Are you ready to be at the forefront of biotechnology excellence?
LSC have a fantastic contract opportunity for an QA Associate to join a Cork-based biopharmaceutical company. The site manufactures low-volume bulk API for clinical and commercial supply, covering mammalian cell culture growth, purification, formulation, and filling. The company is committed to advancing breakthrough treatments through cutting-edge science and cross-functional collaboration.
If you have 4 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 | Cork | Duration: [12 months]
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Provide Quality direction and oversight of the start-up, technical transfer, operation, and continuous improvement of Sterile Drug Product Filling operations.
- Provide Quality input to Change Controls, Protocols and Reports ensuring scope of records are clear and implementation activities are robust and timely.
- Write, review and approve Standard Operating Procedures, Work Instructions, Quality Technical Agreements, Master Batch Records, Specifications and other GMP documentation
- Participates within inter-departmental and cross-functional project teams to immediately address issues and questions in real time to help ensure project timelines are achieved.
- Prioritizes tasks to ensure the critical tasks are completed on time and meet requirements.
- Provide Quality input and guidance to ensure Lot Release (Components/Raw Materials/Drug
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Degree or 3rd level qualification (Science, Quality). QP Qualification would be an advantage.
- Demonstrated experience in Sterile Drug Product Filling and start-up of same.
- Relevant experience (5yrs +) working in a Quality function in the pharmaceutical or biotechnology industry or other combination of experience and educational background that may otherwise satisfy the other requirements of the role.
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 4781212 if you have any questions about this role.
Find out more about working with LSC at lscconnect.com
