Job Title

**Work Schedule** Second Shift (Afternoons) **Environmental Conditions** Office **Job Description** **Summary** Responsible for independently reviewing pharmaceutical laboratory documentation, raw data, and analytical reports generated in Lab Operations. The candidate must be familiar with pharmaceutical laboratory analysis and GMP requirements. **This is a 12 month fixed contract position. The working hours are M-F 1:00pm-9:30pm. **Essential Functions** Review, with minimal supervision, routine pharmaceutical laboratory technical documents (e.g., batch testing, stability testing, and method validation) and associated raw data generated in Pharmaceutical Laboratories, ensuring high quality and delivery within agreed timelines. Ensure lab test methods, protocols, and Standard Operating Procedures (SOPs) are properly followed by laboratory chemists. Demonstrate familiarity with pharmaceutical laboratory analytical systems and equipment such as Empower software, LIMS, HPLC, UV, pH meters, etc. Verify the integrity, accuracy, and traceability of all data generated and reported by laboratory chemists. Follow up with laboratory chemists to ensure all required corrections are addressed in compliance with Good Manufacturing Practice (GMP) standards. Notify the department supervisor of omissions, incomplete testing results, or other irregularities. Maintain a safe working environment and report potential hazards. Perform afternoon shift work, as required by business needs Travel to different sites as required by business needs. **Required Qualifications** **Education:** Bachelor of Science in Chemistry or a related scientific discipline. **Experience:** 1u20133 years of pharmaceutical analytical laboratory experience. **Equivalency:** Equivalent combinations of education, training, and relevant work experience may be considered. **Knowledge, Skills, and Abilities** Familiarity with laboratory analytical technologies, including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet (UV) spectroscopy, titration, and raw material testing. GMP chromatography experience, specifically with Empower software. Direct pharmaceutical laboratory experience in a GMP-regulated environment. Understanding of Good Manufacturing Practices (GMP), International Council for Harmonization (ICH) guidelines, and U.S. Food and Drug Administration (FDA) requirements. Strong organizational skills and attention to detail. Ability to prioritize tasks and meet deadlines. Strong written and verbal communication skills. Demonstrated proficiency in Microsoft Office applications. Proficiency in English. **Standards and Expectations** Follow all Environmental Health & Safety policies and procedures. Work collaboratively with team members, modeling positive team behaviors and partnering to meet project and departmental objectives. Perform all duties in strict compliance with Thermofisher quality systems SOPs and GMP requirements. Maintain a clean and orderly workspace. Actively engage in departmental systems to support efficient workflow (e.g., visual management, scheduling systems, Smartsheet system). Maintain a strong client and patient focus at all times. Understand Key Performance Indicators (KPIs) and contribute to team performance improvement by identifying system enhancement opportunities and participating in problem-solving initiatives. Demonstrate adaptability and openness to change, supporting shifts in priorities and new ways of working. Proactively identify opportunities to improve procedural execution. Communicate risks to timelines proactively. Continuously develop skills and knowledge within the field. **Physical Requirements** Position requires standard ambulatory skills and physical coordination to move within laboratory and office environments. Ability to: Stand, walk, stoop, kneel, and crouch for extended periods. Lift, carry, and move light to medium weights (10u pounds). Use arm, hand, and finger dexterity for grasping and typing for extended periods. Maintain visual acuity to operate equipment, use a computer, and read materials for extended periods. Sit, reach, talk, and hear for prolonged periods. Use of Personal Protective Equipment (PPE) may be required, including safety glasses, safety shoes, lab coat, gloves, safety apron, and occasionally an organic respirator. **Disclaimer** This job description outlines the general nature and level of work performed in this role. It is not intended to be a comprehensive list of all responsibilities, duties, or qualifications. Managers and supervisors may assign additional duties as needed. Nothing contained herein shall be construed to create an employment contract. Requirements may be expressed in brief terms. All language is intended to comply with applicable legislation in each country of operation, including alignment with the EU Equality Directive regarding recruitment and employment practices. **Compensation** The salary range estimated for this position based in Ontario is $41,900.00u2013$62,900.00. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.