QC Senior Analyst
The Quality Team at CPL are seeking a Quality Control Senior Analyst to join the QC Department, reporting directly to the QC Team Lead.
This role involves testing, reviewing and releasing raw materials, intermediates and active pharmaceutical ingredients in the Quality Control Laboratory.
The successful candidate will:
* Provide technical support for instrumentation and analytical methodology, executing troubleshooting as required.
* Offer coaching and training on instrumentation and analytical methodology within the QC laboratory.
* Plan and approve materials to meet shipping and production timelines, stability timelines and quality control metrics.
* Coordinate and lead laboratory/site investigations.
* Identify and investigate out-of-trend/adverse results present in analytical results.
This position requires excellent interpersonal and communication skills, working as part of a Lean Lab team-based structure.
You will be using classical analytical technologies including Raman, FTIR, KF, alongside modern analytical techniques such as HPLC, GC, ICP-AES, ICP-MS and wet chemistry techniques.
A key aspect of this role is participating in daily huddle meetings and short interval control boards.
To be considered for this role, you will require:
* A BSc in Analytical Science, Chemistry or a related discipline.
* Minimum of 3 years' experience in analytical chemistry.
* Highly motivated individual with strong teamwork skills, proven success of working in team environments and flexibility to react to changing business needs.
Demonstrated experience in Operational Excellence, 5s, Lean Labs, yellow belt certification and yellow belt projects is desirable.
In addition to a competitive base salary, the successful candidate can expect:
* Excellent opportunities for career enhancement and personal development.
* Annual bonus linked to business results.
* A well-established further education program.
* Pension scheme.
* Private Healthcare Insurance.