Technologist, Quality Control

Applied Pharmaceutical Innovation (API) brings life-saving research to the real world by helping life science innovators bridge the gap between academic research and commercial product development. We are driven, compassionate, and laser focused on making a dramatic positive impact with everything we undertake.

When you join API, you are part of a rapidly growing team that is creating collaborative opportunities to commercialize Canadian life sciences discoveries, increasing the amount of commercial research and development in the country, and supporting Alberta as a key pillar in Canada’s life sciences sector.

The Technologist, Quality Control plays a critical role in ensuring product quality and regulatory compliance by performing a range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products, particularly drug substances and drug products utilizing techniques such as HPLC, GC, UV-Vis, FTIR, and others. The Technologist, Quality Control ensures accurate, GMP-compliant testing and documentation. The role supports equipment qualification, method transfer, data integrity through LIMS, development of Quality Control documentation, and continuous improvement initiatives.

Please note this position requires full-time on-site presence.

Key Responsibilities:

Testing & Analysis:

• Perform laboratory tests on raw materials, in-process materials, packaging materials, and finished products, particularly APIs and finished dosage forms, following established SOPs.
• Utilize analytical techniques such as HPLC, UHPLC, GC, UV-Vis, FTIR, viscosity, osmolality, and titration to assess product quality.
• Ensure sample and data traceability throughout testing.
• Accurately calculate and analyze data to reflect raw data, ensuring test controls and monitors are properly recorded.
• Maintain accuracy and efficiency in testing, documenting results in compliance with GMP and GLP standards.
• Assist QC Manager to perform OQ, and PQ of laboratory equipment in collaboration with suppliers.
• Assist in developing and validating analytical methods for new products or processes.
• Continuously suggest optimizing instrument results by refining parameters or adjusting setups.

Documentation & Compliance:

• Maintain accurate records of testing data, observations, and calculations in compliance with regulatory requirements and GMP standards.
• Review and evaluate test results to ensure they meet specifications.
• Prepare and review Certificates of Analysis (COA) for raw materials, intermediates, and finished products.
• Assist the QC Manager in implementing quality-related software systems, particularly LIMS and LabX.
• Manage laboratory workflows and data through LIMS to ensure seamless operations and data retrieval.
• Document QC equipment qualifications, calibration, and maintenance.

Quality Control Procedures:

• Develop and compile SOPs for new instruments and procedures, including OOS, analytical validation, verification, technical transfers, and stability testing.
• Conduct investigations and root cause analyses for deviations, out-of-spec results, or complaints.
• Support the QC Manager in OOS investigations, non-conformance (NC) reports, CAPAs, and product complaints.
• Initiate QC-related change controls and prepare written procedures, including SOPs and other protocols for analysis.
• Assist in performing OQ and PQ of laboratory equipment in collaboration with suppliers.
• Support the development and validation of analytical methods for new products or processes.
• Contribute to the implementation and continuous improvement of QC processes and quality systems.

Team Collaboration & Communication:

• Collaborate with Production, Quality Assurance, R&D, and Regulatory Affairs teams to ensure alignment on quality objectives and timely product release.
• Support internal quality audits and external inspections, ensuring compliance with regulatory standards and inspection readiness.
• Provide technical support to cross-functional teams as needed.
• Review peer's work to ensure compliance and quality.

Training & Development:

• Stay updated on industry trends, regulatory changes, and new technologies in the pharmaceutical field.
• Participate in training sessions and continue to develop materials for training new QC staff.

Occupational Health and Safety:

• Comply with workplace policies and procedures pertaining to environmental health and safety (EHS).
• Adhere to company policies, procedures, and regulations for maintaining a clean and safe work environment, including work areas, instrumentation, and testing materials.

Qualifications:

Education:

• M.S., B.S., or Technological degree, or a degree in Chemistry, Biochemistry, Pharmacy, or a related scientific field.

Experience:

• Strong knowledge of analytical testing in GMP environment.
• Hands-on experience with analytical instruments such as HPLC, GC, IR, UV-Vis spectrophotometry, and other laboratory equipment.
• Strong understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other regulatory requirements (FDA, EMA, ICH).
• 3-5 years of experience in GMP QC laboratory or similar pharmaceutical production settings is preferred.
• Experience with LIMS for managing laboratory data, sample tracking, and documentation processes is preferred.
• Experience working in ISO-17025 environment is an asset.

Personal Competencies:

• Strong oral and written communication skills, with the ability to handle confidential information and frequent internal and external interactions.
• Excellent attention to detail and critical thinking.
• Ability to manage time effectively and prioritize tasks in a fast-paced environment.
• Occasional moderate physical activity, including standing, walking, lifting, and keyboarding.
• Ability to meet deadlines and troubleshoot problems efficiently.
• Ability to work independently and as part of a team to achieve organizational objectives.
• Technically adaptable, flexible, and forward-thinking.
• Committed to continuous learning, reviewing scientific literature, and staying current with new technical and scientific information.
• Proficiency in Microsoft Office applications (Word, Excel, Outlook) and business-related software, such as Open Lab, Empower, or similar applications, with the ability to learn company-specific software.

Working Conditions:

• This position requires on-site presence.
• Exposure to production environment.
• Work in production and office settings.

Additional Required Documents to Support Application:

• Applications submitted without a resume AND cover letter will not be reviewed.

Perks and Benefits at API:

• Comprehensive Health Coverage: At API, we prioritize the well-being of our employees. We offer a comprehensive health coverage plan. Our premiums are 100% covered, ensuring that you and your dependents receive the necessary healthcare support.
• Payment in Lieu of Pension: API provides an additional 15% of your annual base salary, as an alternative to traditional pension benefits.
• Professional Development Opportunities: We foster a culture of continuous learning and growth. API provides access to various professional development opportunities, including training programs, workshops, conferences, and certifications.
• Collaborative and Inclusive Environment: At API, we believe in the power of collaboration and diversity. We foster an inclusive work environment that values and respects individuals from all backgrounds.
• Generous Paid Time Off: We understand the importance of taking time off to recharge and maintain a healthy work-life balance. API offers a generous paid time off (PTO) policy that includes vacation days, medical/personal days, and holidays.
• Green Transit Allowance: Employees based out of an office are eligible to enroll in our green transit program, which promotes the use of environmentally friendly modes of transportation.
• Work From Home: Eligible employees are entitled to 10 Work from Home days, this is subject to job function, company needs, and manager approval.

How to Apply:

Interested applicants must submit a resume and cover letter expressing their interest in the position and why they believe they are a strong candidate.

We appreciate all applicants' interest and will only contact those selected for interviews.

If you have any questions about the application process or require accommodations during the hiring process, please contact careers@appliedpharma.ca.

Our team, clients, and stakeholders come from a variety of backgrounds. In recruiting for our team, we welcome the unique contributions that all people bring to the workplace in terms of varied lived experiences, education, culture, gender, race, sexual orientation, religious or ethnic background, neurodiversity, and cognitive and physical ability.

Before employment, successful candidates will be required to meet the requirements of a pre-employment screening, which includes background reference checks, educational credential verification, and criminal reference checks.

Application Deadline: May 6, 2025