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Posted 9 days ago

Project Manager, New Product Development (Regulatory Affairs)

@ Apotex

Ontario

$96k–$134k/yr8+ years experience
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Overview

Apotex, a Canadian-based global health company, is hiring a Project Manager for New Product Development in regulatory affairs. The role leads new product submissions, deficiency responses and due diligence on partner opportunities, requiring 8+ years of pharmaceutical regulatory experience. The posting lists a salary range of $95,594.40 to $133,832.16 CAD per year and a pension plan.

Pay:

$95,594–$133,832 a year

Responsibilities:

  • Lead new product development regulatory submissions and deficiency responses
  • Assess regulatory risk of partner due diligence opportunities
  • Execute change control assessments and related database updates
  • Train and guide peers

Requirements summary:

  • B.Sc. in chemistry, biology, pharmaceutical, engineering or health sciences
  • 8+ years pharmaceutical regulatory affairs experience
  • Knowledge of Canadian and US regulatory guidelines
  • Strong leadership and communication skills
  • MS Office experience

Tools & skills

Benefits mentioned

Retirement plan
Source and dates

Employer career site / ATS feed · successfactors

Employer posting date
2026-10-29
First seen by our source
2026-10-09
Source record updated
2026-10-31

These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.

Job details

SenioritySenior
DepartmentQuality assurance
Experience8+ years
Work settingOffice
PositionMostly sitting
Physical demandsphysical low · computer high
LanguagesEnglish
Encouraged to applyPeople with disabilities
EducationBachelor’s degree (required)
Fields of studyChemistry, Biology, Pharmaceutical sciences, Engineering, Health sciences
Perks mentionedRetirement plan, Performance bonus

Summary and details written by AI from the posting; the employer’s posting is the authority.

Apotex

Saved company profile

Historical company information from a saved The Jobs API profile (LinkedIn/Crunchbase fields). It is not live-verified; figures may have changed. Missing values remain unknown.

Canadian-Based Global Health Company

Full company description

At Apotex, we are a global team empowering everyone to achieve better health. We improve everyday access to affordable, innovative medicines and health products for people around the world, with a portfolio comprising more than 550 generic, biosimilar, and innovative medicines, along with more than 225 natural health products. Headquartered in Toronto, we are the largest Canadian-based pharmaceutical company and a health partner of choice in the Americas for pharmaceutical licensing and product acquisitions. Learn more about us at www.apotex.com. To report an Adverse Reaction/Experience to Apotex, or an Apotex affiliated company, please contact: [email protected].

LinkedIn followers
295,723
People associated on LinkedIn
6,481
Reported office locations
  • 150 Signet Drive, Toronto, Ontario M9L1T9, CA
  • 50 Steinway Boulevard, Etobicoke, Ontario M9W 6Y3, CA
  • 380 Elgin Mills Road East, Richmond Hill, Ontario L4C 5H2, CA
  • 34 Spalding Drive, Brantford, Ontario N3T 6B8, CA
  • 2400 N Commerce Pkwy, Suite 400, Weston, Florida 33326, US
  • Plot No. 1 & 2, Bommasandra Industrial Area, 4th Phase, Jigani Link Road, Bangalore, Karnataka 560099, IN
  • 5th Floor, Block 'A', Building Godrej IT Park – 02 GBD, Mumbai, Maharashtra 400079, IN
Business categories
  • Emergency Medicine
  • Manufacturing
  • Pharmaceutical
Other recorded names
  • Apotex
  • Apotex Inc.
Profile identifies a recruitment agency
No
Reported total investment
8,000,000

Currency and observation date were not supplied; this is not a current valuation or a funding round.

At Apotex, we are a global team empowering everyone to achieve better health. We improve everyday access to affordable, innovative medicines and health products for people around the world, with a portfolio comprising more than 550 generic, biosimilar, and innovative medicines, along with more than 225 natural health products. Headquartered in Toronto, we are the largest Canadian-based pharmaceutical company and a…

FieldValue
IndustryPharmaceutical Manufacturing
Company size5,001-10,000 employees
HeadquartersToronto, Ontario
Organization typePrivately Held
Open jobs on Jobsy58
LinkedInView page
Job description

About Apotex Inc.

Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.

For more information visit: www.apotex.com.

Job Summary

Responsible for leading New Product Development (NPD) submission activities, including but not limited to, due diligence activities for new product opportunities, new product development submissions, and associated activities such as deficiency responses. Strong linkages need to be established with internal colleagues and development partners. Leads development of strategies and operations for projects under the NPD portfolio within GRA.

Job Responsibilities

  • Develops regulatory project strategy with appropriate risk mitigation strategies incorporated
  • Ability to recover projects that are at risk
  • Prepares/leads regulatory submissions according to current requirements, and taking into account current deficiency trends
  • Assesses potential deficiencies and works with internal/external team members to address prior to submission, or if not possible, in advance of deficiency receipt
  • Leads development of optimal deficiency response strategies with internal and external stakeholders; works with stakeholders to review/finalize responses that fully/optimally address the regulator’s deficiency questions; leads discussion with stakeholders to finalize deficiency responses by the target response date
  • Conducts thorough due diligence of opportunities brought forward by the Business Development team, and identifies all regulatory risks associated with the potential opportunity; if not provided with initial data package from the partner, requests for key elements required to conduct the thorough assessment, based on status of the development/submission for the opportunity.
  • Supports seamless product launch through timely review of change proposals, change controls, provision of documentation, and other activities as required.
  • Executes change control assessments, and any subsequent activities required as a result of the assessment (regulatory submissions, database updates)
  • Trains and provides guidance to peers as required
  • Works in a safe manner collaborating as a team member to achieve all outcomes.
  • Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.
  • Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.
  • All other relevant duties as assigned.

Job Requirements

  • Education
    • B.Sc. in chemistry, biology, pharmaceutical, engineering, health sciences or a related field required.
  • Knowledge, Skills and Abilities
    • Must possess strong knowledge of regulatory requirements associated with new drug submissions , and have familiarity with technical/quality / clinical /non clinical aspects associated with these products
    • Excellent communication, presentation and interpersonal skills
    • Excellent conflict management skills
    • Strong organisational skills; ability to work independently and manage priorities
    • Strong Leadership skills
    • Demonstrated knowledge of the new product development process
    • Knowledge of Canadian and US regulatory guidelines a must
    • Knowledge of and experience with the MS-Office suite of products
  • Experience
    • 8+ years progressive experience the pharmaceutical regulatory affairs

At Apotex, we are committed to fostering a welcoming andaccessible work environment, where all everyone feels valued, respected, and supported to succeed.

We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

The hiring range for this position is $ 95,594.40- $ 133,832.16 CAD per year. The final agreed-upon salary may vary based on factors such as job-related knowledge, skills and experience.

We are looking for top talent. If your qualifications differ from those listed above, the scope of work and final agreed-upon salary may be adjusted to reflect your individual qualifications.

The Apotex Total Rewards package goes beyond base salary. Apotex offers bonus programs based on your position in the organization, you can excel based on our pay-for-performance philosophy. With comprehensive benefits, a pension plan to help you save for retirement and learning and development opportunities, we provide a comprehensive package for your personal and professional development.

Apotex will use artificial intelligence to screen, select and/or assess your application for this job.

This job posting is for a role that is currently available and vacant at Apotex.

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