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:** 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 QC Senior Scientist Investigations to be located in Gurabo, PR.** **Purpose** : Responsible for performing CAPA investigations identified in the Quality Control (QC) area, including, but not limited to, suspect test results for Out of Trend (OOT), Out of Specifications (OOS) and Out of Limit / Level events, and supplier related investigations for chemical, microbiological and physical testing of raw materials, drug products, intermediaries and utilities (i.e. water, etc.) according with internal and compendia specifications. Assures the compliance to all QC policies, procedures and systems to ensure the timely release of high-quality products in support to the supply chain process. Knowledgeable of analytical and microbiological tests performed at the QC area. Serves as back-up of the QC Lab Services supervisor in different forum pertaining to the CAPA process. **You will be responsible for** **:** + Leads CAPA investigations and acts as record owner. + Participation in multidisciplinary meetings to evaluate events that may need to be investigated and provide status of investigation records. + Completes risk assessment following current CAPA procedures. + Investigates and completes the record stages on a timely manner. + Provides rationale to proceed with the usage of the product/ lot/ material. + Performs root cause analysis using applicable tools to identify the immediate cause or root cause of the event, as applicable based on the investigation level and impact category. + Completes the investigation record in accordance to local and global procedures and enforces the on-time closure of records. + Acts as owner of CAPA system records, such as Corrections and CAPA actions. + Performs evaluations and acts as responsible for the completion of risk assessments and documents generation and revisions to support QC operations. + Knowledgeable of the operation of laboratory equipment required for QC chemical and microbiological tests. + Participate in the internal and external forums as QC representative to support base business. + Actively participates in projects, safety and environmental, GMPs, SOPs trainings and others as required and/or special activities that the company promotes to foster employee involvement and their professional development/growth such as environmental/safety/GMP improvement project to simplify, reduce, minimize or eliminate environmental or compliance aspects at the job area. + Actively participates in the generation and analysis of QC performance metrics. + Supports Quality Control Laboratory Internal and External Audits and Inspections. + Supports personnel training. + Temporarily supervisor activities to re-place the supervisor during leave licenses. **Qualifications / Requirements:** + Bachelor’s degree in Sciences is required, Master’s degree is preferred. + A minimum of 2 years of experience in laboratory investigations is required. + Certification in the management of CAPA investigations is preferred. + Certification in Root Cause Analysis tools is preferred. + Knowledge of cGMP’s and compliance is required. + Statistical Analysis Experience using Microsoft Excel, Minitab etc. software is preferred. + Computer and Software skills is required. + LIMS system basic knowledge is preferred. + Technical knowledge of Chemistry and Microbiology is required. + Knowledge of basic sample preparation techniques is preferred. + General knowledge of USP/EP/JP/ChP/ACS compendia general methods and techniques is preferred. + Knowledge of techniques such as HPLC, GC, UV-Visible spectrophotometer, FTIR, TOC, wet chemistry, culturing, biochemical, microscopy, sterility, endotoxin and environmental monitoring is preferred. + Understand impact of laboratory performance on supply chain and business results is required. + Bilingual (English & Spanish) is required. + Availability to work overtime and weekends is required. + Availability to travel up to 10% is required. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson and 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, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource. \#LI-Hybrid