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In bgsw quality Professional Template in
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Novo Nordisk Bengaluru, IndiaDepartment: 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 ...
Advanced Quality Professional II - Bengaluru, India - Novo Nordisk A/S
Description
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 II to join our Quality GBS department at Novo Nordisk.
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 clearly and deliver on the agreed timelines.Work and activities performed in this role has significant influence /impact on business and quality error might lead to compliance issues.
Therefore, precision, quality and accuracy are imperative. Ensure KPI targets are met for self and team. On a regular basis, prepare and deliver KPI reports. Act independently and ensure assigned tasks/projects are well planned and executed with strong sense of ownership. Furthermore, you will be accountable to-Ensure that there is a proper back-up for all the tasks assigned, as needed.Ensure regular and proactive communication with stakeholders.
Identify and report potential compliance risks and provide recommendations to mitigate.
Maintain contact with both potential and existing stakeholders in a professional and positive manner.
You will support to knowledge management and good collaboration with stakeholders and colleagues.
In addition to the above, you will contribute to ongoing improvements in cross-functional and global collaboration and share best practices and knowledge.
QualificationsTo be successful in this role, we are looking for candidates with the following qualifications:
Bachelor's or Master's degree in English.
3 to 6 years of experience in Content writing, editing, proof reading etc from Corporate background.
Highly proficient in MS Word, PowerPoint, Adobe Acrobat, Picture/image handling programs- Ex- SnagIt, GIMP.
Experience or knowledge within the pharmaceutical industry is preferred.
Experience working with different cultures and good stakeholder management
Basic Project Management skills.
Excellent oral and written communication, interpersonal skills.
Proactive, self- motivated and team player.
Being responsible and reliable.
Being curious, eager to learn and detail-oriented.
About the department
The Senior Quality Professional I role is part of the SSC (SOP Service Center) department, which offers comprehensive editorial services and solutions in the QualityDocs system (Quality Management System).
Our team of skilled editors provides support for multiple creative content writing and technical writing projects, enhancing the quality of documents and standard operating procedures.
We are also expanding our services to include translation services for SOPs, further augmenting our value-add to the organization.