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Associate Scientist Product Development Jobs in Ontario

Job Summary Formulation Development - New Products supports all activities required to develop, optimise a stable liquid dose formulation to make it suitable for commercial production. The Scientist ...

... new products, and key performance indicators/lean lab metrics Author, revise, and/or review ... the development of associated training content Communicate technical issues and activity status ...

We'relooking for an experiencedmedical device product development engineerwith exceptionalproject ... You'llthrive in a collaborative environment where complexmedical, life science, and diagnostic ...

You'll thrive in a collaborative environment where complex medical, life science, and diagnostic ... Role Responsibilities As a Product Development Team Lead reporting to the VP Product Development ...

Lead Engineer, Product Development

Mississauga, ON · On-site

CA$94K - CA$132K/yr

  • Medical

  • Retirement

We are pioneers in foam technology science and provide our products to customers in multiple ... Role Purpose: Lead product development activities and projects that translate market needs ...

Product Manager

Mississauga, ON · On-site

CA$100K - CA$130K/yr

Contribute to the development and execution of product strategy and roadmap initiatives * Identify ... Partner with engineering, UX, data science, revenue, and customer success teams * Support go-to ...

The purpose of this role is to conduct scientific research and develop process control for plastic ... It will also involve the development of a product strategy roadmap and product vision for emerging ...

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Associate Scientist Product Development information

What are some common challenges faced by an associate scientist in product development, and how can they be addressed?

Associate Scientists in Product Development often encounter challenges such as balancing tight project timelines with the need for thorough experimental design and data analysis. They may also need to quickly adapt to changing project priorities or troubleshoot unexpected results in the lab. Collaborating effectively with cross-functional teams, such as quality assurance, manufacturing, and regulatory affairs, is essential to overcome these hurdles. Proactively communicating progress, seeking feedback, and staying organized can help Associate Scientists navigate these challenges and contribute successfully to product advancement.

What does an associate scientist in product development do?

An Associate Scientist in Product Development plays a crucial role in researching, designing, and testing new products or formulations in industries like pharmaceuticals, biotechnology, or consumer goods. They conduct laboratory experiments, analyze data, and collaborate with cross-functional teams to improve product performance and ensure regulatory compliance. Their work helps bring innovative and safe products to market efficiently.

What is the difference between Associate Scientist Product Development vs Associate Scientist Quality Control?

AspectAssociate Scientist Product DevelopmentAssociate Scientist Quality Control
CredentialsBachelor's or Master's in Life Sciences, Chemistry, or related fieldBachelor's or Master's in Life Sciences, Chemistry, or related field
Work EnvironmentResearch labs focused on product formulation and innovationLaboratories conducting testing and quality assurance of products
Industry UsageUsed in pharmaceutical, biotech, and consumer goods companiesCommon in manufacturing and quality assurance departments
Search IntentComparing roles in product development and formulationLooking into quality testing and compliance roles

Associate Scientist Product Development and Associate Scientist Quality Control are both entry-level roles in the life sciences industry. While they share similar educational backgrounds, the former focuses on creating and improving products, whereas the latter emphasizes testing and ensuring product quality. Both roles are essential in bringing safe, effective products to market, but they differ in daily tasks and objectives.

What are the key skills and qualifications needed to thrive as an associate scientist in product development?

To thrive as an Associate Scientist in Product Development, you typically need a degree in chemistry, biology, or a related field along with strong laboratory and analytical skills. Familiarity with laboratory information management systems (LIMS), analytical instrumentation (such as HPLC or GC), and relevant regulatory guidelines is often required. Attention to detail, teamwork, and effective problem-solving are vital soft skills for success in collaborative and fast-paced environments. These abilities ensure the accurate development, testing, and optimization of products while maintaining compliance and fostering innovation.

What are popular job titles related to Associate Scientist Product Development jobs in Ontario?

