Manufacturing Analyst, Continuous Improvement

Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all phases of drug development with a mission of improving the lives of patients and medicines essential to people all over the world. Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact, and is critical to our success. With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!Join our mission at Adare!What can Adare offer you?Medical/dental/vision/life - low employee premiums401k with a highly competitive matchGenerous PTO, including floating holidaysCareer growth and internal opportunitiesTuition reimbursementRelocation assistancePerformance-based bonusEmployee Recognition ProgramsWe are seeking to hire a Manufacturing Analyst, Continuous Improvement to join our Manufacturing Support Team...If any of the below describes you, we would love to meet you!JOB SUMMARYThis position supports manufacturing operations by analyzing production data, monitoring key performance metrics, and identifying opportunities for continuous improvement. This role assists with quality deviation investigations, root cause analysis, and operational error tracking to improve right-first-time performance. The Manufacturing Analyst also supports documentation management, internal audits, and compliance initiatives while providing data insights that help drive operational efficiency and reduce risk.ESSENTIAL DUTIES AND RESPONSIBILITIES:Complete trending data for each production batch for future analysis.Assist in monitoring and reporting department metrics on a continual basis.Assists in quality deviation investigations and supports root cause analysis.Develop and maintain a system for monitoring and reporting department metrics on a continual basis. Including a right the first-time matrix to track operational errors and develop recommendations for reduction in errors.Develop and maintain QA trending spreadsheets, review trending for potential issues or future OpEx initiatives.Provide documentation services to the Manufacturing department including writing, revising, formatting, processing, filing, and maintaining documents, including electronic files.Support Production Manager in reducing compliance risk by aiding in performing internal audits and developing action items to correct risks.Support and promote Safety and cGMP programs, ensuring strict conformance to all current FDA and cGMP guidance's and guidelines.Support all Continuous Improvement efforts within the department.Perform other tasks as required.REQUIRED SKILLS AND QUALIFICATIONSBachelor's Degree in Business Administration or a sufficient combination of work experience and training.Ability to perform mathematical calculations.Knowledge of cGMPs compliance.Must be capable of effectively communicating in both oral and written mannerMust be able to provide accurate and affirmative instructions and reports to employees and management.Must be able to organize, plan, and control.Must have flexibility to work any shift or schedule with short notice.Proficient writing and speaking EnglishAdare Pharma is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status.PRINCIPALS ONLYNO AGENCIES OR THIRD PARTIES