Chemist I

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials Job Description Work Hours/Shift Information : This role will initially follow normal working hours (8:00 AM - 5:15 PM) for training and may require occasional support for night testing. Once ready, you will transition to a rotating 24x5 shift pattern, and eventually to a 24x7 shift pattern depending on operational needs. Location : 31 Joo Koon Circle, Singapore Position Summary As a Chemist I, you will play a vital role in delivering world-class analytical solutions through outstanding expertise in biologic chemistry. Your work will significantly impact our ambitious projects, ensuring flawless quality control operations that meet regulatory compliance and data integrity principles. You will collaborate closely with other functions, promoting a proactive business partnership to successfully implement method qualifications and validation strategies. Responsibilities Support new equipment qualification, lab computerized systems, and chemistry lab setup. Perform transfer, verification, and validation of laboratory procedures. Prepare technical documentation, including protocols, analytical write-ups, standard operating procedures, specifications, investigations, and reports. Analyze incoming goods, intermediates, and finished products under cGMP conditions for QC release and stability studies. Lead the testing process from sampling to the release of raw materials, drug substances, process aids, and packaging materials. Ensure timely and compliant testing of all chemistry-related analyses, including HPLC, GC, and stability analysis. Manage daily laboratory operations, ensuring compliance with GMP standards. Identify and address compliance gaps with updated pharmacopoeia and regulations. Lead laboratory investigations, deviations, and ensure timely closure in line with quality management systems. Review analytical and laboratory data for accuracy and compliance. Perform maintenance and calibrations on laboratory equipment. Troubleshoot technical issues related to analytical equipment and methods. Manage QC chemical, reference standard, and consumable stock levels. Train fellow chemists, serving as a mentor and expert. Maintain a detailed understanding of international regulatory requirements. Communicate effectively with cross-functional teams and participate in problem-solving activities. Act as a Subject Matter Expert during audits and inspections. Undertake internal audits and support continuous improvement initiatives. Promote a culture of quality and adherence to cGMP, EHS, and 5S standards. Be prepared to support shift work if needed. Minimum Requirements/Qualifications Education : University degree or equivalent experience in chemistry, biochemistry, or life sciences. Experience : At least 2-3 years of proven experience in the pharmaceutical or medical devices industry, with a focus on Quality Control. Knowledge of regulatory expectations including PICS, ICH, Singapore HSA, EMA, and US FDA. Proficiencies : Knowledge and exposure to cGMP environment. Sound technical knowledge of QC chemistry techniques (HPLC, UPLC, CE, etc.). Strong interpersonal and communication skills in English. Ability to work cross-functionally and meet timelines and objectives. Experience with Health Agency/internal audits. 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. #J-18808-Ljbffr