Cpl in partnership with SK biotek Ireland are seeking to recruit a Quality Control Chemist to join the QC Department.
This position is in the In-Process Control group in QC and involves shift work with shift allowance on top of a salary.
SK biotek Ireland, an SK pharmteco company, is a global Contract Development and Manufacturing organisation (CDMO) with state-of-the-art facilities in Korea, US, France, and Ireland. Our mission is to ‘make what matters for a healthy, happier world’, from grams to tonnes. The Swords Campus has led the way in the development, scale-up, and commercial manufacture of Active Pharmaceutical Ingredients (APIs) for almost 60 years. With a talented workforce and exceptional technical capabilities, we continue to produce some of the world’s most important medicines.
Position Description:
Reporting to the QC IPC Team Lead, the successful candidate will provide in-process analytical support to the manufacturing operations. The QC-IPC Chemist may also be involved in the testing of tankers, raw materials, intermediates, and active pharmaceutical ingredients in the Quality Control Laboratory. Working as part of a Lean Lab team-based structure, the QC-IPC Chemist will require excellent interpersonal and communication skills. The role will involve the use of classical analytical technologies including Raman, FTIR, KF, IR_LOD, in addition to modern analytical techniques including HPLC, GC, and wet chemistry techniques. Previous experience using Empower and Sample Manager is desirable. The QC-IPC Chemist will also be required to engage and fully participate in huddle meetings and short interval control boards.
Minimum Requirements:
1. A BSc in Analytical Science, Chemistry, or a related discipline is required.
2. A minimum of 3 years’ experience in analytical chemistry is required.
3. The desired candidate should be highly motivated, have strong teamwork skills, and proven success in a team environment with flexibility to react to changing business needs.
4. Experience in Operational Excellence, 5s, Lean Labs, and yellow belt projects is desirable.
5. The successful candidate will have a strong ability to manage their own workload and will contribute to various sub-teams in QC such as Safety, Equipment, or Audit Readiness. Experience in Investigation and Technical writing would be desirable.
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