Project Manager, New Product Development (Regulatory Affairs)

APOTEX; Toronto; On-site; CAD 96,000 - 134,000; Full time

Benefits offered by this job

Bonus program

Pension plan

Learning and development

Job summary

Apotex in Toronto seeks a Project Manager for New Product Development in Regulatory Affairs to lead submissions and due diligence for opportunities in the NPD portfolio. You will collaborate with internal teams and external partners to develop regulatory strategies, manage risks, and guide deficiency responses to support timely product launches across global markets.

This role emphasizes strong coordination, leadership, and adherence to ethics, quality and safety policies within a dynamic

Qualifications

• B.Sc. in chemistry, biology, pharmaceutical, engineering, health sciences or a related field required.
• Strong knowledge of regulatory requirements for new drug submissions.
• Canadian and US regulatory guidelines knowledge is a must.
• Excellent communication and leadership skills.
• Experience in pharmaceutical regulatory affairs is required.

Responsibilities

• Develops regulatory project strategy with appropriate risk mitigation.
• Ability to recover projects that are at risk.
• Prepares/leads regulatory submissions according to current requirements.
• Assesses potential deficiencies and works to address prior to submission.
• Leads development of deficiency response strategies with stakeholders and finalizes responses by target dates.
• Conducts thorough due diligence of opportunities with the Business Development team.
• Supports seamless product launches through timely review of changes and documentation.
• Executes change control assessments and related regulatory activities.
• Trains and provides guidance to peers as required.
• Works safely and collaboratively to achieve outcomes.
• Demonstrates behaviours aligned with Collaboration, Courage, Perseverance, and Passion.

Skills

Regulatory knowledge

Submissions

Leadership

Communication

Project management

Education

B.Sc. in science/engineering

Tools

MS Office

Job description

Project Manager, New Product Development (Regulatory Affairs)

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.

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.