For Associate Scientist Product Development jobs in Ontario, the most frequently searched job titles are:

What job categories do people searching Associate Scientist Product Development jobs in Ontario look for?

The top searched job categories for Associate Scientist Product Development jobs in Ontario are:

What cities in Ontario are hiring for Associate Scientist Product Development jobs?

Cities in Ontario with the most Associate Scientist Product Development job openings:

Infographic showing various Associate Scientist Product Development job openings in Ontario as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 22% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution.

Scientist, Product Development

Apotex

Richmond Hill, ON

Full-time

Retirement

Posted 26 days ago


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

Formulation Development - New Products supports all activities required to develop, optimise a stable liquid dose formulation to make it suitable for commercial production. The Scientist, Formulations Development works under the direction of Senior members of the Formulations Development team to support the development and enhancement of pharmaceutical formulations, manufacturing processes and selection of packaging components. This role includes development of liquids dosage forms for ANDA, ANDS and 505b2 submissions. The dosage forms include both sterile and non-sterile liquid products, not limited to oral, Nasal, ophthalmic, and injectable dosage forms etc.

Job Responsibilities
  1. Perform literature search, collect relevant scientific information and materials, and prepare comprehensive pre-development summaries.
  2. Design, execute, and monitor formulation development experiments using Quality by Design (QbD) principles to develop robust and scalable product compositions.
  3. Collaborate with Formulation Development (FD) and Analytical Development (AD) teams to:
    • Prepare Reference Listed Drug (RLD) characterization reports
    • Define Quality Target Product Profiles (QTPP)
    • Identify Critical Quality Attributes (CQAs)
  4. Conduct risk assessments as per QbD guidelines and develop Design of Experiments (DoE) for:
    • Composition optimization
    • Identification of Critical Material Attributes (CMAs)
    • Evaluation of Critical Process Parameters (CPPs)
  5. Lead the design, development, and optimization of complex sterile and injectable dosage forms, ensuring alignment with regulatory expectations (e.g., FDA, ICH guidelines).
  6. Compile, analyze, and interpret stability data, collaborate with Analytical Development to identify trends, and optimize formulations as required.
  7. Apply strong scientific fundamentals and innovative problem-solving approaches to investigate and resolve complex formulation challenges, including implementation of unconventional techniques when needed.
  8. Develop and implement robust formulation strategies based on QbD and regulatory requirements.
  9. Conduct statistically designed experiments (e.g., factorial design) to meet development objectives and ensure process understanding.
  10. Author, review, and manage technical and regulatory documentation, including:
  • Drug product development sections of dossiers (IND/NDA/ANDA)
  • CMC sections
  • Technical reports, protocols, and summaries
  1. Collaborate cross-functionally with Technical Services, Operations, Regulatory Affairs, and other stakeholders to ensure successful product development and lifecycle management.
  2. Support technology transfer, scale-up activities, and regulatory submissions, including responses to regulatory queries.
  3. Perform additional scientific, technical, or project-related duties as required.
Job Requirements
  • Education & Experience
  • Bachelor's degree (Minimum 5 - 8 years of experience, preferably in a pharmaceutical development environment). Master's degree or PhD in Pharmacy, Pharmaceutical Technology, science or engineering is preferred.
  • Knowledge, Skills and Abilities
    • Excellent working and theoretical knowledge of liquid dosage formulations, sterile and non-sterile manufacturing, combination product requirements.
    • 5+ years of hands-on experience in respiratory and/or nasal drug delivery. 3+ years of hands-on experience in sterile/Injectable pharmaceutical formulation development
    • Proven track record of successful formulation development and commercialization.
    • Experience with statistical design of experiments (DOE) and data analysis.
    • Excellent organization and report writing skills. Advance level of computer skills in Microsoft Office (Word, Excel, PowerPoint and Outlook).
    • Good knowledge of cGMP and regulatory requirements.

At Apotex, we are committed to fostering a welcoming and accessible 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 $ 77,284.85 - $ 101,198.79CAD 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.