Analytical Chemist

AtomVie Global Radiopharma Inc. is a global leading GMP manufacturer and distributer of clinical and commercial radiopharmaceuticals.

We work with our partners to transform patients' lives by advancing high quality drugs for the treatment and diagnosis of diseases.

We are a community that challenges ourselves professionally, takes pride in what we can accomplish together and values the impact we can make with our partners and patients across the globe.

Start your career with AtomVie today and help us achieve our vision:
to transform lives by revolutionizing healthcare.

About the Role

The
Analytical Chemist is responsible for working in accordance with company policy and within GMPs, while contributing technical expertise to support current products and develop future drugs within the AtomVie portfolio or through support of our CDMO functions.

What You Will Do

• Perform quality control (release & retrospective) testing of incoming materials, drug substances, and finished drug products according to standard testing methods (STMs), including Chemical (e.g. HPLC Assay and Impurities, Radiochemical Puritiy, pH, iTLC, Residual solvents by GC), Biological (e.g. ELISA, IRF, Protein content), and Microbiological (e.g. Bacterial Endotoxin) testing methods. Methods may be compendial (USP, EP) or inhouse methods.
• Coordinate quality control (release &retrospective) testing of drug substances with contract laboratories or contract research organizations according standard testing procedures, USP or EP.
• Conduct analytical method development, transfer, and validation activities: Write routine validation protocols with input from SMEs. Perform routine validation activities independently and more complex validations with guidance, as per approved protocols. Write validation reports according to regulatory guidelines (ICH, USP, etc.) with input from SMEs.
• Conduct all work in accordance with AtomVie Standard Operating Procedures (SOPs) and raise any deviations immediately to the attention of Lab Management and Quality Assurance.
• Conduct peer review of laboratory records; create the release certificate of analysis.
• Write technical documents (e.g. author/create specifications, test reports, data summaries, investigations, CAPAs); prepare CAPA implementation plans and participate in closing laboratory investigations.
• Write (author) new STMs, SOPs controlled forms, data entry templates, etc., provide peer review and provide input for coworkers. Initiate change controls (prepare change control proposal) and revise/improve existing methods.
• Responsible for training other colleagues, colleagues from other departments, and new staff.
• Perform routine quality operations including calibration/maintenance of equipment and inventory/material management of incoming raw materials/container closures and analytical reagents, when required. Troubleshoot systems with guidance from SME.
• Responsible for the housekeeping of the facility including the disposal of hazardous waste (chemical and radioactive) through the appropriate wastestreams. Monitor effectiveness of the housekeeping and waste procedures and propose improvements to management.
• Work as a member of a team to achieve all outcomes; ensure that daily work activities are aligned with a production and stability plan/calendar.
• Responsible for maintenance of documentation to fulfill applicable regulatory requirements relating to nuclear safety (e.g. radioactive material transfer forms).
• Any other duties as assigned.

What You Bring to the Role

• Expertise in working with antibodies, proteins and antibodydrug conjugates, protein characterization, UV/VIS, etc.) and chemical analysis
• Experience in method development and validation, and documentation of such studies, is an asset.
• Experience working with sterile products, working in a BSL2 laboratory, and knowledge of microbiological testing (Bioburden, Sterility, Bacterial Endotoxins) is an asset.
• Knowledge of UV, IR, mass spectrometry, and NMR is an asset.
• Proficiency with spreadsheets (e.g. Excel, Google Sheets); with the ability to rapidly input data and retrieve records, statistics, trends, etc.
• Good writing skills; ability to write technical documents, reports and presentations for customer meetings.
• Excellent communication skills (in English) and ability to work both independently and cooperatively in a team environment

Requirements:

• Degree in Biology, Biological Chemistry, Biotechnology, or a related discipline.
• M.Sc. or Ph.

D is preferred.

• 57 years' handson experience in a pharmaceutical GMP environment,
• Experience in Performing QC testing of materials and products using HPLC, GC, TLC, etc.
• Flexibility in work schedule to support a 7day work week in support of nightshifttype production environment
• Ability to lift 23 kilograms required

AtomVie Offers

• Group Health & Dental Benefits (from day 1)
• RRSP Matching Program
• Perkopolis
• Employee Assistan

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