At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Quality**Job Sub Function:** Quality Control**Job Category:** Professional**All Job Posting Locations:** Huejotzingo, Puebla, Mexico**Job Description:** **Main Duties and Responsibilities:** * Performs test reporting according to data integrity and GMP requirements. * Initiates identified Quality Issues according to applicable procedures, participates in investigations, performs investigation analysis, and provides necessary information to enable CAPA implementation. * Ensures trainings are completed on time in ComplianceWire (Learning Management System) and that all tasks are performed only after completing training on current effective procedures. * Works as authorized personnel for handling controlled substances according to laboratory procedures when applicable; as well as handling the controlled substances module in eLIMS, when applicable. * Performs method transfers and validates R&D or customer testing methods according to required procedures. * Performs cleaning tasks to maintain a clean and organized work environment. * Ensures proper use of assigned resources for carrying out activities, including correct handling of equipment, PPE, reagents, glassware, consumables, and facilities. Reports any violations or deviations in their handling. * Prepares protocols, executes protocols, and generates reports related to Analytical Method Validation and Transfer. * Performs other job-related duties assigned by the supervisor. **Minimum Qualifications:** * QFB, IQ or related field * 2 years of experience in the pharmaceutical or related industry. * Basic to intermediate English. **Other Requirements:** * Compliance with GMP, EHS, WWRIM, AE/PQC, IAPP, and other legal or local regulatory requirements. * Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in analytical or biological testing procedures. * Proficient in using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint). * Ability to lift up to 20 pounds. * Ability to efficiently cooperate with different colleagues. * Project management knowledge desirable. * HPLC operation skills. * Knowledge of pharmacopoeias. * undefined *Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation,**external applicants please contact us via* *https://www.jnj.com/contact-us/careers* *. internal employees contact AskGS to be directed to your accommodation resource.* **Required Skills:** **Preferred Skills:** Analytical Reasoning, Business Behavior, Compliance Management, Continuous Improvement, Controls Compliance, Data Analysis, Execution Focus, ISO 9001, Persistence and Tenacity, Quality Control (QC), Quality Standards, Quality Systems Documentation, Report Writing, Sample Testing, Technologically Savvy