Are you ready to be at the forefront of biotechnology excellence?
LSC have an exciting contract opportunity for a senior scientist to join a leading biopharmaceutical company in Dublin. This is an exciting opportunity to join a high-performing team in a cutting-edge manufacturing environment, where you will play a key role in supporting critical quality control operations and driving continuous improvement.
If you have 10 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:
- Support the Senior Manager in identification, documenting, and driving commercial stability user requirements for a future state LIMS system.
- Serve as a point of contact for the stability user group in order to liase with business and process owners and direct management, with the intent on developing, managing, and executing stability strategies related to the future and current state LIMS system.
- Serve as a technical expert within the Sample Manager LIMS and Labware systems in order to support mapping multiple current state LIMS processes to a singular future state, centralized LIMS system.
- Support static builds, migrations, and system updates to enhance current stability operations for critical ongoing Run-the-Business requirements.
- Support and or manage user ticket requests to ensure available stability support and completion.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Bachelor of Science (BS), at a minimum, with at least 10 years of experience within the pharmaceutical industry: at least 5 years of stability product/program experience and 5 years developing and executing LIMS strategies to support the stability program.
- Must be able to understand stability process, quality, and integrated validated systems, in context of multiple LIMS systems.
- Experience in processing LIMS tickets, demands, and enhancements requiring successful UATs.
- Strong understanding of GMP requirements
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.
Apply via this advert or contact Kathy Gillen on 021 4777329 if you have any questions about this role.
Find out more about working with LSC at lscconnect.com
