- 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 Assurance: Plan, coordinate, and execute Quality Assurance (QA) tasks related to Master Data as necessary. This involves ensuring data integrity, consistency, and compliance with regulatory requirements.
- Regulatory Compliance Support: Provide Quality Assurance services specifically tailored for Regulatory Affairs and other pertinent areas within client master data. This includes ensuring adherence to regulatory standards and guidelines.
- Global Labelling Quality Assurance: Oversee quality assurance for global labelling across all NN products. Support or participate in core process groups dedicated to labelling. Ensure labelling compliance and accuracy.
- Training, Audits, and Process Improvement: Provide on-the-job training to colleagues and serve as a mentor or buddy for new hires when necessary. Participate in audits and inspections, contributing to continuous improvement initiatives. Additionally, actively engage in relevant cross-functional quality projects to enhance overall processes and outcomes.
- The candidate should hold a graduate or post-graduate degree in Science or possess a comparable qualification relevant to the pharmaceutical industry.
- Demonstrates 7-10 years of overall work experience within the pharmaceutical sector, with a minimum of 3-5 years focused on SAP systems
- Proficient in PP-PI (Production Planning - Process Industry) and MM (Material Master) modules, with expertise in managing processes such as printed packaging material approvals, BOM approval, MM approval, Batch release, and ECM approvals.
- Proficient in PC-tools with extensive knowledge of MS Office suite. Exhibits excellent presentation skills and possesses advanced knowledge of MS Office, including the ability to analyze data sets and advanced Excel skills.
- Familiarity with quality processes and tools such as Deviation Management, Change Request (CR), Quality Assurance Plan (QAP), Quality Management Review (QMR), and Standard Operating Procedures (SOPs).
- Capable of managing cross-functional project groups across borders and cultures, facilitating effective communication and collaboration.
-
Quality Professional
2 weeks ago
Siemens Bengaluru, India**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 suppor ...
-
Quality Professional
3 weeks ago
Siemens Healthineers Bengaluru, India**Responsibilities**: · - Support the audit program manager in definition and implementation of comprehensive audit programs and audit methodologies to effectively address identified risks · - Interact with stakeholders at all levels in developing comprehensive audit plan and exe ...
-
Quality Professional
1 week ago
Siemens Healthcare Private Limited Bengaluru, India PermanentStandards 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 ...
-
Advanced Quality Professional Ii
2 weeks ago
Novo Nordisk Bengaluru, Karnataka, IndiaAdvanced Quality Professional II - Records Management · **Category**:Quality**Location**:Bangalore, Karnataka, IN**Department**:Novo Nordisk Quality GBS- Records Management Team- · **The position** · - As a Senior Quality Professional at Novo Nordisk, you will:- Provide daily sup ...
-
Advanced Quality Professional Ii
2 weeks ago
Novo Nordisk Bengaluru, IndiaAdvanced Quality Professional II · **Category**:Quality**Location**:Bangalore, Karnataka, IN**Department** - QMS Operations- · **The Position** · - As an Advanced Quality Professional II, you will be responsible for case handling on QualityDocs (a content management system by Vee ...
-
Quality Professional
1 week ago
Siemens Healthcare Private Limited Bengaluru, IndiaStandards 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 requirementsCo-ordination with Quality Manager on various SHPL ...
-
Advanced Quality Professional I
3 weeks ago
Novo Nordisk Bengaluru, India**Department - **QMS Operations · **The Position** · - Perform data corrections in novoGloW. · - Maintaining the master data, master keyword lists and profiles in novoGloW. · - Participate in User Acceptance Test and PQ in novoGloW releases. · - Training and onboarding of new nov ...
-
Bgsw/eqm-ae Quality Professionals
4 weeks ago
Bosch Group Bengaluru, IndiaCompany Description · Bosch Global SW Technologies Private Limited is a 100% owned subsidiary of Robert Bosch GmbH, one of the world's leading global supplier of technology and services, offering end-to-end Engineering, IT and Business Solutions. With over 19,500 associates, it's ...
