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QA Digital Manufacturing Lead
- Limerick, Wexford, Ireland
- Limerick, Wexford, Ireland
À propos
Apply now, read the job details by scrolling down Double check you have the necessary skills before sending an application.
This company is transforming lives through groundbreaking medicines that treat serious diseases-from atopic dermatitis to high cholesterol and age-related blindness.
If you have 5 years of experience working in the pharmaceutical or biotechnology industry and are ready to take the next step in your career, if this sounds like your next move, we'd love to hear from you.
Contract | Limerick | Duration: 12 months ABOUT THE PROJECT
- KEY RESPONSIBILITIES: Provide QA leadership and guidance for the design and implementation of eBR and paperless manufacturing processes.
Define and approve review by exception (RBE) strategies, including deviation thresholds, exception handling, and QA review models.
Ensure digital manufacturing solutions are aligned with GMP, data integrity principles (ALCOA+), and applicable regulatory requirements (e.g., FDA, EU).
Partner with Manufacturing, Automation, IT, and Quality teams to embed quality-by-design into digital workflows.
Review and approve quality requirements, risk assessments, and validation/CSA deliverables related to digital plant systems.
ABOUT YOU
- ARE YOUR SKILLS A MATCH? Strong QA background in pharmaceutical manufacturing under GMP.
Hands-on experience with eBR, DeltaV, MES, or digital manufacturing systems.
Solid understanding of review by exception concepts and paperless batch release.
WHY LSC? LSC work exclusively in the Life Sciences sector.
Founded and run by contractors, we understand contracting first-hand and have created a unique approach to make the process as smooth as possible, so you can focus on delivering your best work.
With over 23 years' experience supporting the industry, we bring deep sector knowledge and long-standing client relationships.
At LSC, we partner with you for the long term, not just the duration of your contract.
We are committed to building lasting relationships and will work closely with you to ensure you are placed on projects that challenge, develop, and reward you throughout your career.
What You Can Expect.
Work on-site with leading biopharma organisations on high-impact projects Structured onboarding to ensure you're set up from day one Ongoing support and regular engagement from LSC throughout your assignment Be part of a wider LSC consultant network A dedicated team behind you; you're not navigating projects or contracts alone Note: Are you currently eligible to work in Ireland? As this is a contract opportunity, you will need to hold a Stamp 1G or Stamp 4 visa to apply. xyswxtq
Apply via this advert or contact Cian Marnane on if you have any questions about this role.
Find out more about working with LSC at Skills: quality assurance digital manufacturing pharmaceutical manufacturing
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Compétences linguistiques
- English
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