Work as a Team Member - Quality Assurance @ Mylan
At Mylan, we mean it when we say we work every day to provide access to high quality medicines to the world’s 7 billion people. If you are unconventional, relentless and passionate. If you believe in doing what’s right, not what’s easy. If you are a doer and have a passion for serving others, we want to talk to you.
Make a Difference
At Mylan, each person has the ability to make a difference. From the providers who sell and market our products to the producers who develop and manufacture them and finally to our business partners who support the providers and producers, we all have a mission critical role. Here’s how this role will help:
Prepare controlled documents; Conduct distribution, retrieval, archival and destruction of controlled documents; Prepare new documents as per cGMP requirement, as and when required.
Prepare employee training curriculum, annual schedules; Coordinate with internal trainers and execute the training as per schedule; Maintain, check and update the training records; Assess the training evaluation questionnaires; Conclusion of re-training requirements
Track and highlight deviations in manufacturing operations to the supervisor; Provide line clearances after satisafactory review;
FDF: Perform in-process sampling as per production schedule
Initiate the change control with necessary document support; Execute the approved changes as per the action plan; Prepare the validation protocols and reports; Verify documents with current equipment capability; Execute the validation/ qualification processes at each stage of manufacturing
Prepare and update the vendor list as per the schedule; Initiate the vendor evaluation documents; Maintenance of master data SAP related to vendor
Prepare the APQR report; Summarize the data collected in APQR preperation; Assist supervisor in preparing recommendations based on APQR evaluation
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