Job Description Summary
To perform IPQA activities at shop floor in each and every stage of sterile manufacturing and packing.Job Description
1. To perform IPQA activities at shop floor in each and every stage of sterile manufacturing and packing.
2. To perform sampling in each stage or whenever required during product manufacturing, filling and packaging activity.
3.Inprocess checks of Manufacturing, Filling and Packaging.
3. To Perform the AQL after completion of visual inspection of products.
4.To perform audit trail & electronic data review batch wise and as per schedule.
5.To handle the control sample and stability sample management.
6. To Involve in Qualification of master kit approval for Visual Inspection Activities.
7.To Review and approve all the documents relevant to visual inspector qualification.
Similar Jobs
What We Do
At Endo, our far-reaching vision is simple: to help everyone we serve live their best life. As a specialty pharmaceutical company, we’re motivated by a strong sense of purpose to find better ways to meet unique medical needs.
Our global team of passionate employees understands the importance of their work. We’re dedicated to supporting one another as we connect with communities and foster partnerships that elevate quality-of-life and bring the best treatments forward.
Our uncompromising commitment results in the delivery of life-enhancing therapies. From intelligent product selection to commercialization, we strive to make a meaningful, tangible impact to help everyone live their best life.
Endo has global headquarters in Malvern, Pennsylvania.
Community Guidelines:
1. Be respectful. Everyone who visits our page should feel comfortable and respected.
2. If we see a comment that violates anything in the following list, it may be removed.
• Comments that use profanity; personally attack or bully another individual; or are off-topic, misleading, factually inaccurate, political, spam, defamatory, discriminatory or promotional.
• Comments that are excessively repetitive and/or disruptive to the community.
• Comments that promote illegal activity, use copyrights or trademarks or are related to an ongoing legal matter.
• Comments that appear to be medical advice.
We reserve the right to remove a reply for any reason at any time.
3. Adverse Event Reporting: If we see a post about an adverse event, an Endo representative will need to contact you to find out more information to comply with regulatory guidelines. If you experience a side effect while using an Endo product, please consult your physician or pharmacist immediately. You may also report to the FDA at fda.gov/medwatch or 800-FDA-1088.
Replies from other users do not necessarily reflect the views of Endo. We do not endorse content added by other users.
