Chemist, R&D

4 weeks ago


Mississauga ON, Canada Candoo Pharmatech Company Inc Full time €47,000

Overview Candoo Pharmatech is seeking a dedicated and detail-oriented Quality Control Chemist to join our dynamic team. In this role, you will provide analytical support for the development of new drug products across various dosage forms. The ideal candidate will perform analytical testing, maintain accurate documentation, ensure compliance with GMP standards, and contribute to the continued success of our R&D and manufacturing operations. Key Responsibilities Perform release, in-process, and stability testing using analytical techniques such as FTIR, KF titration, dissolution, and HPLC assay, in accordance with established methods and SOPs. Conduct purified water monitoring and cleaning validation analyses using a TOC analyzer. Perform daily verification and calibration of laboratory instruments and assist with annual calibrations per SOP requirements. Load and pull stability samples as assigned, following approved procedures. Coordinate with equipment service vendors for preventive maintenance and calibration, maintaining proper documentation for audit purposes. Document all experimental data in compliance with Good Documentation Practices (GDP). Report unexpected or Out of Specification (OOS) results immediately to the Manager, assist in laboratory investigations, and complete CAPA as required. Prepare raw data packages and OpenLab reports for clients as needed. Summarize analytical results and prepare technical reports as assigned. Properly collect and dispose of laboratory waste according to company policy. Maintain a clean, organized, and audit-ready laboratory environment, ensuring compliance with applicable SOPs, regulations, and safety standards. Support internal, client, and regulatory audits. Perform other related duties as assigned. Qualifications Bachelor's degree in Analytical Chemistry, Chemistry, Pharmaceutical Science, or a related discipline. Minimum 1 year of experience in analytical R&D or quality control within the pharmaceutical industry. Hands-on experience with analytical instruments such as HPLC, GC, Dissolution Apparatus, TOC, FTIR, UV, and KF is a strong asset. Solid understanding of cGMP, regulatory compliance, and laboratory safety standards. Self-motivated, detail-oriented, and adaptable to a fast-paced, growth-oriented environment. Strong written and verbal communication skills in English. Excellent organizational and report-writing abilities. About Candoo Pharmatech Candoo Pharmatech Company Inc. is a rapidly growing Contract Development and Manufacturing Organization (CDMO) specializing in advanced drug delivery and formulation development. We focus on high-technical-barrier and difficult-to-formulate solid, semi-solid, and liquid dosage forms. Located in the heart of Mississauga's pharmaceutical business park, our state-of-the-art facility supports our mission to develop high-quality, affordable medicines through innovative technology and strong industry partnerships. At Candoo Pharmatech, we are committed to fostering an inclusive and accessible work environment where all employees feel valued, respected, and supported. Job Types: Full-time, Permanent Pay: From $47,000.00 per year Benefits: Dental care Extended health care On-site parking Paid time off RRSP match Vision care Work Location: In person


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