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Regulatory specialist Offres d'emploi - Quebec city qc

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Regulatory specialist • quebec city qc

Dernière mise à jour : il y a 20 heures
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Sr Regulatory Consultant

Sr Regulatory Consultant

Syneos HealthQuébec City, CA
Temps plein
Description Senior Regulatory Consultant Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, med...Voir plusDernière mise à jour : il y a 3 jours
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Conversion Specialist

Conversion Specialist

Morgan Macequébec city, qc, Canada
Temps plein
We are seeking an experienced and results-driven Conversion Rate Optimization.CRO) Strategist to lead efforts in enhancing user experiences and drive measurable. In this role, you will collaborate.C...Voir plusDernière mise à jour : il y a 20 heures
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sales specialist

sales specialist

RONASaint-Medard, CA
Temps partiel
At RONA, our employees let their passion blossom every day.Our teams are driven by the desire to help people bring their projects to life and are committed to making a difference in the communities...Voir plusDernière mise à jour : il y a 2 jours
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Digital Specialist

Digital Specialist

Robert Halflévis, qc, Canada
Temps plein
B2B digital marketing campaigns using Microsoft D365 and a full suite of marketing automation tools.This role is focused on leveraging data-driven strategies to enhance customer engagement, nurture...Voir plusDernière mise à jour : il y a 20 heures
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Training Specialist

Training Specialist

Swoonsaint-esprit, qc, Canada
40,00 $CA –48,00 $CA par heure
Temps plein
Job Title : Awareness and Training Specialist.Support development of internal security and privacy awareness campaigns including communications, videos, presentations and trainings.Facilitate produc...Voir plusDernière mise à jour : il y a 20 heures
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Regulatory and Quality Manager

Regulatory and Quality Manager

St-AmourGreater Montreal Metropolitan Area, Canada
Temps plein
Our client is a global leader in pharmaceuticals and Natural Health Products.Manager, Quality and Regulatory.Canadian subsidiary across Natural Health Products (NHPs), Drugs (DINs), and Cosmetics.H...Voir plusDernière mise à jour : il y a 9 jours
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Compliance & Regulatory Affairs Manager

Compliance & Regulatory Affairs Manager

Willson International Limitedlévis, qc, Canada
Temps plein
The Manager, Compliance & Regulatory Affairs will oversee the day-to-day operation of the Regulatory and Compliance department with a Brokerage company, while providing answers and support to clien...Voir plusDernière mise à jour : il y a 20 heures
Head of Department - Regulatory Department

Head of Department - Regulatory Department

OcéanQuébec, CA
48 000,00 $CA – 55 000,00 $CA par an
ARE YOU LOOKING TO JOIN A GREAT COMPANY WHERE YOUR CONTRIBUTION WILL BE RECOGNIZED?.READ ON, THIS OFFER IS PERFECT FOR YOU!. We are actively seeking a Head of Department – Regulatory Department who ...Voir plusDernière mise à jour : il y a plus de 30 jours
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Proposal Specialist

Proposal Specialist

Kasian Architecture Interior Design and Planningquébec city, qc, Canada
Temps plein
Our passion is strengthening connections between people and places by creating built environments that inspire and improve lives. With offices across Canada, we leverage the experience of our 250+ K...Voir plusDernière mise à jour : il y a 20 heures
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Training Specialist

Training Specialist

HyLife Foods LPquébec city, qc, Canada
CDI
HyLife is a global leader in food processing.Our vision is to be the best food company in the world.Our mission is to take care of our employees, communities, animals, and customers.We are seeking ...Voir plusDernière mise à jour : il y a 20 heures
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Sales Specialist

Sales Specialist

RONA inc.Lévis, CA
Temps plein
At RONA, our employees let their passion blossom every day.Our teams are driven by the desire to help people bring their projects to life and are committed to making a difference in the communities...Voir plusDernière mise à jour : il y a 3 jours
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Language Specialist

Language Specialist

Altis Recruitmentlévis, qc, Canada
55 000,00 $CA par an
Temps plein +1
Our client, a leading data engineering company is looking for.Multilingual Language Specialist.Full time (40 hour work week) Monday - Friday, flexible between 8am-6pm (local time zone) - hours are ...Voir plusDernière mise à jour : il y a 20 heures
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Regulatory Affairs Manager (Part-Time, Canada Based)

Regulatory Affairs Manager (Part-Time, Canada Based)

Advanced Clinicallévis, qc, Canada
Temps partiel
Advanced Clinical is a clinical development and strategic resourcing organization committed to providing a better clinical experience across the drug development journey. Our goal is to improve the ...Voir plusDernière mise à jour : il y a 20 heures
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Pharmacovigilance Specialist

