Mississauga, On Counselor, global regulatory compliance Jobs – 1455 Openings This Week

Regulatory Data and Content Professional (Senior Medical Writer)
Integrated Resources - Hosted Jobs —Mississauga, ON
- $56.73–$63.82 an hour
- Contract
- Google Suite
- English
- Microsoft Office
Quick apply
2d
Counselor, Global Regulatory Compliance
Fiera Capital —Toronto, ON
- $100,000–$115,000 a year
- Full-time
- Hybrid work
- Bilingual
- English
- Finance
Maintenance Licensed - Millwright
Saputo Inc. —Georgetown, ON
- $45.34–$47.73 an hour
- Overtime
- Maintenance
- English
- Analysis skills
- Paid time off
Manager, Corporate Services Sourcing
Scotiabank —Toronto, ON
- Master's degree
- Bachelor's
- Financial services
1d
Acoustic Consultant
Soft dB —Mississauga, ON
- $58,240–$93,600 a year
- Full-time
- Hybrid work
- Microsoft Excel
- English
- Microsoft Office
- Mileage reimbursement
- Life insurance
Quick apply
Senior Audit Manager, AML IB (Bilingual Spanish/English)
Scotiabank —Toronto, ON
- Bilingual
- Spanish
- Microsoft Excel
10d
Chief Agent & Head of SGL Canada
SCOR —Toronto, ON
- Hybrid work
- Leadership
Sr. Manager, Manufacturing Quality and Food Safety (QFS)
Lactalis Canada Inc —Etobicoke, ON
- $111,400–$139,200 a year
- Full-time
- Analysis skills
- Bachelor's
- In-person
- Dental care
- Tuition reimbursement
Quick apply
Level 2 or 3 Technicians
Applus+ —Burlington, ON
- Overtime
- Customer service
- Writing skills
- Microsoft Office
Shop Supervisor
VAC AERO INTERNATIONAL —Burlington, ON
- $80,000–$85,000 a year
- Full-time
- Schematics
- Customer service
- Forklift
- Disability insurance
- Dental care
Quick apply
Quality Manager
Excelitas Technologies —Mississauga, ON
- $115,000–$135,000 a year
- Full-time
- Engineering
- ERP systems
- English
Quick apply
Senior Audit Manager AML/ATF and Sanctions
Scotiabank —Toronto, ON
- Management
- Analysis skills
- Bachelor's
14d
Research and Development Solution Architect - Data Products Delivery Engine
Sanofi EU —Toronto, ON
- $105,200.00–$151,933.33 a year
- DevOps
- English
- Master's degree
Director, Business Banking Lending Acquisition & Account Management
BMO Financial —Toronto, ON
- $110,500–$192,500 a year
- Analysis skills
- Tuition reimbursement
- Life insurance
Program Administrator, Funded Programs – contract position
CWB Group - Industry Services —Toronto, ON
- $29.35–$36.00 an hour
- Bilingual
- Microsoft Word
- Microsoft Excel
- Flexible schedule
Head of Data Governance Products
Sanofi EU —Toronto, ON
- $165,800.00–$239,466.66 a year
- Azure
- Master's degree
- AWS
Branch Supervision Specialist – BPIC
BMO Financial —Toronto, ON
- $56,000–$103,500 a year
- Bilingual
- Sales
- English
- Tuition reimbursement
- Life insurance
7d
Senior Manager, Business Banking Lending Acquisition
BMO Financial —Toronto, ON
- $86,000–$160,000 a year
- Analysis skills
- Tuition reimbursement
- Life insurance
Part Time Residential Counselor (Weekends) (Toronto)
Meta Centre —Toronto, ON
- $22.56 an hour
- Part-time
- Medication administration
- Caregiving
- Associate's degree
Quick apply
Senior Manager, North American Retail Credit Operations and Compliance
BMO Financial Group —Toronto, ON
- $94,600–$176,000 a year
- Full-time
- Finance
- Analysis skills
- Project management
- Tuition reimbursement
- Life insurance

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counselor, global regulatory compliance jobs near mississauga, on

Regulatory Data and Content Professional (Senior Medical Writer)

Integrated Resources - Hosted Jobs -
Mississauga, ON

Quick apply

Job details

Contract
$56.73–$63.82 an hour
2 days ago

Qualifications

Google Suite
Project planning
English
Microsoft Office
Content development
Content strategy
Communication skills
Adobe Acrobat

Full job description

Title: Regulatory Data and Content Professional (Senior Medical Writer)
Location: Mississauga, ON Hybrid Role
Duration: 12 months+
Pay: $ 56.73-$ 63.82/hr. on T4

Work Location: This is an onsite role. Selected candidates will be required to work at the Mississauga Campus 3 days every week.

