Scientist 1 – Drug Product Process Development

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 companys success. Join us on our journey towards sustainable growth creating real impact on patients and society!

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Join Our Award-Winning Team at Ipsen Wrexham

At Ipsen we are committed to improving the lives of patients with a special focus on advancing neuroscience therapies. Our Wrexham site is a vital part of this mission delivering cutting-edge solutions in a dynamic and collaborative environment. We are proud to be Great Place to Work certified and a Shingo Bronze Medallion holder reflecting our commitment to excellence innovation and continuous improvement.

With a recent 24 million investment in the site and a further 86.4 million expansion underway there has never been a more exciting time to join us. If you are passionate about making an impact and want to be part of a team that values growth innovation and excellence then Ipsen could be where you thrive.

Role Summary
As a Scientist 1 Drug Product Process Development you will assist in the execution of Drug Product / Fill Finish development studies to define robust drug product manufacturing processes and develop understanding of drug product attributes. You will support Drug Product plans and strategies that enable clinical supply.

In this role you will:

• Assist in aspects of Drug Product Development to define manufacturing processes and understand Drug Product attributes both internally and via CDMOs
• Write and execute protocols required within Drug Product Development
• Work under general supervision to meet project goals
• Carry out laboratory work with a high rightfirsttime rate
• Ensure experimental work is recorded appropriately in controlled laboratory notebooks or protocols in line with GxP and ALCOA data integrity principles
• Perform analytical assays in support of development studies

Additional Responsibilities

• Perform technical review of data for aspects of drug product development studies and reports
• Prepare accurate and precise technical reports
• Lead aspects related to process or general improvements in a specific area
• Maintain and contribute to the successful running of laboratory areas in line with GxP
• Manage laboratory consumables and ensure equipment maintenance and calibration are performed in line with approved procedures
• Conduct routine sampling testing and cleaning to maintain laboratory equipment and facilities
• Operate equipment safely in accordance with cGXP GMP and Health & Safety requirements and ensure defective equipment is reported and repaired
• Act as a trainer to other Scientists
• Work effectively within GMP and EHS requirements at all times

Requirements
Essential:

• Degree in an appropriate scientific discipline or equivalent laboratory working experience
• Ability to work in a GMPregulated environment
• English language proficiency

Preferred:

• Relevant industry laboratory experience

Role Details
Location: Wrexham
Working Pattern: Fully onsite

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