Position Overview The Quality Assurance (QA) Analyst III, under minimal direction, will be responsible for review and/or approval of basic and technical documentation, drafting and reviewing of internal Quality policies and procedures, performing product related activities, performing Quality audit functions, performing product release activities, identifying process and Quality System improvements, and acting as a QA liaison internally and externally. Job Description Reports to: Director, Quality Assurance/Senior Manager, Quality Assurance Work Location: College Station, TX (On-site at NCTM building) Primary Responsibilities Review and/or approve basic and technical documentation with minimal supervisory oversight to include, but not limited to: Standard Operating Procedures Batch Production Records (completed and approval) Commissioning, qualification and validation protocols and reports Deviation Reports Corrective Action/Preventive Action Plans Technical data review and approval QC data review and approval Drug Substance/Product Reports Trending QA data Draft and review internal Quality policies, procedures, and reports. Perform inspection of final product containers and review and/or approval of executed process records and data. Perform Quality audit functions to include, but not limited to: Audit of lab notebooks Audit of equipment logbooks Review of vendor, supplier, contract laboratory audit questionnaires Lead vendor, supplier, contract laboratory and client audits Identify process and Quality System improvement opportunities. Provide daily guidance for the compliance of the QA department to national and international standards and regulations. Support Regulatory, client, and internal audits. Act as QA liaison to internal Departments and external Client Quality Groups and Vendor/Contract Laboratory Quality Groups. Promptly notify Senior Management of potential quality or regulatory issues that may affect product quality or regulatory compliance. Assist with technical oversight/training for the QA team. Assist with compliance related functions. All other duties as assigned. Qualifications Master’s Degree and 1+ years’ experience in Pharmaceutical or other regulated industry. Bachelor’s degree and 3+ years’ experience in Pharmaceutical or other regulated industry. Associates Degree and 5+ years’ experience in Pharmaceutical or other regulated industry. High school or equivalent and 8+ years’ experience in Pharmaceutical or other regulated industry. Certified Quality Auditor preferred. Degree in Biology or Chemistry preferred. Excellent written and oral communication skills. Excellent organizational, analytical, data review and report writing skills. Ability to set personal performance goals and provide input to departmental objectives. Ability to multitask and easily prioritize your work. Ability to work independently with little supervision. Proficient in Microsoft Excel, Word and PowerPoint. All candidates must have a working knowledge of cGMP regulations for the production of drug, biologics or vaccine products. Role model for company core values of trust, delighting our customers, and Gemba. Physical Requirements The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to: Experience prolonged standing, some bending, stooping, and stretching. Lifting up to 25 pounds on occasion. Use hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment is required. Attendance is mandatory. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBTHR@fujifilm.com or (979) 431-3500). #J-18808-Ljbffr
...A language service provider in Hicksville, NY is seeking Greek interpreters to facilitate communication for the Limited English Proficient community. Interpreters will ensure adherence to professional standards and maintain confidentiality while providing services in various...
...serious training, where they work alongside former pro and D1 athletes coaching them at the highest standard. We are hiring a Virtual Assistant to own our billing operations. This is a focused role centered on invoicing, payment tracking, and family billing...
...insertion based on client anatomy and condition Utilize complementary modalities as appropriate, which may include: Cupping therapy Moxibustion Gua sha Acupressure, shiatsu, or tuina Heat and/or cold therapies Ayurvedic Counseling Perform comprehensive...
...Were different than most primary care providers. Were rapidly expanding and we need great people to join our team. The Care Promoter 1 is an unlicensed medical professional cross-trained to perform routine administrative and clinical tasks to keep the medical centers...
Job ID: 16469 Core Responsibilities Pay Rate: $20 to $25 Assembly & Soldering: Read blueprints, wiring diagrams, and schematics to mount, connect, and secure electronic parts (resistors, microchips, etc.) onto circuit boards or larger casings. Use soldering equipment...