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NPI Quality Control Senior Associate
- Dublin, Dublin, Ireland
- Dublin, Dublin, Ireland
À propos
Find out exactly what skills, experience, and qualifications you will need to succeed in this role before applying below.
If you have 2-3 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, if this sounds like your next move, we'd love to hear from you.
Contract | Dublin | Duration: 12 months ABOUT THE PROJECT
- KEY RESPONSIBILITIES:
* QC Representative for NPI activities and routine Product meetings.
* Manage all sample management activities related to NPI activities throughout the site.
* Create/own and approve protocols, sample plans, SOP and documentation related to NPI.
* QC Representative responsible for Method Validation and Transfers co-ordination and readiness.
* Sample shipments and temperature monitoring activities for NPI activities.
* LIMS data coordination of non-core (NPI) activities.
ABOUT YOU
- ARE YOUR SKILLS A MATCH?
* Bachelor's degree in a science discipline.
* 2-3 years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
* Strong background in Chemistry and Analytical testing is required.
* Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.
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 Jenny Murphy on if you have any questions about this role.
Find out more about working with LSC at To From Record Yes No Always use these settings Skills: quality control NPI activities safety compliance
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Compétences linguistiques
- English
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