Medical Device Research Development jobs
Regulatory Affairs Associate
Easily applyNutrasourceGuelph, ON- $46,563.40–$60,000.00 a year
- Full-time
- Proficient knowledge of new product and process development, current regulatory issues and regulations in Canada and the U.S. for NHPs/dietary supplements,…
Applications Scientist
Easily applyAngstrom Engineering Inc.Cambridge, ON- $25–$40 an hour
- Full-time
- Monday to Friday +2
- Flexible schedule
- Experience developing thin film deposition processes to meet pre-determined coating specifications in a research and development environment.
- DECIEMToronto, ON
- $70,000–$75,000 a year
- Contract
- Paid time off
- Employee assistance program
- Monitor detailed timelines, facilitate cross-departmental workflows, and ensure on-time delivery of key scientific milestones for active development projects.
- Integrated Resources - Hosted JobsMississauga, ON L5N 5M8
- $56.73–$63.82 an hour
- Contract
- Regulatory content may include the Clinical Dossier and/or Suite of Safety reports for drugs or medical devices.
- Pay: $ 56.73-$ 63.82/hr. on T4*.
Account Manager , Medical Communications
Easily applyOften replies in 3 daysCraft ScienceRemote- $90,000–$120,000 a year
- Full-time
- Flexible schedule
- Existing network within pharmaceutical, biotechnology, healthcare, academic research, or medical affairs organizations.
Gestionnaire – Recherche et développement
Easily applyUrgently hiringLes Aliments Lesters LimitéeLaval, QC H7S 1P7- Full-time +1
- Monday to Friday +1
- Paid time off
- Vision care
- Dental care
- Life insurance
- Employee assistance program
- Disability insurance
1 hire made in past 30 days- Chez Lesters, nous recherchons un Gestionnaire – Recherche et Développement qui sera avant tout un architecte de l’innovation et un *expert du développement…
Sr. Product Development Technician
Easily applyAgile MVMontréal, QC- Full-time +1
- Dental care
- Life insurance
- Employee assistance program
- RRSP match
- Extended health care
- Participate in the design and development of medical devices.
- Design, set up and perform tests to verify the viability and performance of medical devices.
Product Development Specialist III
Easily applyAgile MVMontréal, QC- Full-time +1
- Participate in the design and development of medical devices while following a quality system in accordance with ISO 13485.
- Job Types: Full-time, Permanent.
Product Development Specialist III
Easily applyAgile MVMontréal, QC- Full-time +1
- Participate in the design and development of medical devices while following a quality system in accordance with ISO 13485.
- Job Types: Full-time, Permanent.
Research & Development Manager (Hardware)
Easily applyCWDNiagara Falls, ON L2H 1J9- $120,000–$130,000 a year
- Full-time
- Monday to Friday
- Dental care
- RRSP match
- 7 years of experience in market research and competitive analysis.
- Oversee the development of quality control documentation and ensure effective production…
Senior Biostatistician
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $110,000–$160,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Assist in research and development of statistical methodologies and processes.
- Plan and carry out professional development activities.
Principal Biostatistician
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $150,000–$200,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Provide statistical input in protocol design and development.
- Participate in the writing of trial protocols and research proposals.
- NeuroRx ResearchMontréal, QC
- $46,624.54–$85,733.87 a year
- Full-time
- Monday to Friday
- Extended health care
- NeuroRx est un chef de file dans l'analyse avancée d'images cérébrales et la gestion de projets au service de l'industrie pharmaceutique et biotechnologique.
- Eklipse Architectural LightingMontréal, QC H1W 2M3
- Full-time
- Vision care
- Dental care
- Life insurance
- Disability insurance
- On-site gym
- Flexible schedule
- Eklipse conçoit et fabrique des solutions d’éclairage architectural premium, alliant design, innovation et exigence technique dans un environnement de…
Directeur(trice) de projets
Easily applyNewRecrutement PrécisionAlma, QC- $100,000–$120,000 a year
- Full-time +1
- Dental care
- Life insurance
- Disability insurance
- Extended health care
- Work from home
- Définir et déployer la stratégie globale des projets tout en assurant leur performance à toutes les étapes;
- Valider la documentation contractuelle et assurer…
- The Employment SolutionSaint-Eustache, QC
- Contract
- Représenter son département au sein d'un programme en développement ou d'un projet.
- Assurer la coordination et le suivi des demandes de pièces nécessaires aux…
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Job Post Details
Regulatory Affairs Associate - job post
Job details
Pay
- $46,563.40–$60,000.00 a year
Job type
- Full-time
Location
Full job description
The Regulatory Affairs Associate works in a cross-functional project environment to support assessment of products against regulatory frameworks and registration of products in North America.
Primary Responsibilities
· Compiles regulatory applications (primarily for Health Canada and the FDA) to achieve departmental and organizational objectives.
· Prepares regulatory documentation as appropriate in accordance with product classification and associated regulatory pathways (e.g., OTC/Pharmaceutical Drugs, Food Ingredients, Natural Health Products (NHPs)/Dietary Supplements, Veterinary Health Products, Cosmetics, Medical Devices).
· Supports literature reviews and drafting of safety and efficacy data.
· Supports reviews of product and manufacturing changes for compliance with applicable regulations.
· Keeps abreast of domestic and global regulatory trends, laws, and movements
Core Competencies
· Proficient knowledge of new product and process development, current regulatory issues and regulations in Canada and the U.S. for NHPs/dietary supplements, prescription and non-prescription drugs, biologics, and medical devices preferred;
· Excellent oral and written communication, including technical writing skills and the ability to review and critique regulatory documents
· Ability to work well within a team and as an individual contributor.
· Computer literacy with MS Office Suite
Qualifications
· Bachelor’s Degree in a scientific discipline
· Minimum of 1-2 years industry experience, within the regulatory affairs function of a CRO/CPG/Pharmaceutical/Nutraceutical/Medical Device company
Pay: $46,563.40-$60,000.00 per year
Work Location: In person