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Added 11 mins ago
H
Principal Program Manager
HDR
Burlington, ON · Kingston, ON · Ottawa, ON · Richmond Hill, ON · Toronto, ON
- Full-time
…in people’s lives. This isn’t just a job, it's a chance to lead change, drive progress, and leave a lasting…
Added 11 mins ago
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Supervisor, Snow Removal (Seasonal)
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- Full-time
Skeena Gold + Silver Limited is a Canadian mining company with a portfolio of exploration and development projects located in northwest British Columbia, Canada. Our current focus is on the…
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- $150,000 to $200,000 CAD / year
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A supportive team environment and opportunities for professional development
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GSK

Regulatory Affairs Associate (Contract)

Mississauga, ON, Canada

Full-time

Apply About employer

Applications open in a new tab.

Job details

Job type: Full-time
Apply by: Nov 14, 2026
Posting language: English
Posted: Nov 3, 2026

Original job description

Are you a curious, collaborative scientific professional who wants to build trusted relationships with oncology clinicians and help improve patient care across Canada?

GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centred on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems.

Our diverse portfolio consists of vaccines, specialty medicines, and general medicines.

Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges.

** This is a 12-month contract, an excellent way to get your foot in the door! **

Key Responsibilities

This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:

· Provides input into the planning of submissions/activities

· Assists in the preparation of regulatory submissions/activities (i.e., NDSs, SNDSs, CTAs, NCs, Training, Compliance, etc) to aggressive targets, within a team environment

· Ensures regulatory compliance with Health Canada, industry, and GSK codes and guidelines in alignment with business needs

· Assists in the preparation of internal reports or responses to Health Canada requests

· Establishes contact and communicates with global and local teams on project related plans and issues

· Identifies and responds to issues related to assigned projects, resolves basic regulatory questions

· Communicates with and may build relationship with Health Canada

· Interprets Canadian regulations, guidelines and policies as they apply to GSK regulatory activities

· Experience working with Veeva Vault

Why you?

Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:

· B.Sc. in life science or relevant scientific field (e.g. pharmacology, toxicology, chemistry)

· Some experience in regulatory affairs

· Must possess an understanding of the Canadian Food and Drug Regulations, relevant guidelines and policies

· Must have knowledge of regulatory requirements and processes for all types of submissions

· Must have a basic understanding of drug development and commercialization process

· Agile with the ability to react quickly, provide creative solutions to problems, and navigate change

· Good oral and written communication skills

· Some demonstrated negotiation skills

· Accountable to simultaneously work on multiple projects and to meet tight timelines

· Excellent attention to detail and accuracy of work

· Acts with integrity and demonstrates a strong quality mindset

· Ability to provide and receive feedback, raise issues, share experiences and lessons learned

· Proactive and seeks to constantly learn and develop. Ensures that skills meet changing business needs

· Collaborative with the ability to work with diverse groups of individuals in a team and to express opinions, including as part of group discussions. Open to diverse ideas, styles and perspectives

· Competence with electronic business environment and computer skills including Word, Excel, PowerPoint, Outlook

Preferred Qualifications:
If you have the following characteristics, it would be a plus:

· Graduate degree and/or Post-Graduate Certificate in Regulatory Affairs.

Working Model

This role is based in Canada and is hybrid out of our Mississauga location. You will combine on-site collaboration with flexible remote work.

Ready to apply?
We welcome applications from people who bring scientific curiosity, collaboration and a patient-centered mindset. If this role aligns with your experience and purpose, please apply now. We look forward to learning how you can help get ahead of disease together.

Skills

Agile Planning, Business Acumen, Change Management, Digital Fluency, Learning Agility, Problem Solving, Regulatory StrategiesIn compliance with Ontario's provincial pay transparency legislation, this job posting includes a salary range to support equitable and informed hiring practices. The annual compensation for this role is CAD82,000 to CAD132,000 , determined based on experience, qualifications, and internal equity. GSK is dedicated to promoting transparency and fairness throughout our recruitment process.Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process.

Why GSK?
Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. GSK is committed to accommodating persons with disabilities. If you need accommodation at any stage of the application process or want more information on our accommodation policies, please contact us at canada-recruitment@gsk.com. Please do not send resumes to this e-mail and instead apply through the online application process of this posting.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

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More about this job

Responsibilities

The role involves planning and preparing regulatory submissions such as NDSs, SNDSs, and CTAs while ensuring compliance with Health Canada guidelines. You will also communicate with global and local teams to resolve regulatory issues and support project-related activities.

Requirements

Candidates must hold a B.Sc. in a life science field and possess experience in regulatory affairs with an understanding of Canadian Food and Drug Regulations. Strong communication, negotiation, and project management skills are required to navigate complex regulatory environments and meet tight deadlines.

Skills

Regulatory Affairs
Health Canada Compliance
Veeva Vault
Regulatory Submissions
Drug Development
Commercialization Process
Negotiation
Project Management
Communication
Attention To Detail
Agile Methodology
Problem Solving
Change Management
Business Acumen
Digital Fluency
Learning Agility

Visa sponsorship

Not detected in the job text

Keywords

Regulatory Affairs
Oncology
Health Canada
NDS
SNDS
CTA
Veeva Vault
Drug Development
Compliance
Pharmacology
Toxicology
Chemistry
Life Science
Regulatory Submissions
Project Management
Hybrid Work
Biopharma
Vaccines
Specialty Medicines
Regulatory Guidelines

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