Quality Professional

Role: Sr. Quality Professional**Siemens founded the new business unit Siemens Advanta (formerly known as Siemens IoT Services) on April 1, 2019 with its headquarter in Munich, Germany. It has been crafted to unlock the digital future of its clients by offering end-to-end support on their outstanding digitalization journey. Siemens Advanta is a strategic...

Company Overview Well known Prestigious MNC who is a leading manufacturer of trucks buses& construction equipment's. Job Description PMP(Project Management Professional ) This is how you could make an impact As PMP, you would be accountable to lead and manage purchasing activities such as timely sourcing, decide on vendor budget, planning,...

Role:Quality Professional**Siemens founded the new business unit Siemens Advanta (formerly known as Siemens IoT Services) on April 1, 2019 with its headquarter in Munich, Germany. It has been crafted to unlock the digital future of its clients by offering end-to-end support on their outstanding digitalization journey. Siemens Advanta is a strategic advisor...

IntroductionAt IBM, work is more than a job - it's a calling: To build. To design. To code. To consult. To think along with clients and sell. To make markets. To invent. To collaborate. Not just to do something better, but to attempt things you've never thought possible. Are you ready to lead in this new era of technology and solve some of the world's most...

PMP(Project Management Professional )This is how you could make an impact As PMP, you would be accountable to lead and manage purchasing activities such as timely sourcing, decide on vendor budget, planning, quality assurance and risk management into cross-functional product development projects. You will be a key player in the cross-functional product...

PMP(Project Management Professional )This is how you could make an impact As PMP, you would be accountable to lead and manage purchasing activities such as timely sourcing, decide on vendor budget, planning, quality assurance and risk management into cross-functional product development projects. You will be a key player in the cross-functional product...

Job description: Evaluate safety complaint escalations, assess and make decisions on medical device reporting [Medical Device Report (MDR)MedWatch Form 3500A], in accordance with 21 CFR 803, and documenting those decisions. File MDRs when needed and communicate (as appropriate) to the EU Authorized Representative or Regional Unit. Work with members of other...

Department : Operations Quality Consulting & Projects Are you an experienced quality professional looking for a new challenge? Do you thrive in a fast-paced and dynamic environment? We are seeking a Senior Quality Professional to join our team at Novo Nordisk. If you are passionate about ensuring compliance and driving quality excellence, then read on and...

Job Description: Quality Culture: Ensure awareness for quality focus to increase customer satisfaction, particularly in the development process Plan, implement and live Quality culture within Product Line and organization level (Implement the defined processes, improve product quality, initiate process improvements, and drive continuous improvements (CI) in...

Standards and Regulations Good knowledge of the relevant Standards/Regulations for medical device manufacturers (ISO 13485, ISO 14971, MDD, MDR, 510(k) etc.) Ensuring compliance of products as per MI PLM and SHPL QMS requirements Co-ordination with Quality Manager on various SHPL QMS related activities Conducting/participating in Internal Audits and...

Department: SOP Service CenterAre you detail-oriented and passionate about ensuring quality standards? Do you thrive in a dynamic and global team environment? We are looking for an Advanced Quality Professional II to join our Quality GBS department at Novo Nordisk. If you are ready for a challenging and rewarding career, read on and apply today for a...

Evaluate safety complaint escalations, assess and make decisions on medical device reporting [Medical Device Report (MDR)-MedWatch Form 3500A], in accordance with 21 CFR 803, and documenting those decisions. File MDRs when needed and communicate (as appropriate) to the EU Authorized Representative or Regional Unit. Work with members of other teams to review,...

Department: Operations Quality Consulting & Projects Are you an experienced quality professional looking for a new challenge? Do you thrive in a fast-paced and dynamic environment? We are seeking a Senior Quality Professional to join our team at Novo Nordisk. If you are passionate about ensuring compliance and driving quality excellence, then read on and...

Department: SOP Service CenterAre you detail-oriented and passionate about ensuring quality standards? Do you thrive in a dynamic and global team environment? We are looking for an Advanced Quality Professional II to join our Quality GBS department at Novo Nordisk. If you are ready for a challenging and rewarding career, read on and apply today for a...

Department: SOP Service Center Are you detail-oriented and passionate about ensuring quality standards? Do you thrive in a dynamic and global team environment? We are looking for an Advanced Quality Professional I to join our Quality GBS department at Novo Nordisk. If you are ready for a challenging and rewarding career, read on and apply today for a...

The position As a Advanced Quality Professional II, you will Perform writing/editing of standard operating procedures/user guides/work instructions in QualityDocs – adhering to content management system and process. Support to knowledge management and good collaboration with stakeholders and colleagues. Understand the Line of Business requirements...

About the DepartmentNovo Nordisk Quality GBS was established in May 2015. We are responsible for supporting and development of overall quality services, such as training coordination, content control, digital solutions, quality and compliance management and records management for various units within Novo Nordisk.Here, you will be a part of an ambitious,...

The position As an Senior Quality Professional II Master Data, you will have the following responsibilities: Master Data Approval and Coordination: Take a key role in the approval process of Master Data and Engineering Change Orders (ECO) in SAP and Winshuttle systems for all NN products. Ensure accuracy and completeness of data.Master Data Quality...

The opportunityAs Sr. PV professional, ICSR quality, part of ICSR Quality KPIs, reports & metrics Team within the ICSR Quality, KPIs & Metrics sub-function within Patient Safety Operations (PSO), the role in the Global Patient Safety & Pharmacovigilance department within Teva Global R&D (Research & Development) reports to Sr. manager, ICSR Quality KPIs,...

Who we areTogether, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines,...