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Specialist/Project Manager, regulatory affairs
- QC, Canada
Full-time · Temporary
This opening has closed.
The original listing is kept below for reference.
Job details
- Job type
- Full-time · Temporary
- Posting language
- English
- Posted
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Search current openingsOriginal job description
Archived listing. The details below describe a past opening.
Brief description of the position :
In order to meet the needs of its clients in the Cosmetic sector, FOP CONSULTANTS is looking for regulatory affairs consultants to carry out various mandates. The main missions would be to support all 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 pharmaceutical regulation.
Main responsibilities :
Without limitation, the main tasks involve:
- Manage project related to the pharmaceutical 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 science (chemistry, biochemistry, biology, pharmaceutical, pharmacovigilance, etc.), or any other related discipline;
- 1 (one) to 10 (ten) years of industry experience, preferably in the (bio)pharmaceutical sector;
- Project management (an asset);
- Experience in regulatory affairs in the pharmaceutical field;
- Knowledge of regulations (Health Canada, FDA, EMA);
- Excellent skills in MS Office Suite;
- Good communication and writing skills in French and English;
- Mobility (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.
More about this job
Responsibilities
The Regulatory Affairs Specialist at FOP Consultants will manage regulatory projects, prepare documents for health authorities, and keep teams informed about regulatory changes. The role also writes procedures and trains staff.
Requirements
Candidates need a science-related degree, one to ten years of industry experience (preferably in biopharmaceuticals), and knowledge of Health Canada, FDA and EMA regulations. Fluent French and English writing skills and MS Office are required.
Skills
- Regulatory submissions
- Health Canada regulations
- FDA regulations
- EMA regulations
- SOP writing
- Regulatory surveillance
- Project management
- Technical writing
- Staff training
- MS Word
- MS Excel
- MS PowerPoint
- Bilingual French and English communication
- Risk assessment
- Non-conformity management
Benefits
- Group insurance
- Professional insurance
- Vacations: 3 weeks
- Paid sick leave: 3 days
- Monthly transportation fees
- Career advancement opportunity
- Continuing education
Categories
- Consulting
- Healthcare
- Science & Research
Keywords
- Regulatory affairs
- Pharmaceutical regulation
- Health Canada
- FDA
- EMA
- Regulatory submissions
- SOP writing
- Regulatory surveillance
- Cosmetic regulation
- Project management
- Regulatory consultant
- Compliance
- Pharmacovigilance
- Bilingual French English
- MS Office
- Biopharmaceutical
Seniority
Mid level
Perks
- Generous paid time off
- Transit support
Tools
- MS Office
Languages
- English
- French
Fields of study
- Chemistry
- Biochemistry
- Biology
- Pharmaceutical sciences
- Pharmacovigilance