Pharmacovigilance Specialist

BrunelQuebec, Canada, Canada
Temps plein
Pharmacovigilance Specialist (renewable contract)Remote – Quebec or OntarioIntroductionWe are hiring a Pharmacovigilance Specialist for one of our pharmaceutical clients based in either Ontario or ...Voir plusDernière mise à jour : il y a 9 jours
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Onboarding Specialist

Onboarding Specialist

Set 2 Closequébec city, qc, Canada
Temps plein
Set 2 Close is a premier Revenue Consulting company and HubSpot Diamond Partner, specializing in optimizing CRM solutions to enhance customer lifecycle management and revenue operations.We integrat...Voir plusDernière mise à jour : il y a 20 heures
Manager, Regulatory Affairs

Manager, Regulatory Affairs

Innomar StrategiesRemote, Quebec
151 600,00 $CA – 281 500,00 $CA par an
Télétravail
Temps plein
Our team members are at the heart of everything we do.At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on ...Voir plusDernière mise à jour : il y a plus de 30 jours
Manager, Regulatory Compliance - Gas

Manager, Regulatory Compliance - Gas

Liberty UtilitiesRawdon, Quebec,
95 000,00 $CA par an
This position may be located at any Liberty location •.This position is the owner of gas compliance maintenance plan standards and reporting, and is responsible for monitoring adherence to standards...Voir plusDernière mise à jour : il y a plus de 30 jours
Regional Manager - Montreal Centre, Quebec City and South Shore

Regional Manager - Montreal Centre, Quebec City and South Shore

EightSix NetworkQC
80 000,00 $CA – 90 000,00 $CA par an
Requisition ID : Join a purpose driven winning team, committed to results, in an inclusive and high-performing culture.Leading a team of Investment Specialists for an assigned market area, the Regio...Voir plusDernière mise à jour : il y a plus de 30 jours
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Billing Specialist

Billing Specialist

Davies Ward Phillips & Vineberg LLPlévis, qc, Canada
Temps plein
Davies is a top-tier Canadian law firm focused on high-stakes matters.With offices in Montreal, Toronto and New York, we are consistently at the centre of the most challenging deals and cases in Ca...Voir plusDernière mise à jour : il y a 20 heures
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Clinical Specialist

Clinical Specialist

Medtroniclévis, qc, Canada
Temps plein
At Medtronic, you can begin a lifelong career focused on research and innovation, championing equity and access to healthcare for all. Your leadership will make an impact, removing barriers to drive...Voir plusDernière mise à jour : il y a 20 heures
Sr Regulatory Consultant

Sr Regulatory Consultant

Syneos HealthQuébec City, CA
Il y a 3 jours
Type de contrat
  • Temps plein
Description de poste

Description Senior Regulatory Consultant Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know : WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we’re able to create a place where everyone feels like they belong. Job responsibilities Responsible for day-to-day contribution to project teams and projects. Acts as a representative of the GRAS regulatory department with other departments. Contributes technical expertise to proposals and assists with Business Development initiatives. Understands project budgets, scope of projects, allocated hours, and tracks compliance. Interacts with internal and external personnel, clients, and technical experts on projects. Conducts regulatory research on projects as needed. Provides operational advice to clients. Prepares consulting reports under guidance. Arranges, leads, and reports on client meetings. Contributes to regulatory agency meetings. Writes IND and product registration dossiers, clinical reports, and other regulatory documents for submissions. Prepares full regulatory submissions for INDs, product registrations, and post approval maintenance activities, and participates on project teams. Acts as a resource for technical knowledge. Participates in quality improvement efforts to increase overall operational efficiency. Contributes to the building of the regulatory systems and infrastructure needed for GRAS. Develops reputation for the Company as industry leader in Regulatory by attending and speaking at industry events such as seminars and association meetings, authoring articles for trade journals, and participating in industry association through memberships and on committees. Provides internal training in appropriate areas of expertise to other Departments. May act as a Line Manager to a small team, dependent on the location. Qualifications What we’re looking for BS degree, preferably in a science-related field or equivalent experience in science / regulatory / medical writing-related field. PhD preferred. Experience with preparation and approval of regulatory submissions to Health Canada Moderate regulatory, pharmaceutical / medical device related experience. Demonstrated experience in contributing to the preparation of regulatory submissions including for example IND, PMA, NDA, MAA, and CTD, including electronic submissions. Experience in niche submissions such as ODD, PIP / PMP an advantage. Excellent interpersonal / communication skills including excellent written and verbal communication skills. Excellent customer service skills, with the ability to work both as a team member and independently. Good quality management skills. Problem-solving and decision-making skills. Advanced skills in Microsoft Office Applications. Ability to interact with staff from multiple departments and offices to establish project standards. Good initiative, adaptability, and pro-activity. Strong analytical skills, good attention to detail. Ability to work concurrently on projects, each with specific instructions that may differ from project to project. Fluent in speaking, writing, and reading English. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000 Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. Additional Information : Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and / or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills / experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.