Title:
Senior QC Laboratory Analyst
Company:
Ipsen Biopharm 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:
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!
Are you passionate about ensuring the highest quality standards in pharmaceutical products? Join our dynamic QC Operations team as Senior QC Laboratory Analyst! In this role, you will perform critical analytical testing to support batch release, stability monitoring, and more. You'll be at the forefront of maintaining compliance with GLP, GMP, and regulatory requirements, while also contributing to exciting project work and laboratory coordination.
Key responsibilities:
- Perform Analytical Testing: Conduct testing of drug products and APIs for batch release and stability assessment and analyse various samples including customer complaints and raw materials.
- Maintain Laboratory Equipment: Ensure all laboratory equipment is maintained according to company policies and perform regular stock checks on samples and reagents.
- Coordinate and Train: Assist in the day-to-day running of the laboratory, initiate and perform training of test methods, and support equipment projects.
- Ensure Compliance: Adhere to GMP requirements, report compliance concerns, and ensure all training is up to date and documented.
- Drive Continuous Improvement: Review lab methods for compliance, perform internal inspections, and lead process improvement initiatives.
- Support Projects: Represent QC on project teams, support and lead QC-related projects, and participate in audits and inspections as a subject matter expert.
Knowledge, skills & experience:
- Degree in a relevant science based subject or equivalent experience
- Experience performing lab investigations in a GMP setting
- Continuous improvement mindset, methodical, attentive to detail
If you thrive in a fast-paced environment and are eager to make a meaningful impact, this is the perfect opportunity for you!
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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.