ZipRecruiter

Log In

1

Pharmaceutical Development Jobs in Ontario (NOW HIRING)

Septodont

Project Manager II

Cambridge, ON

At Septodont, a global leader in dental products and a key player in pharmaceutical development and contract manufacturing (CDMO), we are proud to work every day to improve patients' health and well ...

Bora Pharmaceuticals

Project Manager

Mississauga, ON

CA$81K - CA$101K/yr

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

Bora Pharmaceuticals

Project Coordinator

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 ...

Septodont

Production Operator

Cambridge, ON

At Septodont, a global leader in dental products and a key player in pharmaceutical development and contract manufacturing (CDMO), we are proud to work every day to improve patients' health and well ...

Septodont

Material Handler

Cambridge, ON · On-site

At Septodont, a global leader in dental products and a key player in pharmaceutical development and contract manufacturing (CDMO), we are proud to work every day to improve patients' health and well ...

next page

Showing results 1-20

All JobsPharmaceutical Development JobsPharmaceutical Development Jobs in Ontario

Pharmaceutical Development information

See Ontario salary details

$27.5K

$100.6K

$203.5K

How much do pharmaceutical development jobs pay per year?

As of Aug 25, 2026, the average yearly pay for pharmaceutical development in Ontario is $100,605.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,500.00 and $136,500.00 per year, depending on experience, location, and employer.

What is a pharmaceutical development?

A Pharmaceutical Development job involves researching, formulating, and optimizing new drug products to ensure safety, efficacy, and regulatory compliance. Professionals in this role work on drug formulation, process development, and scale-up for manufacturing. They collaborate with scientists, regulatory teams, and production staff to bring medications from the lab to market. This field requires strong knowledge of chemistry, biology, and regulatory requirements.

What does a pharmaceutical development professional do?

Professionals in Pharmaceutical Development typically oversee the formulation and optimization of new drug products, conduct lab-based experiments, and analyze test data to ensure product efficacy and safety. They frequently collaborate with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing to advance each stage of product development. Regular responsibilities also include drafting technical reports, maintaining detailed laboratory documentation, and supporting regulatory submissions. The role often requires balancing hands-on lab work with strategic planning, ensuring that all processes comply with industry standards and regulations.

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

To thrive in Pharmaceutical Development, you need a strong background in pharmaceutical sciences, chemistry, or related fields, often supported by an advanced degree (MS or PhD) and experience in drug formulation and testing. Proficiency in analytical instrumentation (e.g., HPLC, GC), regulatory compliance systems, and Good Laboratory Practice (GLP) certifications are highly valued. Strong project management, problem-solving abilities, and effective communication skills set top performers apart. These competencies ensure the development of safe, effective pharmaceuticals while navigating complex regulatory requirements and cross-functional team dynamics.

How much do pharmaceutical developers make?

Pharmaceutical developers typically earn a median annual salary of around $80,000 to $120,000, depending on experience, education, and location. Entry-level positions may start lower, while experienced professionals or those with advanced degrees can earn higher salaries, especially in research and development environments.

How to get into pharmaceutical development?

To enter pharmaceutical development, candidates typically need a bachelor's degree in pharmacy, chemistry, biology, or a related field, with advanced roles often requiring a master's or Ph.D. in a relevant discipline. Gaining experience through internships, research projects, or entry-level positions in laboratories is valuable, along with developing skills in laboratory techniques, data analysis, and regulatory compliance. Certifications such as Good Laboratory Practice (GLP) or Good Manufacturing Practice (GMP) can enhance job prospects in this field.

What does a pharmaceutical development do?

A pharmaceutical development professional is responsible for designing, testing, and optimizing processes to create new drugs or improve existing ones. They work in laboratories and manufacturing settings, often using specialized tools and adhering to regulatory standards to ensure product safety and efficacy.

What are popular job titles related to Pharmaceutical Development jobs in Ontario?

For Pharmaceutical Development jobs in Ontario, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Development jobs in Ontario look for?

The top searched job categories for Pharmaceutical Development jobs in Ontario are:

Pharmaceutical Development jobs near you
Infographic showing various Pharmaceutical Development job openings in Ontario as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 21% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $100,605 per year, or $48.4 per hour.

Scientist, Product Development

Apotex

Richmond Hill, ON • On-site

Full-time

Retirement

Re-posted 7 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.

Apply