Analytical Development Chemist II

2 weeks ago


Cambridge, Canada Novocol Pharma, a Septodont company Full time

Analytical Development Chemist II – Novocol Pharma, a Septodont company Novocol Pharma is a growing contract development and manufacturing organization (CDMO) specialized in sterile injectable cartridges and combination product manufacturing. With over 40 years in operation and a team of 600 employees, the Cambridge, Ontario facility delivers customer‑centric value across global pharmaceutical projects. Job Summary The Analytical Development Chemist II is accountable to the Pharmaceutical Development Manager and focuses on analytical development, validation, and support for Novocol Pharma CDMO projects and Septodont dental projects. The role involves training, problem‑solving, and documenting analytical methods. Responsibilities Develop, validate, transfer, and verify analytical methods for testing raw materials, bulk, and finished products using equipment such as UV, GC, HPLC, UPLC, LC/HRMS, LC/MS, etc. Support the generation of method development, validation, verification, and transfer protocols and reports. Develop specifications for release and stability testing of raw materials, packaged components, bulk, and finished products. Perform analytical testing and evaluation of raw materials, finished products, and stability samples of development batches, including R&D experimental formulation samples. Record and report all lab data per approved procedures and regulatory requirements. Ensure all work is performed and documented in accordance with company policies, procedures, cGMP, and health & safety requirements. Maintain a clean and safe laboratory environment. Serve as SME for selected equipment in the Pharmaceutical Development laboratory. Observe and support all safety guidelines and regulations. Demonstrate company Mission, Vision, and Values Statements, policies, and current standard business practices. Perform other related tasks/duties as required. Qualifications Education B.Sc., MSc, or PhD in analytical chemistry, biochemistry, or a related field. Experience Minimum 3 years developing GC and HPLC/UPLC analytical methods. Preferred experience testing biological products such as peptides, proteins, and vaccines. Good working knowledge of LC/MS with at least 1 year of experience in LC/MS method development or use. Proven analytical and problem‑solving skills for routine and non‑routine challenges. Proficient understanding of regulatory requirements. Laboratory data recording skills. Strong organizational, interpersonal, and communication skills, both written and verbal. Benefits Excellent compensation and benefits package. Bonus and reward programs. Discounted gym memberships. Work‑life balance programs. Employee recognition program. Professional and personal development programs. Social events and spirit days. Contract Type Permanent Seniority level Mid‑Senior level Employment type Full‑time Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Other Information We are committed to diversity and inclusion. In compliance with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act, we provide an inclusive, barrier‑free recruitment and selection process. Recruitment Fraud – do not share banking info, money, or personal data. Official applications must be submitted through our careers site and communications will come from official corporate email addresses. Internal Job Posting Grade 8. The due date for internal applicants to apply for this role is November 18, 2025. #J-18808-Ljbffr



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