... timelines. Documentation & Compliance - Review SOPs, protocols, reports, and quality documents. - Ensure compliance with GDP (Good Documentation Practices). - Maintain QMS records in electronic systems. Training & Awareness - Conduct QMS awareness and GMP training programs. - Support employees in understanding quality systems requirements ...
... and regulatory compliance in a medical device manufacturing environment. Requirements - Assist in implementation and maintenance of Quality Management System (QMS). - Support preparation, review, and control of SOPs, formats, and QA documents. - Ensure Good Documentation Practices (GDP) across departments. - Review Batch ...
... stage of our development, with the opportunity to contribute to both our business and the patients we ultimately serve. The Opportunity We are looking for an Executive, Quality Systems to help maintain and continuously improve our Quality Management System (QMS), keeping us compliant with GxP requirements, regulatory standards ...
Job Title: Sr Executive / EHS (M12 grade) Department: Gyproc Wada plant Reports to: EHS Manager -Wada Plant Overview : To cater the requirements of Environmental & Health safety, the dedicated person needed to track, implement and guide on EHS matters in plants. Duties and Responsibilities : - The EHS Executive will be ...
... accessible. If you are passionate about driving quality excellence on a global scale, this is an opportunity to make a meaningful impact at Novartis. As Global QMS Manager, you will drive compliance, innovation, and continuous improvement across critical quality processes that support product release worldwide. Working with ...
... Demonstrated experience building and implementing a QMS is more important. What Success Looks Like First 30 days · Complete the AS9100 gap assessment. · Establish the QMS architecture and document-control framework. · Implement basic material traceability, NCR and production-quality controls. First 90 days · Core QMS processes ...
... of experience as a Business Analyst in IT projects within regulated environments, with at least 3–5 years in a leadership capacity. - Strong understanding of QMS/ Safety/ Regulatory/ Clinical processes and how these are structured into workflows within Veeva Vault applications (Quality Suite/ Safety Suite/ RIM Suite/ Clinical) ...
... G.A.P. Certification Audits • Plan, conduct, and report GLOBALG.A.P. certification, recertification, extension, and other applicable audits. • Conduct GLOBALG.A.P. QMS audits for Option 2 producer groups and Option 1 multisite producers with QMS. • Ensure audit activities are conducted in accordance with applicable GLOBALG.A.P. ...
Job Description EEMEAI Presales Enablement specialist (Junior) Job Description Key Accountabilities NielsenIQ SA&I team is seeking a talented Pre-Sales enablement associate to play a key role in enabling sales teams to be more efficient and stay focused on winning business.
Corporate Sales Executive Start Date Starts Immediately CTC (ANNUAL) ₹ 2,40,001 - 3,00,003 ₹ 2,40,001 - 3,00,003 /year Experience 1 year(s) 1 year(s) Apply By 18 Oct' 26 Posted 3 weeks ago Job Be an early applicant About the job The Manager - Technical Sales will be responsible for driving business growth, developing key ...