Quality Inspector, QC, IQC, QA

Job Summary The Quality Inspector role is to support manufacturing quality. Responsible for timely and effective GMP review of production records in order to maintain a continuous flow of records, and to manage and control materials used for the product realization including nonconforming materials. Responsible for Lot release testing. Job Description Maintain the effectiveness of Quality Management Systems to assure compliance with GMP: Manufacturing site Policies and Procedures

ISO 13485 QMS, 21 CFR 820 QSR

Relevant global quality systems. Participates in the implementation of the Quality Management System. Perform manufacturing QC processes in a timely manner including lot release testing and testing related to validation, qualification. Calibration and maintenance of laboratory equipment and related systems, maintenance of laboratory equipment. Assist in the development of QC/QA procedures, Protocols, reports, create and maintain QC/QA documentation for new and existing products, processes, and equipment. Reviews, interprets, and evaluates analytical data, including raw data, of developmental, clinical, and commercial related products for accuracy and compliance within procedures and GxP requirements. Monitors stability studies of developmental, clinical, and commercial related products tested internal or contract laboratories. Analyze and evaluate preliminary testing data, initiate NCMR and other quality related tasks as appropriate. Assist supervisor/manager in maintaining the current laboratory and QC/QA activities. Contact point for instrumentation issues and providing training and troubleshooting support to the laboratory on new or existing instrumentation. Monitor and ensure compliance of all laboratory equipment and associated systems and provide training to technicians as required. Prepare, review & approve laboratory documentation related to laboratory instrumentation and systems (e.g. SOPs, validation protocols, reports etc.) Provide support to laboratory investigations involving laboratory systems including NCMR and deviation Work with cross functional teams on new product transfer, qualification, validation, etc. Reviews, enters, and maintains stability data for developmental, clinical, and commercial products. Transfers analytical methods and qualification as applicable. Prepares and maintains QC/QA documentation, including protocols, reports, and test methods. Procures reference materials for contract analytical laboratories. Maintains and updates department documents required for regulatory compliance and assures testing requirements adherence to latest regulatory standards. Engage in managing the documentation Change Control Process including receiving / generating, identifying, distributing, tracking, and publishing Change Requests and Orders as applicable. Engage in filing, identification, archiving, storage, recovery and destruction of QC/QA Documentation and Records as needed. Review & Release of WIP Materials and Finished Goods for GMP this includes review of quality records for: Good Documentation Practices/Data Integrity Completeness of records Accuracy of records Lot/part/description accuracy Materials and Finished Goods included, but not limited to: Wafers HPC Preparation, and performing a variety of routine and QC/QA tasks following cGMP regulations Work collaboratively with required functions as part of a cross functional team to investigate customer complaints and address them in a timely manner. Work collaboratively with cross functional teams as relevant and ensure that Change controls, deviations/investigations, CAPAs are initiated and executed as applicable in a timely manner. Qualifications Required Knowledge of GMP (21 CFR Part 820, and ISO 13485) Hands‑on knowledge of computer applications including use of the Internet, Word and Excel applications and presentation software such as Power Point Sound knowledge of cGMP and experience in a regulated industry Strong verbal and written communication skills Excellent organizational skills along with strong attention to detail Education / Experience HS degree is preferable or equivalent 2-3 years of experience in an FDA regulated industry (Biotech, Pharma or Medical Device manufacturing) with Quality Assurance role Experience with developing/documenting procedures/work instructions Familiar with a variety of the field’s concepts, practices, and procedures Working knowledge of computerized quality systems (i.e. QMS, LIMS) is a plus Demonstrated change management experience, guiding the organization to the desired state Preferred Experience with Electronic Systems for handling complaints, investigations, CAPAs, Calibrations, Electronic Batch records, control of documents etc. Competencies Accountability for Results - Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change. Strategic Thinking & Problem Solving - Make decisions considering the long‑term impact to customers, patients, employees, and the business. Patient & Customer Centricity - Maintain an ongoing focus on the needs of our customers and/or key stakeholders. Impactful Communication - Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results. Respectful Collaboration - Seek and value others’ perspectives and strive for diverse partnerships to enhance work toward common goals. Empowered Development - Play an active role in professional development as a business imperative. Benefits Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short‑term and long‑term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits. Compensation Minimum $36.00 - Maximum $48.30, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate’s job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws. Disclaimer This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary. Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic. If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting the accommodation request department. Come discover more about Otsuka and our benefit offerings. #J-18808-Ljbffr Dormont Manufacturing Company