Spanish Resume and Statement of Interest.Eligibility : Open to Canadian Citizens and Permanent Residents of Canada only.This is your opportuni...Show moreLast updated: 30+ days ago
Sr. Market Intelligence Analyst

Sr. Market Intelligence Analyst

Bausch & LombLaval, Canada
CA$36,000.00 yearly
Conduct sales performance and market analysis, evaluate, and interpret data trends, propose business cases, and financial justification to support the forecast and business development process.Work...Show moreLast updated: 30+ days ago
Research Assistant, R&D

Research Assistant, R&D

CIRION BioPharma ResearchLaval, Canada
CA$47,320.00–CA$87,887.80 yearly
Description Research Assistant, R&D (RH2024-003)Location : Laval, Canada CIRION BioPharma Research is looking for a Research Assistant. Under the supervision of the Director, Research and Development...Show moreLast updated: 30+ days ago
  • Promoted
Chemist - Analytical Research and Development

Chemist - Analytical Research and Development

Minakem MontrealLaSalle, Quebec, Canada
Permanent
Description du poste : Relevant du Gestionnaire, Recherche et Développement, vos principales fonctions seront de rédiger des spécifications et méthodes analytiques, effectuer des validations de méth...Show moreLast updated: 5 days ago
Director and Assistant Market Leader, BMO Private Wealth

Director and Assistant Market Leader, BMO Private Wealth

BMOLaval, QC
CA$68,000.00–CA$126,000.00 yearly
Part-time
Supports the organization's growth objectives by enhancing profitability, market share and loyalty of the assigned branch / market with a focus on recruitment, operational and sales compliance, and...Show moreLast updated: 30+ days ago
Demand Planner - US Major Retail Market

Demand Planner - US Major Retail Market

Services de Gestion Quantum LtéeMontréal / Saint Laurent, Quebec, Canada
Permanent
Position : Demand Planner - US Major Retail MarketLocation : Saint-LaurentOur client is seeking a Demand Planner to join their team in Saint-Laurent. Main Responsibilities : - Facilitate collaborative p...Show moreLast updated: 19 days ago
  • Promoted
Customer Service Part Time Computer Work from Home Job

Customer Service Part Time Computer Work from Home Job

EA SolutionsLaval, Qc
CA$34.00 hourly
Remote
Customer Service Part Time Computer Work from Home Job.Work from Home Administration - Computer Online Data Entry & Short Studies / Feedback - Part Time & Full Time Work - No Experience Neede...Show moreLast updated: 30+ days ago
Remote Market Research Panel - Call Center Agent Welcome - No Experience

Remote Market Research Panel - Call Center Agent Welcome - No Experience

Apex Focus GroupLaval, Quebec, Canada
CA$850.00 weekly
Remote
Position : Remote Market Research Panel - Call Center Agent Welcome (Part Time / Full Time) - No ExperienceOur company is looking for qualified candidates to take part in paid national and local foc...Show moreLast updated: 30+ days ago
  • Promoted
Research Analyst - Urban Planning

Research Analyst - Urban Planning

City of Pointe-ClairePointe-Claire, Quebec, Canada
Full-time
Department mission Plan and oversee urban planning to ensure citizens have a quality of life focused on environmental, social, cultural and economic sustainability. Responsibilities and goals Report...Show moreLast updated: 2 days ago
  • Promoted
Remote Work – No Experience – Product Tester

Remote Work – No Experience – Product Tester

OCPAChâteauguay, Quebec, CA
CA$45.00 hourly
Remote
Product Testers are wanted to work from home nationwide in the US to fulfill upcoming contracts with national and international companies. We guarantee 15-25 hours per week with an hourly pay of bet...Show moreLast updated: 30+ days ago
Oncology Clinical Research Associate - Canada -

Oncology Clinical Research Associate - Canada -

ScimegaLaval, Quebec
CA$46,147.00 yearly
Under the direction of the Director, Clinical and Scientific Affairs, the CTL is responsible for execution of clinical trials, from the site selection, start-up and enrollment phases up to the stud...Show moreLast updated: 30+ days ago
  • Promoted
Executive Assistant

Executive Assistant

Groupe ParimaLaval, Quebec
Quick Apply
Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO), established in 1994.For over 25 years, we have developed expertise in the development and manufacturing of non-sterile...Show moreLast updated: 30+ days ago
Product Manager

Product Manager

PelicanLaval, Quebec
CA$53.85 hourly
The Product Manager is responsible for carrying out marketing research, managing and executing nautical product plans focused on consumer segments and mass retailer needs. He / she must build personas...Show moreLast updated: 30+ days ago
Pre-Market Regulatory Affairs Specialist

Pre-Market Regulatory Affairs Specialist

Cameleon RHPointe-Claire, QC, ca
7 days ago
Job type
  • Full-time
  • Permanent
Job description

English is below

Spécialiste, Affaires Réglementaires Pré-Commercialisation

Chez Caméléon RH, nous croyons au bonheur au travail et ceci passe essentiellement par un bon jumelage entre le bon rôle, la bonne entreprise, le bon patron et l’environnement qui sera stimulant pour vous! Nous sommes là pour vous écouter, vous comprendre et connaître la personne derrière le curriculum vitae. Nous nous engageons à vous présenter des offres qui vous permettront de vous épanouir et de vous réaliser en tant que professionnel, mais aussi en tant qu’individu.

