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Ipsen

QA Technologist

Reposted 25 Days Ago
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Dublin
Mid level
Dublin
Mid level
The QA Technologist at Ipsen will ensure compliance with cGMP regulations and guidelines, support quality processes, review batch records, compile cGMP documentation, conduct training, and be part of the QA team for production documentation.
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Title:

QA Technologist

Company:

Ipsen Manufacturing Ireland Ltd


 

About Ipsen:

Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation.

 Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society!

For more information, visit us at https://www.ipsen.com/ and follow our latest news on LinkedIn and Instagram.

Job Description:

Ipsen in Ireland is represented by a dynamic state-of-the-art manufacturing facility, creating API for our key products.

We now have an opportunity for a QA Technologist to join our Quality team in Dublin.  This opening is available on a 1 year fixed term contract.

About the role

As QA Technologist, you will assist in ensuring that company operations and operating procedures are in compliance with all appropriate cGMP regulations and guidelines. Contribute to Quality processes/ initiatives at a local level as required. 

What will you be doing…

  • Review of Batch Record Documentation

  • Compilation, Review and Approval of cGMP Documentation

  • Conduct on-site cGMP training

  • Work as part of the QA Team to support the production plan-documentation and batch record review

What are we looking for…

  • BSc in Science

  • Relevant experience working with QA

  • Knowledge of cGMP as it relates to API

  • In- Depth knowledge of Quality Systems and their maintenance/implementation in API sites

  • Team-workng and excellent communication skills

If this sounds like an exciting opportunity to apply your pharmaceutical industry experience in our Quality department, apply today!

#LI-ONSITE 

IPSEN is committed to equality of opportunity for all staff and applications, individuals are encouraged to apply regardless of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.

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