QC Microbiology Specialist

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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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!

As a QC Microbiology Specialist youll support technical operations through microbiological testing data review investigations and continuous improvement initiatives. Youll be part of a collaborative team that values precision innovation and safety - working on exciting new development projects and contributing to a culture of excellence. This is a shift based position consisting of 4 on/4 off days 8am-7pm.

Key Responsibilities:

• Perform and review microbiological testing of raw materials in-process samples and final products.
• Lead investigations into OOS/OOT results and support CAPA implementation
• Conduct environmental and utility monitoring in cleanroom and controlled environments
• Maintain and calibrate laboratory equipment and ensure inspection-readiness
• Provide training in microbiological techniques and support team development
• Drive process improvements and support validation and project work

Knowledge skills & experience:

• Experience in a similar role in a GMP-regulated microbiology lab (pharma or biopharma)
• Proficiency in environmental monitoring bioburden testing and microbial identification
• Degree in a relevant life sciences subject (Microbiology preferred)
• Ability to work according to shift pattern (4 on/4 off days 8am-7pm)

If youre detail-oriented proactive and thrive in a fast-paced lab environment wed love to hear from you. Apply now to be part of a team thats shaping the future of pharmaceutical quality.

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