Êtes-vous prêt pour l’aventure Caméléon? Notre expertise, vos couleurs!

Location  :   Pointe-Claire.

Type d’emploi  :    Le poste est permanent temps plein.

Ton environnement de travail  :

À la recherche d'une opportunité dans une grande entreprise où l'environnement de travail est rapide, dans laquelle de grands projets se trament?

Ton quotidien, en quelques lignes :

En tant que Spécialiste des affaires réglementaires avant commercialisation, vous contribuerez au succès des nouvelles offres de produits en développant / exécutant la stratégie réglementaire et les plans tactiques réglementaires tout au long du processus de conception et de développement, ainsi qu'en assurant l'enregistrement des nouveaux produits dans les délais et avec succès.

Votre participation active à des équipes interfonctionnelles ainsi que le développement d'une relation de travail étroite avec les autorités sanitaires (États-Unis, Canada, Europe) et les parties prenantes internes seront essentiels à votre réussite.

  • Élaborer et mettre en œuvre la stratégie et les plans tactiques en matière de réglementation avant la mise en marché;
  • Fournir des informations réglementaires stratégiques tout au long du processus de contrôle de la conception des dispositifs médicaux;
  • Préparer le dossier technique / les résumés du dossier technique pour les nouveaux produits conformément aux exigences des États-Unis, du Canada et de l'Europe;
  • Communiquer rapidement aux parties prenantes internes tout risque lié aux produits ainsi que toute modification de la réglementation concernant les nouveaux produits ou les offres d'extension de gamme;
  • Participer à des projets d'amélioration des processus et des outils;
  • Contribuer à la création de spécifications techniques de production et de documents techniques contrôlés similaires / liés aux produits.

La petite liste des indispensables   :

  • Licence en ingénierie, sciences de la vie, qualité / réglementation ou discipline technique connexe;
  • Au moins deux ans d'expérience en affaires réglementaires dans un environnement BPF (bonnes pratiques de fabrication), de préférence dans le domaine des dispositifs médicaux;
  • Connaissance des exigences réglementaires applicables aux dispositifs médicaux (objectif principal), aux produits de santé naturels et aux médicaments (Canada, États-Unis et Europe) et expérience à travailler avec les agences de réglementation;
  • Expérience en gestion de projets et en coordination de multiples tâches et projets parallèles dans des délais définis et / ou serrés;
  • Bilinguisme (français et anglais);
  • Compétences stratégiques, esprit critique fondé sur le risque, compétences analytiques et approche axée sur les résultats;
  • Solides compétences en matière de communication et capacité à interagir et à influencer.
  • Bonnes raisons pour postuler   :

  • Rémunération compétitive assortie d'un régime de pension;
  • Vous rejoindrez une équipe dynamique et diversifiée où votre impact sur la perception de l'entreprise sera valorisé et où vous pourrez contribuer au développement individuel et à la succession au sein de l'organisation.
  • Pre-Market Regulatory Affairs Specialist

    At Caméléon RH, we believe in happiness at work, and that means matching the right role with the right company, the right boss and the right environment to keep you energized! We're here to listen, understand and get to know the person behind the resume. We're committed to presenting you with offers that will enable you to grow and realize your full potential, not only as a professional, but also as an individual. Are you ready for the Caméléon adventure?

    Location :  Pointe-Claire.

    Type of

    position :   Permanent and full time.

    Your work environment

    Are you looking for an opportunity in a large company where the work environment is fast-paced and there are major projects in the works?

    Your day-to-day :

    As Pre-Market Regulatory Affairs specialist you will contribute to the success of new product offerings by developing / executing the regulatory strategy and regulatory tactical plans throughout the design and development process as well as by ensuring the timely and successful registration of new products.

    Your active participation in cross-functional teams as well as developing a close work relationship with health authorities (US, Canada, Europe) and internal stakeholders will be critical to your success.

  • Develop and execute the pre-market regulatory strategy and tactical plans;
  • Provide strategic regulatory input throughout the design control process of medical devices;
  • Prepare the technical file / technical file summaries for the new products as per US, Canada and European requirements;
  • Communicate promptly to internal stakeholders any product-related risks as well as any changes in regulations with respect to new product or line-extension offerings;
  • Participate in projects involving process improvements / tools;
  • Support the creation of technical production specifications and similar / related controlled technical product documentation.
  • A short list of essentials :

  • Bachelor’s degree in engineering, life sciences, quality / regulatory or related technical discipline;
  • Minimum of 2 years experience in Regulatory Affairs in a GMP (Good Manufacturing Practices) environment, preferably in medical devices;
  • Knowledge of regulatory requirements for medical devices (primary focus), natural health products and drug products (Canada, US and Europe) and experience in dealing with regulatory agencies;
  • Experience in project management and coordination of multiple parallel tasks and projects within defined and / or tight timelines;
  • Bilingualism (French and English);
  • Strategic skills, risk-based critical thinking, and analytical skills and a results-driven approach;
  • Strong communication skills with the ability to interact and influence.
  • Good reasons to apply :

  • Competitive compensation with pension plan;
  • You'll join a dynamic and diverse team where your impact on the company's perception will be valued, and where you can contribute to individual development and succession within the organization.