LSC have a great contract opportunity for a Sr Document Controller to join the client project team on a major Dublin based Biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that can help patients overcome serious diseases and improve their quality of life.
The role is fully embedded on site and responsible for the client-side control and governance of all project documentation across design, construction, CQV and handover phases.
If you are an experienced Document Controller with 5 + years experience in a similar role this could be the next contract for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
· Client-side control of all project documentation across the full lifecycle
· Manage document receipt, review, approval, issue, revision control and archiving
· Interface with EPCM partners, vendors, contractors and internal stakeholders
· Ensure documentation complies with GMP, data integrity and ALCOA+ principles
· Maintain accurate document registers, trackers and status reports
· Support CQV documentation, executed protocols and final turnover to operations
· Support audits, inspections and project close-out activities
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
· Proven experience as a Document Controller on pharmaceutical or life sciences capital projects
· Essential: hands-on experience using EIDA for document management
· Experience working client-side or within an owner's project team
· Strong understanding of GMP documentation requirements
· Experience supporting construction, commissioning and qualification documentation
· Ability to work full-time on a live pharmaceutical site in Ireland
Desirable
· Experience on large-scale Irish pharma projects (drug product, biologics, sterile facilities)
· Familiarity with ValGenesis, Kneat, ACC or similar platforms
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 Siobhan Cummins on 021 4777329 if you have any questions about this role.
Find out more about working with LSC at lscconnect.com
