- Catalent (Philadelphia, PA)
- …Supervisor. The Quality Inspector is responsible for process monitoring and auditing of packaging operations, the duties including real-time batch documentation ... in the course of packaging operations. This may require the simultaneous auditing and/or monitoring of one or more operations. Verifies and/or reconciles materials… more
- Catalent (St. Petersburg, FL)
- …degree, preferred; Certified auditor or lead auditor credentials, preferred 5+ years auditing experience Experience working in an auditing role within the ... International Regulations affecting pharmaceutical products and medical devices Sterile/biologic/ATMP/C> auditing experience preferable Working knowledge of industry related guidelines… more
- Catalent (Manassas, VA)
- …, required; Certified auditor or lead auditor credentials, preferre d 5 years+ auditing experience and supervisory experience , required Experience working in an ... auditing role within the Pharmaceutical/Medical Device industry Knowledge and understanding of the following principles and guidelines: EU EudraLex Volume 4 GMPs, 21… more
- BioAgilytix (San Diego, CA)
- …similar organizationMinimum Preferred Qualifications: SkillsInternal and/or external GxP auditing experienceAbility to work in fast-paced environment where multiple ... projects are in process and must be completed in a timely mannerExcellent verbal and written communication skillsAbility to deal effectively with a diversity of individuals at all organizational levelsAcute attention to detailProficiency in Microsoft Office… more
- Merck & Co. (Durham, NC)
- …contracts, supervises work execution, and follows-up on contract work including the auditing of time and material reportsOversee and maintain schedule adherence and ... unplanned calibrations, and maintenance. Troubleshoots equipment and performs necessary repairs Ensure applicable equipment and systems are maintained in a compliant statePerform other tasks as requested by site management to meet the requirements and goals… more
- Catalent (Philadelphia, PA)
- …of FDA cGMP's Ability to quickly learn and implement QA Auditing techniquesKnowledge reading engineering drawing/material specification, a plusIndividual will be ... required to stand and/or sit for long periods of time, occasionally lift 0-15 pounds Why you should join Catalent: Defined career path and annual performance review and feedback process Diverse, inclusive culture 152 hours of PTO + 8 paid holidaysSeveral… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …1271 is required and 600, 601, and 610 is preferred. Experience reviewing/ auditing documentation including but not limited to: Batch Records, SOPs, Work ... Instructions, Validation protocols. Proficient with using Microsoft Office applications (Outlook, Excel, Word, and Powerpoint). Must have flexibility to work on weekends #LI-JK1 #LI-OnsiteLegend Biotech is a proud equal opportunity/affirmative action employer… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …environment with a positive attitude under minimal supervision Experience reviewing/ auditing GMP documentation Strong proficiency with using Microsoft Office ... applications #LI-NPLegend Biotech is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is Legend's policy to ensure equal employment opportunity… more
- BioAgilytix (Durham, NC)
- …similar organizationMinimum Preferred Qualifications - SkillsInternal and/or external GxP auditing experienceAbility to work in fast-paced environment where multiple ... projects are in process and must be completed in a timely mannerExcellent verbal and written communication skillsAbility to deal effectively with a diversity of individuals at all organizational levelsAcute attention to detailProficiency in Microsoft Office… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …of regulatory bodies on pharmaceutical operations. preferred- Experience auditing software vendors is preferred. preferred- International experience preferred; ... at minimum, experience working with diverse cultures and employees is required. Travel Ability to travel up to 10% Travel to Europe, Japan and other DS locations. Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …improvement projects assigned potentially within regulatory compliance, internal/supplier auditing , or customer focus activitiesPerforming the necessary daily ... responsibilities in accordance with current Standard Operating Procedures (SOPs) and GMP regulationsSupport Quality personnel with pharmaceutical investigations to determine root cause and corrective actions.Support inspection readiness activities, including… more
- Insmed Incorporated (Bridgewater, NJ)
- …other staff members to develop additional GVP expertise in quality and auditing resources. Qualifications:Minimum BS degree in Chemistry or related life sciences ... discipline required with minimum 10-15 years of experience, 7 years of which are in Pharmacovigilance.Advanced degree (MS, PhD, MBA) preferred. In lieu of advanced degree, additional years of equivalent experience will be considered.Requires solid experience… more
- St. Luke's Health System (Meridian, ID)
- …management for terminally ill patients in homes. In addition, you will be auditing charts for all admissions and recertifications and tracking orders to ensure ... accuracy and completion. This position allows you to work from home or in the office and requires travel within the Treasure Valley when needed for home visits. The person needs to be able to work autonomously and as a team, have interpersonal and… more
- XPO (E Chillisquaq, PA)
- …all employees reporting to the Service Center, including tracking and auditing employees' hours, handling payroll issues and personnel changes, administering ... corrective action and monitoring the coaching, training, and development of your staff Plan the daily manpower needs to ensure freight is delivered and picked up in a timely manner Provide clear and frequent information to all employees about Service Center… more
- Ingersoll Rand (Southern Pines, NC)
- …daily Inventory and Quality management throughout the Plant to include; counting, auditing , research and data analysis within Receiving, WHS, Shipping, Machining and ... Assembly departments as requiredInvestigate inventory discrepancies, make corrections and ensure appropriate management levels are aware of inventory outcomes and corrective measures are implemented to ensure continuous improvementsResponsible for facility… more
- National Archives and Records Administration (College Park, MD)
- …Records Administration. This position is that of the Assistant Inspector General for Auditing (AIGA), located in the Office of the Inspector General (OIG), Office of ... Audits (OA). The Assistant Inspector General for Auditing (AIGA) provides executive leadership and direction to OIG...audit activities. Responsibilities As an Assistant Inspector General For Auditing , you will: - Be responsible for planning and… more
- ConEdison (New York, NY)
- Project Auditor, Auditing EHS Operations & IT Job Info 112415 Posting Expiration Date:Jun 20, 2024 Schedule Type:Full-Time Minimum Salary:$105000 Maximum ... Salary:$145000 Organization: Auditing Department:EHS Operations and IT Section: AUDITING EHS Operations & IT Location:NY-New York-4 Irving Pl Headquarters Similar… more
- ConEdison (New York, NY)
- Project Specialist - Auditing -2H Job Info 112427 Posting Expiration Date:Jun 30, 2024 Schedule Type:Full-Time Minimum Salary:$105000 Maximum Salary:$145000 ... Organization: Auditing Department:Cust Ops Finance & Procur Section: AUDITING Cust Ops Fin &Procmnt Location:NY-New York-4 Irving Pl Headquarters Similar Jobs… more
- Regeneron Pharmaceuticals (Troy, NY)
- We are currently looking to fill a Manager, Quality Auditing (Post Audit) position. This position is responsible for providing professional expertise, leadership, ... oversight and assisting with planning for the Regeneron Quality Auditing function. Quality (GMP) Auditing is responsible for maintaining the external audit… more
- Regeneron Pharmaceuticals (Troy, NY)
- We are currently looking to fill an Associate Director of Quality Auditing position. This position will be responsible for providing professional expertise, ... leadership, oversight and planning for the Regeneron Quality Auditing function, with primary emphasis on GMP, IT and...that may impact GMP operations and/or product. Quality (GMP) Auditing is responsible for maintaining the internal and external… more
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