Head Quality And Regulatory - Bengaluru

What can you expect as a FedEx team member? · Career Mobility and Development: When you join FedEx, you're joining a team with possibilities that literally span the world—from opportunities for advancement and location transfer, to training and leadership programs. · Total Compen ...

This is a full-time on-site role for a Quality Analyst and Regulatory Affairs professional located in Bengaluru. · The responsibilities include ensuring product quality by conducting rigorous quality control and assurance processes performing compliance checks and maintaining qua ...

Fourth Frontier es una empresa de tecnología sanitaria en vanguardia que está transformando cómo las personas monitorean y gestionan su salud cardíaca. · ...

We are seeking a highly organized and detail-oriented Quality and Regulatory Specialist to support the ongoing operation and improvement of medical devices Quality Management System (QMS). · Maintain the QMS to ensure the efficiency of the document control process and compliance ...

"Please note that the Job will close at 12am on Posting Close date, so please submit your application prior to the Close Date" · What You Will Do · The Healthcare Quality & Regulatory Compliance Advisor will be responsible for ensuring that all organizational operations, within t ...

This role will support and execute Quality Assurance and Regulatory Affairs activities to ensure compliance with global medical device regulations and effective operation of the Quality Management System (QMS) · ...

We are seeking a detail-oriented and proactive Quality & Regulatory Affairs (QARA) Associate to support the implementation and maintenance of our Quality Management System (QMS) and regulatory compliance for medical devices. · ...

+We are looking for a highly detail-oriented Quality & Regulatory Intern to help us set up and document an FDA-compliant Quality Management System (QMS) from the ground up. · +Setting up anFDA-compliant QMS structure on Google DriveDrafting and organizing QMS documents & SOPs wit ...

Nazwa biura: India - Karnataka - BengaluruGSK to globalna firma biofarmaceutyczna, której celem jest łączenie nauki, technologii i talentów, aby wspólnie wyprzedzać choroby. · ...

Oto krótki opis tego stanowiska: · Zapewniamy elastyczne środowisko pracy. W roli Senior Manažera będziesz odpowiedzialny za zapewnianie wsparcia klientom poprzez dostarczenie im produktów i usług w terminie. Będziesz również odpowiedzialny za zarządzanie zespołem oraz rozwiązywa ...

- Perform operational activities for assigned elements of the regulatory information management process, XEVMPD, and the Global Product Registration List in accordance with quality control and quality improvement methodologies. · - Act as a Data Steward for assigned regulatory da ...

About Us · Redica Systems is a data and analytics SaaS platform that helps regulated industries improve their quality and stay on top of evolving regulations. We are shaping the future of predictive quality with our pioneering work in AI workflows and the development of an exclus ...

· Job Description: · POSITION TITLE: Senior QA/RA Specialist · JOB LOCATION: Bangalore,India · DEPARTMENT: Quality & Regulatory · REQUIRED EDUCATION: Bachelor's degree in biomedical engineering discipline or equivalent · engineering degree · KEY RESPONSIBILITIES: ➢ Product QA/RA ...

Working knowledge of relevant global medical device regulations, requirements, and standards, such as ISO 13485, 21 CFR Parts 803, 806, and 820, ISO 14971, the European Medical Device Directive (93/42/EEC), and EU MDR (2017/745). · Provide Quality and Regulatory Affairs input to ...

Job Description:The Job Holder provides support to GRA Labelling staff, Regulatory Matrix Teams and Local Operating Companies to ensure the timely update, management and communication of quality regional/country Product Information (PI)/labelling and supporting documentation. The ...

Responsible person : Serve as the responsible person (Technical Staff) for all QA-related deliverables at the site, ensuring compliance with standard operating procedures (SOPs). · QMS Implementation & Maintenance : Oversee the implementation and continuous improvement of the Qua ...

We are seeking highly skilled and experienced Life Sciences Regulatory Affairs (RA) Team Leader to join our LS Practice team. The successful candidate will be responsible for LS Regulatory Authoring and/or other assigned RA activities. This leadership role oversees a team of regu ...

Job Title: Inspection Coordinator · ...

Support for regulatory activities including documentation and submissions. · ...

Lead and manage Quality Assurance functions with over 10 years of experience, including 5+ years in leadership roles. · Implement and maintain Food Safety Management Systems (FSMS) ensuring compliance with HACCP, GMP, and GHP standards. · Conduct internal and external audits to a ...