Chemist 1- SAS

Chemist 1- SAS Novocol Pharma, a Septodont company is hiring a Chemist I for an 18‑month contract in our Stability and Analytical Services department. Company Details Novocol Pharma is a growing contract development and manufacturing organization (CDMO), specialized in sterile injectable cartridges and combination product manufacturing. We strive for excellence and customer‑centricity to deliver value to global pharmaceutical clients through contract services for drug development and commercial manufacturing. With over 40 years in operation, our team of 600 employees and modern facilities, located in Cambridge, Ontario provide a personalized and responsive experience for our customers. We are focused on serving our strategic partners and patients with quality, integrity, and value. Our employees are our number one asset We offer developmental opportunities, excellent compensation and benefit programs, discounted gym memberships, work/life balance programs, employee recognition, social events and spirit days. We are a proud member of the Septodont group of companies. Septodont is a pharmaceutical and medical device company with a global leadership position in dental pain management. The group counts over 2000+ employees worldwide and has remained a 100% family owned company for over 90 years. Our Cambridge facility serves as a significant manufacturing site within the Septodont group with high volume dental anesthetic production for a global customer base. Job Summary The Chemist I is an entry‑level position accountable to the Department Supervisor. This position is responsible for performing various analytical activities associated with incoming materials, bulk, finished products, stability and complaints. Responsibilities Completes testing in accordance with internal policies, procedures and specifications. Reviews testing performed by other analysts as needed. Maintains and calibrates laboratory equipment. Provides support during internal and external audits as required. Follows GMP and regulatory requirements, and ensures quality standards are met. Notifies management of deviations, out of trend, suspect or out of specification results in a manner and participates in investigations as necessary. Observes 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 assigned. Focus Areas Stability and Analytical Services – Performs testing of stability samples using HPLC, UPLC, ICP‑OES, GC, ion chromatograph, optical comparator and other wet chemistry techniques. Raw materials – Performs chemical testing of commercial raw materials, including excipients and APIs as well as some operating supplies. Bulk/Finished Product/Complaints – Performs chemical and functionality testing for commercial drug product samples, including bulk, in‑process, finished product and complaints. Components/Operating Supplies/Imported Finished Products – Tests incoming materials used by production for commercial products (e.g., primary components, printed materials, operating supplies, secondary components, devices). Technology transfer – Performs transfer of analytical methods from CDMO and R&D labs to the Stability and Analytical Services department. Qualifications Education Degree or diploma in Chemistry or related discipline. Experience One to two years of experience in the pharmaceutical or related industry is an asset. Strong attention to detail. Proven analytical skills with the ability to solve problems. Proficient time‑management skills with the ability to manage multiple priorities. Ability to work in a self‑directed team environment. Proficiency with Microsoft Office applications, especially Excel. Experience with Empower and LIMS is an asset. What we offer Excellent compensation/benefits package. Discounted gym memberships. Programs supporting work‑life balance (EAP). Corporate discounts and perks. Employee recognition program. Social 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. Internal Job Posting Grade 7. The due date for internal applicants to apply for this role is November 18, 2025. Contract type: Contract Seniority level Entry level Employment type Contract Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Novocol Pharma, a Septodont company by 2x. #J-18808-Ljbffr