LSC have a great contract opportunity for an Upstream Bioprocess Associate to join a 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.
If you have 3+ years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Execute commercial upstream biopharmaceutical manufacturing processes in accordance with GMP requirements, SOPs and established work instructions.
- Operate and monitor large-scale manufacturing equipment, ensuring safe and efficient production operations within a 24/7 shift environment.
- Create, review and update manufacturing documentation, including SOPs, batch records and operating procedures.
- Utilise process automation and manufacturing systems, including DeltaV, Syncade MES, OSI/PI Historian and SAP.
- Support manufacturing investigations, deviation management, process optimisation and continuous improvement initiatives.
- Collaborate with Manufacturing, Engineering, CQV, Automation and Quality teams to support equipment commissioning, qualification, validation and operational readiness.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Minimum Level 6 qualification in Science, Engineering or a related discipline, or relevant experience in a regulated manufacturing environment.
- 3+ years' experience in large-scale biopharmaceutical manufacturing, ideally within upstream processing, with strong GMP knowledge.
- Experience with DeltaV, MES or similar process control systems, excellent problem-solving and communication skills, and flexibility to work a 24/7 shift pattern.
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!
Apply via this advert or contact Andrea McSweeney on 021 4777329 if you have any more questions about this role!
