Title:
QC TechnologistCompany:
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:
An excellent opportunity has arisen for a QC Technologist to join our Quality Control team on a fixed-term contract, covering maternity leave until 29 January 2027. You’ll build experience across a broad range of analytical techniques, with a strong focus on high-quality results and robust documentation in a GLP environment. Hours: 10am–6:30pm Mon–Thurs, 10am–5pm Fri.
In this role, you’ll analyse API and raw material samples to approved methods, delivering results on time and to the right quality standards. It’s a great opportunity to deepen your hands-on lab skills with structured training, coaching from experienced colleagues, and exposure to regulated ways of working (GLP/GMP).
What you’ll do
Analyse API batches to approved analytical SOPs and specifications using techniques such as HPLC, UV, pH, Karl Fischer and Mass Spec.
Support the daily test schedule, including mobile phase preparation and sample weighing.
Complete required training (including external and site-based training where needed) and build capability across all techniques performed; support other Technologists and help train new starters as appropriate.
Compile results and submit for review in a timely manner, with close attention to SOP requirements, documentation standards and data integrity.
Raise quality events and OOS/OOT results promptly in discussion with senior colleagues, and support timely investigations including RCA and CAPA; escalate issues that could impact testing and release schedules.
Maintain strong laboratory standards: promote accuracy and precision in daily routines; complete equipment calibration activities; support inspection readiness; follow Ipsen safety and environmental policies; and contribute to OE initiatives (e.g., 5S) and good housekeeping.
Support the wider QC operation: purchase/manage consumables and reagents; generate SOPs/test methods/risk assessments as required; liaise with other Ipsen sites for information transfer and troubleshooting; and coordinate sample and reference standard shipments.
To succeed, you’ll have a science degree (or equivalent) and hands-on laboratory experience in a GLP environment, with exposure to controlled methods, clear documentation, and data integrity expectations. Experience with chemistry test methods (including chromatography) is important, and any GMP experience is a plus.
Why Ipsen
At Ipsen, you’ll be part of a team driven by patient impact—working collaboratively, acting with integrity, and continuously improving how we deliver quality medicines. You’ll join an environment where your expertise is valued, your development is supported, and your work makes a meaningful difference.
If this sounds like the right next step for you, we’d love to hear from you—apply today and help us deliver what matters most.
#LI-ONSITE
We are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace “The Real Us”. The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve. This means we also want to help you perform at your best when applying for a role with us. If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application.Ipsen Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Ipsen and has not been reviewed or approved by Ipsen.
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Healthcare Strength — Health coverage is described as comprehensive, with broad medical, dental, and vision offerings. Company materials emphasize a wide-ranging package that supports overall wellbeing.
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Retirement Support — Retirement programs are highlighted with a competitive 401(k) match and access to an employee stock purchase plan. These elements are frequently cited as strengths in the package.
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Parental & Family Support — Family support includes paid parental leave and company-provided backup child and elder care. These programs complement core benefits and add practical day-to-day value.
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What We Do
Ipsen is a French leading global mid-size biopharmaceutical company headquartered in Paris, France focusing its efforts where unmet medical needs are greatest. Ipsen develops and commercializes innovative medicines in three key therapeutic areas - Oncology, Rare Disease and Neuroscience. We have over 5000 employees worldwide and our medicines are registered in more than 100 countries, with direct commercial presence in over 30 countries. Ipsen has 4 global R&D hubs and 3 pharmaceutical development centers around the world







