11 Qms Systems Jobs

Role & responsibilities 1. Implement effective Plant Quality Management System 2. In case if any problem is detected after dispatch of product, then customer is informed immediately to quarantine Material & necessary action, Monitor Quality & QMS objectives Preferred candidate profile a. Stop the machine if the process is not under control or found any non-conformity in the process b. To stop shipment to correct quality problems on observing non-conformity c. To contain affected batch before it reaches customer d. To delegate personnel in all shifts for meeting requirements of product conformity To communicate employees on Benefits of QMS, Quality Policy, CSR

Role Overview: You will be responsible for performing visual, dimensional, and functional inspections on finished products. Your role will involve verifying compliance with engineering drawings, specifications, and work instructions. You will be using measurement tools such as calipers, micrometers, gauges, CMM reports, and test fixtures. It will be your duty to document inspection results on inspection forms, quality logs, or digital systems (ERP/MES/QMS). Identifying, recording, and reporting nonconforming materials, initiating NCRs, and segregating defective products will also be part of your responsibilities. Additionally, conducting final release checks, ensuring calibration status of t...

**Role Overview:** As an individual contributor at USP, you will be responsible for applying your knowledge and practical experience in executing bioanalytical projects related to collaborative testing of Reference Standards, Analytical Reference Materials, documentary standards, and characterization of various biological products. Additionally, you will actively engage and contribute to verification, international, and national reference standard development programs as assigned. **Key Responsibilities:** - Align with USP's mission, goals, and objectives, and comply with USP's guidelines and requirements. - Demonstrate strong laboratory skills and hands-on expertise in Mass Spectrometry, Ca...

As a Management Consultant in the Life Sciences Strategy & Consulting team, you will be responsible for supporting clients in Quality transformation initiatives. Your expertise in the Quality domain, with exposure to QMS systems, will be invaluable in this role. Key Responsibilities: - Lead or support Quality projects, including process improvement, compliance, and system-related transformations. - Perform functional and technical business analysis by gathering requirements, mapping processes, and documenting workflows. - Analyze and optimize quality processes such as Audits, deviations, CAPAs, root cause analyses, periodic reviews, and audit trail monitoring. - Collaborate with cross-functi...

Role Overview: You will be a hands-on, non-supervisory individual contributor at the U.S. Pharmacopeial Convention (USP), a scientific nonprofit organization setting standards for medicines, food ingredients, and dietary supplements worldwide. Your role will involve executing bioanalytical projects, contributing to the development of reference standards, and engaging in verification programs. Key Responsibilities: - Align with USP's mission, goals, and objectives, complying with guidelines and requirements. - Demonstrate expertise in analytical Chromatography, Biochemical assays, and Enzymatic/Protein assays. - Perform LOD & Water content experiments, plan and execute RS and Assay experiment...

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...