5 jobs found in Oklahoma City, OK

The Senior Manager Accounting will be responsible for management of the Inventory Accounting team based in Limerick in connection with the Company’s biopharmaceutical manufacturing operations in Limerick and International entities. A typical day might include, but is not limited to, the following:  Reporting of monthly actual results for inventory for the international entities Responsible for Profit in Inventory Elimination for international entities Reviewing and handling the company’s inventory and standard cost system including annual standards' development Reviewing and maintaining company’s inventory and standard cost system Oracle Process Manufacturing Working with Master Data Management to ensure production Recipes / BOM’s are accurate and are reflected in the Standard Costing calculations Reviewing Sub Ledger (Production, Inventory, Purchasing, Revaluation, Order Management) Responsible for coordination and review of quarterly inventory...

Are you a seasoned payroll professional with a passion for accuracy and efficiency? Do you thrive in a dynamic, fast-paced environment and have a knack for managing international payrolls? If so, Regeneron is looking for you! As an Associate Manager, you will play a crucial role in ensuring our payroll processes run smoothly and accurately across multiple countries. Your expertise will be instrumental in driving process improvements, managing a team of payroll analysts, and collaborating with various departments to support our growing global operations. A Typical Day Might Include: Ensuring Payroll Accuracy: Oversee and review the work of payroll analysts, ensuring all inputs are accurate before submission to external payroll providers. This includes: - Running payroll reports from Workday and cross-referencing with inputs - Verifying data from various departments (fleet, benefits, equity, etc.) Quality Assurance: Confirm that payroll analysts' reconciliations are...

Summary: Responsible for assisting management with ensuring auditors have the education, experience and/or training necessary to be able to perform audits, and assisting with the maintenance and continuous improvement of the auditor training program. Responsible for planning, coordinating and performing pre-, during and post-audit activities for assigned audits. Extensive knowledge of USA and EU GxP regulations is required. Essential Duties and Responsibilities include, but are not limited to, the following: Maintain professional expertise and knowledge of audit criteria including, but not limited to, internal company policies and procedures, and applicable local and international regulations, standards and guidelines (e.g., Chapter 21 of the Code of Federal Regulations, Eudralex Volume 4 and associated Annexes, ISO Standards, and ICH, WHO and IPEC Guidelines, etc.); Monitor industry trends with respect to regulatory agency findings, expectations and warning letters;...

Within this role you will be responsible for planning, coordinating and performing pre-, during and post-audit activities for assigned audits. You will be responsible for assessing systems, processes, procedures and records against applicable U.S. and ex-U.S. GxP regulations, with primary emphasis on GMP, IT and Quality audits that may impact Regeneron operations and/or product. Note this position requires approximately 50% travel globally. As a GMP Quality Auditor, a typical day might include, but is not limited to, the following:   Maintaining professional expertise and knowledge of audit criteria including internal company policies and procedures, and applicable local and international regulations, standards and guidelines (e.g., Chapter 21 of the Code of Federal Regulations, Eudralex Volume 4 and associated Annexes, ISO Standards, and ICH, WHO and IPEC Guidelines, etc.) Supervising industry trends with respect to regulatory agency findings, expectations and...

As a GMP Quality Auditor you will be r esponsible for planning, coordinating and performing pre, during and post-audit activities for assigned audits. You will be responsible for assessing systems, processes, procedures and records against applicable U.S. and ex-U.S. GxP regulations, with primary emphasis on GMP, IT and quality audits that may impact Regeneron operations and/or product. A typical day might include, but is not limited to, the following:   Maintaining professional expertise and knowledge of audit criteria including, but not limited to, internal company policies and procedures, and applicable local and international regulations, standards and guidelines (e.g., Chapter 21 of the Code of Federal Regulations, Eudralex Volume 4 and associated Annexes, ISO Standards, and ICH, WHO and IPEC Guidelines, etc.) Supervising industry trends with respect to regulatory agency findings, expectations and warning letters Performing supplier/external audits and...