Medical Device Regulatory Affairs specialist

US Tech Solutions; Markham; On-site; CAD 60,000 - 84,000; Full time

Job summary

A leading company is seeking a Regulatory Affairs Specialist for a 6-month contract. The role involves managing regulatory submissions and change assessments for medical devices, with a hybrid work schedule. Candidates should have a Bachelor’s degree and 2-5 years of relevant experience.

Qualifications

• A minimum of 2-5 years of experience in regulatory affairs.
• Preferred experience with medical devices.

Responsibilities

• Support/manage regulatory change assessments and submissions to Health Canada.
• Manage documentation and system updates as required.

Skills

Excellent communication

Proficiency with Microsoft Excel

Collaborative and openness

Education

Bachelor’s Degree

Job description

Duration: 6 months contract

Job Description:

• Support/manage medical device regulatory change assessments and regulatory submissions to Health Canada, system updates, managing documentation and other duties
• Hybrid work schedule (3 days onsite and 2 days remote – Mandatory no negotiation)

Responsibilities:

• Excellent communication and comprehension of the English language
• Proficiency with Microsoft Excel and general computer skills
• Collaborative and openness

Experience:

• A minimum of 2-5 Years of experience

Skills:

• previous regulatory affairs experience is preferred,
• Especially experience with Medical devices

Education:

• A minimum of a Bachelor’s Degree is required

About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com.

US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,
national origin, disability, or status as a protected veteran

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