LSC have a great contract opportunity for a Laboratory Project Engineer to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.
If you have 4+ years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect project for you!
If you have experience of working in GMP Quality Management Systems in a laboratory or manufacturing environment and the ability to keep work pace and meet deadlines, this role could be a good fit for you.
It is essential to have good organisation and planning skills, strong leadership, communication skills, critical thinking, and customer management skills.
If you have proven success working well in a team environment with flexibility to react to changing business needs, ability to anticipate, evaluate and resolve multiple, simultaneous operational issues, in addition to the ability to work independently with minimum direct supervision, we encourage you to apply!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Ensure that all work on Lab IT and Benchtop Analytical equipment is carried out in a compliant manner, meets 21 CFR Part 11, EU Annexe 11, cGLP/GMP's, and Corporate & local BMS compliance requirements.
- Support the introduction of new instrument systems.
- Work with all departments, QA, QC, CSV, NQC Engineering, and with contract vendors.
- Working with external laboratory suppliers to assist, configure and commission benchtop equipment.
- Take ownership of equipment in receiving deliveries and keeping track from delivery to commissioning.
- Technical design engineer for the Lab IT/GMP/Regulatory systems including integration to other systems such as Chromatography and Benchtop analytical equipment.
- Work under the direction of the IT Applications manager and with other team members from the corporate laboratory systems team to deliver systems and interfaces.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Degree in Engineering, Information Systems, Computer Science or Life Sciences.
- At least 4 years' experience of working in a pharmaceutical laboratory environment, with IT experience of laboratory instrument systems.
- Experience with Solovpe, FIT, Osm, Raman systems.
- Good working understanding of Windows file permissions, networking, Active Directory, Group Policies.
- Thorough knowledge of Pharmaceutical Industry Regulations (cGMP/cGLP, OSHA, EPA/EQB), 21 CFR 11 and EU Annex 11 as they relate to Lab IT systems.
Applicants interested in our contracting opportunities within the pharmaceutical sector in Ireland are required to have a Stamp 1G or a Stamp 4 visa. Please note that we are unable to provide visa sponsorship. Thank you for your understanding.
Apply via this advert or contact Paul O'Driscoll on 021 4777 329 if you have any more questions about this opportunity!
