Novo Nordisk Released Job Openings On 08-12-2021. Novo Nordisk is a leading global healthcare company, founded in 1923 and headquartered in Denmark.Our purpose is to drive change to defeat diabetes and other serious chronic diseases such as obesity and rare blood and endocrine disorders. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease.
Vacancy Details:
Novo Nordisk hiring M.Sc,B.Sc Graduates with 04+ years of relevant experience for Quality Associate Position.Complete Details for the Quality Associate as follows.
Important Details :
- Location : Bengaluru
- No of Vacancies:NA
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application: 08-12-2021
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
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Job Description/Skills Required
As a Quality Associate your main responsibilities will be:
Documentation control and distribution responsible
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- Content responsible for Indian affiliate, Approval, uploading of local procedures in Quality Docs.
- Handling reviews and comments on procedure drafts.
- SOP expert in the affiliate and approve SOP deviations.
- Maintenance and distribution of procedures.
- Product Release Responsible for NN owned products in affiliates.
- Evaluation and release of NN A/S products.
- Release of repackaging batch with review and approve the batch documentation.
Training
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- Induction training of new employees as a part of iACE.
- Affiliate ISOtrain responsible person (training coordinator).
- Ongoing training on applicable procedures.
Repackaging
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- Co-ordinate with distributor and prepare repackaging plan for the products (e.g. Tender Requirements).
- Review and approve the Batch documentation of Repackaging
Change control and Deviations
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- Initiation, implementation, and follow-up for completion of Change Control.
- CR Expert and QA Approver.
- Review and approval of deviations (planned/ unplanned) rose by all departments. Follow-up on action plans and closure within the timelines.
Destruction
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- Review for necessary approvals and document the destruction of NN products, archiving documents.
Validation
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- Review and approval of the validation protocol and report for all the temperature distribution study conducted in the distributor’s sites.
- Review and approval of Periodic system evaluation (PSE) of cold rooms conducted at distributor’s sites.
Quality Control
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- Verify clinical expedited safety reports before reporting to concerned Indian regulatory authorities.
- QC of logging of customer contacts.
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- Overall responsibility of handling the business-critical documents in the affiliate.
- Train and support other departments.
Review Labeling Text Matter (QMR)
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- Review and ensure the Labeling Text Matter are complying with the local and product requirements.Â
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