Pharmaceutical Formulation Chemist - Strathroy, ON, Canada - Catalent

Description

Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide.

Your talents, ideas, and passion are essential to our mission:
to help people live better, healthier lives.

Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.

the Formulation Scientist will execute on assigned aspects of pre-formulation studies, formulation development and optimization studies, and informal and formal stability studies as directed with quality, speed and efficiency supporting multiple projects in the portfolio.

The Scientist will have familiarity with various aspects of the drug development process in a regulated environment, including topics such as Quality by Design (QbD), Design of Experiment (DOE), and compliance with all regulatory guidelines, all while maintaining patient first culture.

The Scientist will be able to work independently with direction from senior members within the group.

This position is located in Strathroy, Ontario, one of two sites located in Canada offering softgel development and manufacturing capabilities for the Pharmaceutical and Consumer Health industries.

We have a broad range of integrated formulation, manufacturing, analytical and packaging services to offer full-service turnkey solutions.
Execute against assigned formulation lab activities with quality, speed, and efficiency to ensure on-time delivery.
Working knowledge and consistent execution of formulation development, excipient compatibility assessment, data analysis and good documentation practices
Independently execute technical aspects associated with formulation development.

Participate in the development and troubleshooting of formulations and assessment techniques in a timely manner to support internal and customer needs, complaints, and investigations.

Understanding and communication of risks, mitigation, and contingency planning
Presentation of project information at local reviews and with customers as appropriate
Maintain compliance with training, best practices, safety, and cleaning requirements and operate under and maintain GMP/GLP conditions.

Must be able to work extended hours, weekends as needed, especially when problems occur or when deadlines must be met and perform other duties as required.

Bachelor's degree in science or related field is required. (MSc Degree is an asset.
Minimum 1+ years of experience in a formulation's role in a lab setting is preferred.
Experience working in a manufacturing, pharmaceutical and/or GMP facility is asset.
Skilled in the use of Microsoft Office.
There is also the potential exposure to chemicals.
Comprehensive Benefit Package (Health, Dental, Vision, & Life Insurance)
Group Retirement Savings -Registered Pension Plan (RPP) with employer contributions.

Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.

Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to .

This option is reserved for individuals who require accommodation due to a disability.

Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.