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love.

That’s what makes us Client.

The Pharma Development Regulatory (PDR) is a flexible, Product, and distinctive regulatory organization. We make decisions quickly and strategically as the environment & landscape evolves.
We innovate. Within the PDR Data and Content Chapter, we are responsible for end-to-end data interpretation, generation and execution of content strategy, insight generation to guide submission strategy, and leadership of submission planning and management for clinical projects in the Client portfolio in order to develop and maintain Client product permits/licenses to meet the needs of our patients.
We understand how data and information contribute to the strategy and quality of submissions, and thus, deliver high-quality submissions to global Health Authorities for products throughout their development lifecycle to facilitate reviews and approvals.
We ensure audit and inspection readiness and representation. Additionally, as a member of PDR, individuals understand how data and information contribute to the quality of our submissions
As a member of this Chapter, you will drive and manage data interpretation and content, including medical writing, from initiation to approval, developing data and content standards, driving and articulating key messages, content creation, strategic reuse of content, and implementing automation and next-generation systems and tools.

The Opportunity:

Leads a team of Content Strategists and/or cross-functional teams in development and execution of the content strategy for submission to global regulatory authorities in accordance with applicable regulatory guidelines/Client standards/SOPs. Regulatory content may include the Clinical Dossier and/or Suite of Safety reports for drugs or medical devices
Plans content and create timelines for the production and review of documents, ensuring alignment with overall project timelines where appropriate.
Reviews documents for organization, clarity, scientific standards, and consistency of content, data, and messaging.
Resolves issues with cross-functional contributors. Ensures compliance with regulatory requirements and internal processes
Is a key strategic participant in functional and cross functional teams and actively contributes to best practices and continuous improvement initiatives and projects
Partnering with key stakeholders, working on the molecule portfolio, or continuing to key initiatives that shape our technical, business and healthcare environments.
Maintains up-to-date knowledge of key regulatory, scientific, and medical topics relevant to drug development and disease/therapeutic areas
May act as a mentor to new or less experienced Content Strategists

Who you are:

Degree in Life Sciences or equivalent with 5 years of relevant experience in the pharmaceutical/biotechnology industry, demonstrating independent project delivery and leadership. Experience in leading cross-functional teams.
Familiar with regional/global drug and device development processes, regulations, and guidelines (e.g., GxP, GCP, ICH, ISO, and MDR/IVDR) and an understanding of GVP and GCP principles, including data integrity.
Demonstrated expertise in clinical, safety and/or device regulatory documentation throughout the product lifecycle, from early development through post-marketing activities.
Ability to independently analyze and synthesize data and non-clinical and clinical concepts from a broad range of disciplines.
Proven ability to drive outcomes in global filings (strongly preferred) and other regulatory projects by collaborating across diverse, cross-functional teams, leveraging strong communication and interpersonal skills to build trust, foster collaboration, and resolve conflicts in matrixed environments.
Excellent administrative and project planning skills, with proficiency in G Suite, Microsoft Office Suite, Adobe Acrobat, and Veeva Vault; detail-oriented, creative thinker with a curiosity to learn and adapt to change, and fluent in English (verbal and written).

Mandatory Skills Required:

Degree in Life Sciences or equivalent
5 years of relevant experience in the pharmaceutical/biotechnology industry, demonstrating independent project delivery and leadership. Experience in leading cross-functional teams.
Familiar with regional/global drug and device development processes, regulations, and guidelines (e.g., GxP, GCP, ICH, ISO, and MDR/IVDR) and an understanding of GVP and GCP principles, including data integrity.
Demonstrated expertise in clinical, safety and/or device regulatory documentation.

Top Primary Goals:

Get onboarded quickly to Client internal document development processes and relevant SOPs.
Prepare for and kick off the cross-functional authoring process for an assigned project.

#IRI-BP

Pay: $56.73-$63.82 per hour

Work Location: Hybrid remote in Mississauga, ON L5N 5M8

Quick apply

Refine Your Search

counselor, global regulatory compliance jobs in mississauga, on

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