Formulation Development Chemist

Job Summary The Formulation Development Chemist is accountable to and interacts with the Pharmaceutical Development Manager. The formulation development chemist supports all activities required to develop, optimize, scale-up and technology transfer of a stable formulation and its associated manufacturing process, to make it suitable for commercial production as well as subsequent product launch and commercialization activities. The projects include those from internal and external customers. Responsibilities Provides leadership within the pharmaceutical development team, as well as across functional project tactical team.Develops complex new formulations and their corresponding manufacturing processes that is scalable to commercial production setting.Source the excipients used in formulation and the API that meet the regulatory requirement.Conducts experiments with regards to various types of packaging components for product package development.Manufactures pharmaceutical development lab batches which may include:- Weighs, mixes and blends raw materials to produce experimental trials and small-scale batches for solutions and semi-solid formulations.- Records observation on product and process characteristics during experimental trials and propose changes to improve compounding procedure based on observations.- Testing of physical parameters for formulated and Brand Leader product for laboratory, scale-up processes samples and others as required.- Design and conduct accelerated or long-term experiments to establish the physical stability of the formulation so developed. - Set-up and clean all equipment including mixers, homogenisers and tanks.Authors the formulation/processing development protocol and report. Writes-up and signs off various documents such as compounding batch record and demo batch study protocol.Assists in scale-up and technology transfer from pharmaceutical development batch scale to commercial process and trains production operators.Assists with trouble shooting from process development/scale-up to production of stability batches.Develops and writes SOP’s related to formulation work for general lab use.Provides technical support and expert advice to Production during manufacturing of stability batches.Assists in the investigation of process deficiencies of existing formulations to determine the cause and recommends solutions for improvement.Attends external customer project meetings and contributes to the technical discussion.Follows GMP and regulatory requirements and ensures quality standards are met.Follows and supports all safety guidelines and regulations.Demonstrates the Company Mission, Vision and Values Statements, policies, and current standard business practices.Performs other related duties as required. Qualifications EducationB.Sc. Degree in biochemistry, pharmacy, pharmaceutics, chemical engineering, or related area. Masters or Doctorate considered an asset.Experience2 years working experiences in a pharmaceutical formulation laboratory.Experiences in formulation/packaging/process development of liquid and/or semi-solid dosage forms.Proficient understanding of regulatory requirements.Project management experience managing multiple projects simultaneously.Strong communication skills both written and verbal.Ability to work under minimal supervision.Proven analytical and problem-solving skills to resolve routine and non-routine problems.Experience working in a self- directed team environment.Proven time management skills with the ability to balance competing priorities in a deadline driven environment.Starting at approximately [$75,000 CAD]. The final compensation is determined based on qualifications and experience. Total rewards include comprehensive benefits, bonus eligibility, and professional development support.What we offer:Excellent compensation/benefits package.Bonus and reward programsDiscounted gym membershipsPrograms supporting work life balanceEmployee recognition programProfessional and personal development programssocial events and spirit days We are committed to diversity and inclusion, and thank all applicants in advance; however, we will be corresponding only with those selected for an interview.In accordance with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act, we are committed to providing an inclusive and barrier free recruitment and selection process.Recruitment Fraud – please be aware of recruitment fraud. Novocol Pharmaceutical of Canada Inc. will never ask for banking information, moneyor any personal information up front. We will only respond to official applications submitted through our careers site. In addition, we will only use official corporate e-mail addresses (septodont.com or novocolpharma.com) to communicate with applicants. Should you be contacted without submitting an application, please delete the message and advise your e-mail provider.Internal Job Posting Grade 9. The due date for internal applicants to apply for this role is November 18, 2025. Contract type PermanentPosition location