-
Senior Quality Professional I
5 days ago
Novo Nordisk A/S Bengaluru, IndiaDepartment : 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 ...
-
Senior Quality Professional I
2 weeks ago
Novo Nordisk A/S Bengaluru, IndiaDepartment : 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 passio ...
-
Senior Quality Professional II
3 weeks ago
Novo Nordisk bangalore, IndiaThe 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 a ...
-
Senior Quality Professional I
3 weeks ago
Novo Nordisk Bengaluru, IndiaDepartment: 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 r ...
-
Senior Quality Professional I
2 weeks ago
Novo Nordisk Bengaluru, IndiaDepartment: 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 passion ...
-
Advanced Quality Professional II
3 weeks ago
Novo Nordisk A/S Bengaluru, IndiaDepartment: 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 II to join our Quality GBS department at Novo Nordisk. If you are ...
-
Senior Quality Test Professional
3 weeks ago
Siemens Technology and Services Private Limited Bengaluru, India PermanentHelloVisionary · We empower our people to stayresilient and relevant in a constantly changing world. We're looking for peoplewho are always searching for creative ways to grow and learn. People who wantto make a real impact, now and in the future. Does that sound like you? Then ...
-
Quality Professional
1 week ago
Siemens Mobility Bengaluru, India**Job ID**: · **Company**: · - Siemens Technology and Services Private Limited**Organization**: · - Advanta**Job Family**: · - Quality Management**Experience Level**: · - Experienced Professional**Full Time / Part Time**: · - Full-time**Remote vs Office**: · - Office/Site only**C ...
-
Quality Professional
1 week ago
Siemens Healthineers Bengaluru, IndiaJob 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 appro ...
-
Quality Professional
2 weeks ago
Siemens Healthineers Bengaluru, IndiaEvaluate 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 Aut ...
-
2023 bgsw/eqm-xc-da Quality Professionals
4 weeks ago
Bosch Group Bengaluru, IndiaCompany Description · Robert Bosch Engineering and Business Solutions Private Limited is a 100% owned subsidiary of Robert Bosch GmbH, one of the world's leading global supplier of technology and services, offering end-to-end Engineering, IT and Business Solutions. With over 19,5 ...
-
2024 bgsw/eqm-xc-dx Quality Professionals
2 weeks ago
Bosch Group Bengaluru, IndiaCompany Description · **Bosch Global Software Technologies Private Limited** is a 100% owned subsidiary of Robert Bosch GmbH, one of the world's leading global supplier of technology and services, offering end-to-end Engineering, IT and Business Solutions. With over 22,700 associ ...
Senior Quality Professional II - bangalore, India - Novo Nordisk A/S
![Default job background](https://contents.bebee.com/public/img/bg-user-ex-1.jpg)
Description
Department: R&D Quality GBS, Novo Nordisk Quality GBS
Are you passionate about ensuring high-quality processes and products? Do you have experience in quality assurance and regulatory compliance? We are looking for an Senior Quality Professional II - Master Data to join our R&D Quality team at Novo Nordisk. If you are ready for a challenging and rewarding career, read on and apply today for a life-changing opportunity.
The position
As an Senior Quality Professional II - Master Data, you will have the following responsibilities:
Qualifications
To be successful in this role, we are looking for a candidate with the following qualifications:
About the department
You will be joining our R&D Quality team, which is part of the Development Organization at Novo Nordisk. Our team plays a vital role in supporting the drug and device development process, ensuring high quality and fit-for-purpose processes throughout the entire value chain. We provide quality and compliance support to various areas within the organization, including Regulatory Affairs, Global Safety, Clinical Reporting GBS, and Clinical Data Sciences GBS. Working in a global setting, we focus on delivering viable products that make a difference to patients and ultimately benefit society.