Specialist/Project Manager, regulatory affairs

3 weeks ago


Québec QC, Canada Fopconsultants Full time

Brief description of the position :

In order to meet the needs of our customers in the Medical Devices sector, we are looking for regulatory affairs consultants to carry out various mandates. The main missions would be to support all of the different departments in their regulatory requirements process, participate in staff training regarding regulatory instructions, write documents for the regulations authorities and collaborate on any project involved in medical device regulation.

Main responsibilities:

Without limitation, the main tasks involve:

  • Manage project related to the medical device regulations;
  • Review and write documents for the submission of the regulation’s authorities;
  • Ensure regulatory section is taken into account in every aspect of a project;
  • Proceed to regulatory surveillance to be aware of any changing in order to reduce non conformity risks;
  • Write the standard operating procedures (SOPs) related to regulations;
  • Train or participate to the training of the personnel in charge of regulatory process;
  • Support by your technical expertise the less experienced personnel;
  • Participate to the weekly or monthly meetings about the regulatory cases;
  • Provide solutions to problems encountered and perform all tasks relevant to the mandate;
Qualifications:
  • Bachelor’s or Master’s degree in sciences (Medical Technology, Chemistry, Biochemistry, Pharmacology, etc), in biomedical engineering or any other related discipline;
  • 1 (one) to 10 (ten) years of experience in medical device or pharmaceutical industries;
  • Strong project management skills (an asset);
  • Experience in regulatory affairs in medical device or pharmaceutical industries (an asset);
  • Proven knowledge of ISO 13485 Regulation;
  • Proven knowledge of the medical device classes: I, IIa, IIb et III;
  • Proven knowledge of Health Canada and FDA Regulations;
  • Writing/oral communication skills, English and French;
  • Perfect bilingualism (an asset);
  • Valid class 5 driver’s license (an asset);
  • Mobility, willing to travel (an asset).
Personal skills:
  • Leadership;
  • Rigor et discipline;
  • (Organize), able to manage several projects;
  • Analytical and critical mindset;
  • Perseverance;
  • Humility.
What we offer :

In order to allow the full development of our team members, FOP CONSULTANTS guarantee the support and comfort necessary for the achievement of their mandate. The main advantages offered are as follows:

  • Competitive wages;
  • Group insurance;
  • Professional insurance;
  • Remote work, according to the customer needs;
  • Vacations: 3 weeks;
  • Paid sick leave: 3 days;
  • Monthly transportation fees;
  • Career advancement opportunity;
  • Continuing education.
#J-18808-Ljbffr

  • Laval, QC, Canada Bausch Health Full time

    Career Opportunities: Regulatory Affairs Specialist - CMC (11942) Requisition ID 11942 - Posted -  Canada Reg Affairs  -  R&D  -  CA - Laval  - City (1) Bausch Health Canada is the international head office of Bausch Health Companies, one of the fastest growing international pharmaceutical companies dedicated to bringing quality health and wellness...


  • Montréal, QC, Canada Lock Search Group Full time

    Regulatory Affairs Manager Montreal or Quebec City, Quebec Our client, a medical device company specializing in the production of various medical equipment and healthcare products, is in search of a Pre-Market Regulatory Affairs Manager. The incumbent will deliver the regulatory strategy and regulatory plans throughout the design and development process...


  • Montréal, QC, Canada EightSix Network Inc Full time

    Our client, a medical device company specializing in the production of various medical equipment and healthcare products, is in search of a Pre-Market Regulatory Affairs Manager. The incumbent will deliver the regulatory strategy and regulatory plans throughout the design and development process of new products. Working closely with North American and...


  • Montréal, QC, Canada Lock Search Group Full time

    Regulatory Affairs Manager Montreal or Quebec City, Quebec Our client, a medical device company specializing in the production of various medical equipment and healthcare products, is in search of a Pre-Market Regulatory Affairs Manager. The incumbent will deliver the regulatory strategy and regulatory plans throughout the design and development process...


  • Montréal, QC, Canada Lock Search Group Full time

    Regulatory Affairs Manager Montreal or Quebec City, Quebec Our client, a medical device company specializing in the production of various medical equipment and healthcare products, is in search of a Pre-Market Regulatory Affairs Manager. The incumbent will deliver the regulatory strategy and regulatory plans throughout the design and development process...


  • Montréal, QC, Canada Sagard Holdings Management Inc. Full time

    La version française est ci-dessous. Sagard is a multi-strategy alternative asset management firm active in venture capital, new venture creation, private equity, private credit, real estate, royalties with $14.5B in assets under management. Sagard also engages in private wealth management through its ecosystem partner Grayhawk. We are looking to hire a...


