Quality Control Technician

The Opportunity: Responsible for completing product quality checks, conducting routine testing and analysis of production output, reviewing quality checks for accuracy, and documenting quality control issues as needed. Communicates with quality control, quality assurance and production teams to provide or obtain information requiring some explanation. Carries out day-to-day objectives following defined procedures, addressing recurring problems with known solutions and resolving more complex issues using experience and available support. Key Responsibilities Conduct inspection and testing of raw materials and finished goods to ensure compliance with quality standards. Develop, implement, and enforce quality control procedures and standards. Document inspection results, test data, and quality reports accurately and promptly. Identify quality issues with escalation to direct reporting Maintain laboratory inventory using KANBAN systems for chemicals and consumables. Perform routine and non-routine chemical testing on raw materials and finished products. Operate laboratory instruments (e.g., pH meter, conductivity meter, UV spectrophotometer, Karl Fischer titrator, FTIR, titration apparatus) in accordance with SOPs. Follow established test methods and compendial standards (USP, EP, BP, JP, ACS) and EXCIPACT guidelines. Analyze test results, calculate data, and prepare reports to verify compliance with specifications. Review laboratory data forms, including water testing and direct measurement analyses. Arrange Calibrate, maintain, and troubleshoot laboratory equipment to ensure optimal performance. Record final results and raw data in the SAP system. Support investigations, customer complaints, and troubleshooting activities through detailed analytical review. Apply appropriate disposition labels to materials (e.g., accepted, rejected, quarantined). Handle hazardous materials in compliance with safety protocols and using appropriate PPE. QUALIFICATIONS (Education/Training, Experience and Certifications) Diploma in Chemistry, Microbiology, Biotechnology, or a related scientific discipline_ /or ITE Certificate or Higher Nitec in Chemical Process Technology, Biotechnology, Environmental Science, or a related discipline. Formal training in laboratory practices, analytical techniques, and GMP/GLP standards is preferred. Experience Minimum 2–3 years of hands-on experience in a Quality Control laboratory within the pharmaceutical, chemical, or life sciences industry. Experience with compendial testing (USP, EP, BP, JP) and working in cleanroom environments is an advantage. Familiarity with SAP and equipment calibration is desirable. Certifications Certification in Good Laboratory Practices (GLP), ISO standards (e.g., ISO 9001, ISO 17025), or EXCiPACT is a plus. Safety training for handling hazardous materials and PPE usage is required. KNOWLEDGE SKILLS AND ABILITIES (Those necessary to perform the job competently) Applied working knowledge of various laboratory instrumentation Ability to work collaboratively in a diverse team environment with people at all levels in the organization Proficiency in Microsoft Word, Power Point, Excel and Access Strong problem solving and analytical skills ENVIRONMENTAL WORKING CONDITIONS & PHYSICAL EFFORT (Under Typical Positions) Typically works in an office environment with adequate lighting and ventilation and a normal range of temperature and noise level. At times, may be exposed to a variety of different chemicals including flammables, corrosives, oxidizers, and others. Work assignments are diversified. Examples of past precedent are used to resolve work problems. New alternatives may be developed to resolve problems. A frequent volume of work and deadlines impose strain on routine basis. Minimal physical effort is required. Work is mostly sedentary but does require walking, standing, bending, reaching, lifting, or carrying objects that typically weigh less than 10 lbs. May be required to work on a shift schedule (e.g., 3:00 PM to 12:00 AM) or over time to support ad hoc business demands. Ability to communicate effectively, both verbally and in writing Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement: We are an Equal Employmen