6 Qms Systems Jobs

Role Overview: You will be responsible for managing store operations related to Raw Material (RM) and Packaging Material (PM) stores. This includes ensuring proper material handling, labeling, storage, and retrieval as per SOP. You will supervise the inward and outward movement of materials and coordinate dispatch activities. Additionally, you will monitor inventory levels, conduct stock verifications, and coordinate with purchase and production teams for material availability. Key Responsibilities: - Manage overall operations of Raw Material (RM) and Packaging Material (PM) stores - Ensure proper material handling, labeling, storage, and retrieval as per SOP - Supervise inward and outward m...

As a Senior Scientist I or Scientist IV at U.S. Pharmacopeial Convention (USP), you will have the opportunity to contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. Your role will involve aligning with USP's mission, goals, and objectives, complying with guidelines, and demonstrating laboratory skills in various analytical techniques such as Chromatography, SEC-MALS, LC-MS, HPLC/UPLC, Ion-chromatography, Capillary Electrophoresis, and more. You will be responsible for planning and executing Compendial and R&D projects, including proof of concept studies in Biologics ...

1. Job Summary The Production Head is a strategic and hands-on leadership role responsible for overseeing the entire manufacturing process within the rubber plant. This includes planning, coordinating, and directing all activities on the production floor to ensure the efficient, safe, and cost-effective manufacture of high-quality rubber products. 2. Key Responsibilities A. Strategic Planning & Operations Management: Develop and execute production plans and schedules to meet sales forecasts and customer delivery commitments. Allocate resources effectively (manpower, machinery, materials) to maximize output and efficiency. Set and monitor key performance indicators (KPIs) for the production d...

Role Overview: As a Block Head at our injectable manufacturing facility, you will lead a key production block. Your main responsibilities will involve overseeing end-to-end manufacturing operations, managing a team of production staff, driving process optimization, ensuring regulatory audit readiness, maintaining compliance with cGMP standards, implementing changes, overseeing equipment and maintenance, coordinating cross-functionally, and managing inventory and resources. Key Responsibilities: - Oversee end-to-end manufacturing operations - Manage a team of production staff - Drive process optimization - Ensure regulatory audit readiness - Maintain compliance with cGMP standards - Implement...

At USP, inclusive scientific collaboration is highly valued as it is believed that diverse expertise enhances the development of trusted public health standards. The organizational culture at USP promotes equitable access to mentorship, professional development, and leadership opportunities to ensure broad participation in scientific leadership for stronger and more impactful outcomes in global health. As an equal employment opportunity employer (EEOE), USP is committed to fair, merit-based selection processes that allow the best scientific minds, regardless of background, to contribute to advancing public health solutions worldwide. Accommodations are provided to individuals with disabiliti...

As a PMO Lead specializing in Tool Validation & QMS Automation, you will be responsible for driving tool validation projects, automating validation processes, QMS documentation automation, and exploring productivity-enhancing tools in the Engineering Operations of the Digital Unit. Your role is pivotal in ensuring compliance with regulatory standards such as FDA, ISO 13485, IEC 62304, and IEC 82304-1 while promoting innovation and operational efficiency within engineering and quality processes. Your key responsibilities will include owning and managing the lifecycle of tool validation projects, developing and maintaining validation plans, protocols, and summary reports, implementing automate...