  • Montréal, QC, Canada Lock Search Group Full time

    Regulatory Affairs Manager Our client, a medical device company specializing in the production of various medical equipment and healthcare products, is in search of a Pre-Market Regulatory Affairs Manager. The incumbent will deliver the regulatory strategy and regulatory plans throughout the design and development process of new products. Working closely...


  • Montréal, QC, Canada Lock Search Group Full time

    Regulatory Affairs Manager Montreal or Quebec City, Quebec Our client, a medical device company specializing in the production of various medical equipment and healthcare products, is in search of a Pre-Market Regulatory Affairs Manager. The incumbent will deliver the regulatory strategy and regulatory plans throughout the design and development process...


  • Montréal, QC, Canada EightSix Network Inc Full time

    Our client, a medical device company specializing in the production of various medical equipment and healthcare products, is in search of a Pre-Market Regulatory Affairs Manager. The incumbent will deliver the regulatory strategy and regulatory plans throughout the design and development process of new products. Working closely with North American and...


  • Québec, QC, Canada Fopconsultants Full time

    Brief description of the position : In order to meet the needs of its clients in the (Bio)Pharmaceutical sector, FOP CONSULTANTS is looking for clinical trial specialist/associate consultants motivated to carry out mandates. The main missions would be to ensure the compliance of operations, materials, standards, and regulations during the execution of...


  • Gatineau, QC, Canada Borgen Project Full time

    Are you passionate about making a difference in the world? Look no further! The Borgen Project is an international organization that works at the political level to improve living conditions for people impacted by war, famine and poverty. With 20 years of experience in the advocacy space, The Borgen Project has worked to support the passage of numerous bills...


  • Brossard, QC, Canada Novo Nordisk Full time

    Novo Nordisk is a leading global healthcare company, founded in 1923 and headquartered in Denmark. REPORTS TO: Director, Ethics and Compliance # The Legal, Ethics & Compliance Department works to safeguard Novo Nordisk’s license to operate and to foster sustainable business conduct as Novo Nordisk Canada delivers life-changing therapies for the benefit of...


  • Québec, QC, Canada Fopconsultants Full time

    Brief description of the position : In order to meet the needs of its clients in the (Bio)Pharmaceutical sector, FOP CONSULTANTS is looking for pharmacovigilance consultants to carry out various mandates. The main missions would be to manage projects on adverse drug reactions, participate in the training of personnel on pharmacovigilance guidelines,...


  • Québec, QC, Canada Fopconsultants Full time

    Brief description of the position : In order to meet the needs of its clients in the (Bio)Pharmaceutical sector, FOP CONSULTANTS is looking for quality assurance consultants to carry out various mandates. The main missions would be to review and approve the quality documents (SOP, protocols, etc.), collaborate on client’s complaints, write...


  • Québec, QC, Canada Fopconsultants Full time

    Brief description of the position : In order to meet the needs of its clients in the (Bio)Pharmaceutical sector, FOP CONSULTANTS is looking for quality assurance consultants to carry out various mandates. The main missions would be to review and approve the quality documents (SOP, protocols, etc.), collaborate on client’s complaints, write...


  • Québec, Canada Colliers Project Leaders Full time

    Overview: At Colliers Project Leaders, we deliver capital project solutions to fulfill our clients’ needs across the built environment. The work we do makes a difference in communities and for the people who live there. We have a passion for it. Our commitment to realizing our clients' vision inspires us to look beyond the immediate - to the ...

  • Project Manager

    2 weeks ago


    Québec, QC, Canada CIMA Canada Inc Full time

    At CIMA+, you’ll find a place where you’ll have many opportunities to learn and develop while working on engaging projects. You will have the flexibility to manage your work on your own terms and define what work-life balance means to you. The Project Director's main role is to support our customers in carrying out projects in compliance with...


  • Québec, Canada Fivesky Full time

    Are you an experienced professional in resilience and operational continuity? Do you understand the financial sector's regulatory requirements and best practices? Can you manage projects both independently and collaboratively? Are you skilled in communication, research, and relationship-building? If you're proactive, self-motivated, thrive under pressure,...


  • Québec, Quebec, Canada Fopconsultants Full time

    Brief description of the position : In order to meet the needs of its clients in the (Bio)Pharmaceutical sector, FOP CONSULTANTS is looking for quality assurance consultants to carry out various mandates. The main missions would be to review and approve the quality documents (SOP, protocols, etc.), collaborate on client's complaints, write nonconformity,...


  • Montréal, QC, Québec, Canada Fed Manutech Full time

    Hello, I'm Marine, Recruitment and Business Development Consultant with Fed Manutech, a recruitment firm specializing in engineering and manufacturing. I work on two types of recruitment: temporary and permanent in the Greater Montreal area. Our team, experts in these fields, speak your language and work in your world.Bonjour, je suis Marine,...