QC Chemistry Scientist (2nd shift)

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 jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Quality Job Sub Function: Quality Control Job Category: Professional All Job Posting Locations: Gurabo, Puerto Rico, United States of America Job Description: About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine We are searching for the best talent for a QC Chemistry Scientist (2nd shift) to be located at Gurabo, PR. The QC Chemistry Scientist is responsible for performing and reviewing all chemical and physical testing of raw materials, bulk and finished products, and utilities (i.e., water, etc.) in accordance with internal and compendia specifications. This involves conducting thorough testing to ensure that all products meet established quality standards. In addition to testing, the QC Chemistry Scientist participates in investigations whenever questionable analytical results are generated. This investigative aspect is crucial for identifying and addressing any deviations from expected results, ensuring the integrity of the testing process. Also operates and maintains laboratory instrumentation following established methods and procedures. Prepares testing solutions and samples and accurately documents all raw data in compliance with Good Documentation Practices. Maintaining complete and accurate records is essential for traceability and accountability in the laboratory environment. Additionally, the QC Chemistry Scientist undergoes training on methods and procedures and may perform any special tasks assigned by QC Management in support of the Order Release Department. This ongoing training ensures that the scientist is up to date with the latest techniques and regulatory requirements. Finally, must ensure compliance with all quality control policies, procedures, and systems to facilitate the timely release of high-quality products and support the supply chain process. It is important to note that failure to perform these functions effectively may result in product recall, production delays, and/or back-order status.

Perform laboratory analysis and activities in accordance with cGMP practices, internal and external regulations, and supply chain cycle time goals. Follow laboratory priority report and in-process boards to support manufacturing rhythm wheels and business rules. Comply with laboratory schedules for raw materials and drug product testing and special projects. Adhere to QC initiatives and requirements. Verify documentation of data generated by other QC scientists in a timely manner and according to specifications. Ensure correctness and inform supervisors and managers of any encountered deviations for proper investigation and corrective action plan. Maintain all tested solutions and samples until lot release for any necessary laboratory investigation. Operate laboratory