Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility. Responsible for preparation and review of protocols and reports based on the requirements. Responsible for document management and preparation like BMR’s,
Company Overview Zoetis is a global animal health company dedicated to supporting customers and their businesses. With more than 60 years of experience, we deliver quality medicines, biopharmaceuticals, vaccines, diagnostic products, and genetic tests, complemented by
Job TitleQMS Specialist - MRI Job Description Job title: QMS Specialist - MRI Your role: The QMS Specialist is responsible for overseeing QMS processes to ensure an efficient and compliant MR QMS, working under limited supervision. The role analyzes QMS processes
Sr. QMS Manager – Quality & Digital Systems: Position summary: The Sr. QMS Manager – Quality & Digital Systems plays a key role in shaping, maintaining, and continuously enhancing the global Quality Management System (QMS) for medical devices across
Project Role : Custom Software Engineer Project Role Description : Develop custom software solutions to design, code, and enhance components across systems or applications. Use modern frameworks and agile practices to deliver scalable, high-performing solutions tailored
Forvia, a sustainable mobility technology leader We pioneer technology for mobility experience that matter to people. Your mission, roles and responsibilities The main missions of the role are: Perform engineering assignments as part of design /
Forvia, a sustainable mobility technology leader We pioneer technology for mobility experience that matter to people. Your mission, roles and responsibilities The main missions of the role are: Perform engineering assignments as part of design /
Forvia, a sustainable mobility technology leader We pioneer technology for mobility experience that matter to people. Your mission, roles and responsibilities The main missions of the role are: Perform engineering assignments as part of design /
Forvia, a sustainable mobility technology leader We pioneer technology for mobility experience that matter to people. Your mission, roles and responsibilities The main missions of the role are: Perform engineering assignments as part of design /
Description: Responsible to perform sterility testing, bacterial endotoxins testing, LBPC and bioburden testing of raw material, in-process, packing material, finished products, Stability samples and other miscellaneous samples 2. Responsible for water and pure steam sampling and
Description: To ensure compliance with cGLP regulations by analysis and calibration of all aspects of Quality Control at the manufacturing site Essential Functions: To be responsible for Analysis and Calibrations of Quality Control Laboratory instruments. To
Responsibilities & Key Deliverables Lead and Monitor Supplier Process audits, Improvements and VPPAP of Mechanical / Hydraulics Proprietary components (Ex. Aux valve, HSU, Power steering, hydraulics pump, etc.Lead the Improvement of Quality Performance of assigned Suppliers
We are looking for a Quality Assurance & Regulatory Affairs (QARA) professional with 1–3 years of experience in the medical device industry. The candidate will support the maintenance of the Quality Management System (QMS), regulatory documentation, technical
Your Career. Your Impact. Your Future. At Gentherm, we believe the next big breakthrough begins with you. As a global leader in thermal management and pneumatic comfort technologies, we develop advanced systems that deliver meaningful solutions
Creating passion: your responsibilities Roles & Responsibilities: OEM Business • Act as the primary technical interface for major OEM customers (Enercon, Nordex, GE Vernova, Vestas, SGRE). • Manage and resolve customer inquiries related to design, quality,
Carry out preventive, breakdown, and planned maintenance of OSD production equipment, including RMG, FBD/FBP, High‑Shear Blenders Multi‑mill, Co‑mill, Sifter Tablet Compression Machines Capsule Filling Machines Coating Machines (Auto/Perforated Pan) Electrical troubleshooting of: HMI, PLC I/O cards,
Description: Responsible for managing the Quality Management System (QMS), including deviations, OOS/OOAL investigations, CAPA, change control, and ensuring compliance with cGMP and regulatory requirements. Handle audits (regulatory, customer, internal), drive SOP/document control, training systems, and ensure continuous quality
John Cockerill, enablers of opportunities Driven since 1817 by the entrepreneurial spirit and thirst for innovation of its founder, the John Cockerill Group develops large-scale technological solutions to meet the needs of its time: facilitating access
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
Line of ServiceAdvisory Industry/SectorNot Applicable SpecialismDeals Management LevelAssociate Job Description & SummaryAt PwC, our people in audit and assurance focus on providing independent and objective assessments of financial statements, internal controls, and other assurable information enhancing