Technical Writer in Quality Content and Records Management

Zoek Pin Bengaluru, Karnataka


Permanent (Full time)

Recently Posted

“Writing, Editing, Proofreading. Do these words pique your interest? Then, you have the perfect opportunity to put your skills to the test. We are on the lookout for an experienced and self-motivated individual to generate high-quality technical documentation/SOPs. Read the job description below to find out whether your talent aligns with our expectations.” About the department SOP Service Centre is one of the sub-units under Quality Content and Records Management in Novo Nordisk Quality GBS. This team offers comprehensive editorial services and solutions in QualityDocs System to different Line of Business across Novo Nordisk globally while adhering to Quality Management system and NN policies. The position As a Advanced Quality Professional, you will be accountable to- 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 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 Qualifications/Expectations Bachelor’s or Master’s degree in English 3 to 4 years of experience in Content writing, editing, proof reading etc from Corporate background (mandate) Highly proficient in MS Word, PowerPoint, Adobe Acrobat, Picture/image handling programs- Ex- SnagIt, GIMP Experience or knowledge within the pharmaceutical industry is preferredExperience working with different cultures and good stakeholder managementBasic Project Management skillsExcellent oral and written communication, interpersonal skills Proactive, self- motivated and team player Being responsible and reliable Being curious, eager to learn and detail-oriented

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