Job Title: Regulatory Affairs Manager Location: Mississauga, Ontario (Hybrid model in a modern office) Salary Range: $100,000 - $120,000 per year, plus bonus and advantages. Work Authorization: Candidates must be legally authorized to work in Canada at the time of application and throughout employment. Visa sponsorship is not available for this role. Job PurposeAs a Regulatory Affairs Manager you will manage end-to-end regulatory activities for the assigned portfolio, shaping practical regulatory strategies that support business and consumer needs while partnering closely with internal and external stakeholders. Key ResponsibilitiesRepresent Regulatory Affairs on assigned projects, providing guidance on regulations and developing regulatory strategies. This includes review of formulas for local acceptability and claims development. Collaborate with Global and local stakeholders (commercial, global Reg, R&D; etc) to ensure regulatory contributions achieve the objectives in the strategy and achieve agreed upon standards to maximize overall project delivery time and probability of success (POS). Prepare and submit high-quality regulatory submissions for health authorities and respond effectively to health authority queries. Participate in interactions (meetings, teleconferences) with regulatory authorities to seek guidance and expedite approval of pending applications. StewardshipSupport end-to-end regulatory compliance of products in remit. Support the development of the strongest claims/advertising and promotion possible within the regulations, ensuring risks are appropriately addressed and communicated. Proactively identify potential regulatory risks and recommend solutions within defined scope of responsibility on the business. Review labelling and formulations for acceptability.



Maintain high level of knowledge on the science of products within defined portfolio. Monitor regulatory trends that could impact portfolio. Basic QualificationsMinimum of 8 years of progressive experience in Regulatory Affairs within the pharmaceutical/consumer health industry. Post-secondary degree or equivalent in Life Sciences, Pharmacy or related scientific field. Demonstrated expertise in interpreting and applying regulations and guidelines. Demonstrated ability to interface effectively with internal and external stakeholders (other commercial and technical staff, local senior management, external regulators). High ability to manage multiple complex projects and work effectively independently and as part of a cross-functional team. Preferred Qualifications5 years of experience in OTC or Consumer Health. Knowledge of submission requirements and timelines related to drugs and natural health products including NDSs, SNDSs, DINAs, PLAs. Post-graduate Regulatory Affairs Certificate/Diploma, RAC, Masters (MBA, MS, MA), or PhD/PharmD/JD. Proficiency with regulatory systems and tools (e.G. Veeva RIM, eCTD). BenefitsCompetitive compensation and annual bonus package. Comprehensive and flexible benefits program from day 1. Defined contribution pension plan with employer contribution. Optional Haleon Savings Plan with employer matching. All new parents at Haleon receive 26 weeks of fully paid leave, regardless of gender or sexuality. Inclusive, diverse, and collaborative culture. Commitment to development and career progression. Hybrid model in a modern office located in Mississauga. Fitness centre, annual fitness subsidy, and on-site bistro. Equal Opportunity EmployerHaleon is an Equal Opportunity Employer and prohibits discrimination based on any protected characteristic, ensuring all employees feel they truly belong.#J-18808-Ljbffr

📌 Regulatory Affairs Manager - C$100,000 - C$120,000 A Year (Mississauga)
🏢 Haleon
📍 Mississauga