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Pharmaceutical Formulation Development Jobs in Ontario

Mechanic - Pilot Plant

Mississauga, ON · On-site

CA$68K - CA$85K/yr

About Bora Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing ...

Project Coordinator

Mississauga, ON · Hybrid

CA$68K - CA$85K/yr

About Bora Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing ...

... phase formulation development to clinical trial material to commercial supply -- within the same ... or pharmaceutical industries. 1 - 3 years millwright experience, preferred Experience reading ...

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Pharmaceutical Formulation Development information

See Ontario salary details

$13

$37

$61

How much do pharmaceutical formulation development jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for pharmaceutical formulation development in Ontario is $37.44, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $43.03 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in pharmaceutical formulation development?

To thrive in Pharmaceutical Formulation Development, you generally need a strong background in pharmaceutical sciences, chemistry, or related fields, and experience with drug formulation principles and analytical techniques. Familiarity with laboratory instrumentation (such as HPLC, dissolution testers), regulatory documentation systems, and GMP/GLP compliance is essential. Excellent problem-solving abilities, attention to detail, and cross-functional communication skills help you excel in a team-oriented environment. These competencies ensure the creation of safe, effective, and commercially viable pharmaceutical products that meet regulatory standards.

What are the main responsibilities of someone working in pharmaceutical formulation development?

Professionals in Pharmaceutical Formulation Development are typically responsible for designing and optimizing drug formulations, conducting laboratory experiments, and ensuring products meet safety, efficacy, and stability standards. Their work often involves collaborating closely with analytical, manufacturing, and regulatory teams to advance products from early development to commercial scale-up. They may also troubleshoot formulation issues, document experimental results, and contribute to regulatory submissions. The role requires careful attention to detail, a strong scientific foundation, and the ability to work both independently and as part of a multidisciplinary team.

What is pharmaceutical formulation development?

A Pharmaceutical Formulation Development job involves designing and optimizing drug formulations to ensure safety, efficacy, and stability. Professionals in this role work on selecting appropriate excipients, determining dosage forms, and improving drug delivery methods. They collaborate with regulatory teams to meet compliance standards and conduct tests to assess product performance. This role is essential for bringing new medications from the research phase to commercial production.

What are popular job titles related to Pharmaceutical Formulation Development jobs in Ontario? For Pharmaceutical Formulation Development jobs in Ontario, the most frequently searched job titles are:
What job categories do people searching Pharmaceutical Formulation Development jobs in Ontario look for? The top searched job categories for Pharmaceutical Formulation Development jobs in Ontario are:
Infographic showing various Pharmaceutical Formulation Development job openings in Ontario as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $77,879 per year, or $37.4 per hour.

Scientist, Product Development

Apotex

Richmond Hill, ON

Other

Retirement

Posted 24 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.