MDI Analytical Chemist
orbia
| Company | orbia |
| Category | Uncategorised |
| Location | — |
| Remote | — |
| Employment | Not stated |
| Level | Not stated |
| Salary | Not stated by the employer |
| Posted | 14 Jul 2026 |
| Last verified | 3 Aug 2026 |
| Source | Employer career page (teamtailor) |
Description
About Orbia Fluor & Energy Materials: What if your work could shape the materials that power everyday life — from the cities we live in, to the healthcare we rely on, to the technologies driving our future? At Orbia Fluor & Energy Materials (OF & EM), this is exactly what we do. Count on a welcoming environment where purpose meets impact. Here, we collaborate across the Americas, Europe and Asia to develop, manufacture and supply fluoroproducts that play a fundamental role in advancing life around the world. We foster a culture where diverse perspectives are valued, where you can contribute authentically, and where innovation and well-being go hand in hand. We encourage our people to grow, explore new solutions and become the best version of themselves. You will join an international, professional team and benefit from a competitive compensation package. Orbia Fluor and Energy Materials, an Orbia business, is looking for an MDI Analytical Chemist to be based at Thornton Science Park, Cheshire, UK. Main Purpose Support the MDI Services business analytical testing requirements in compliance with applicable cGMP guidelines and internal procedures. Main Responsibilities · Source, install and qualification of Analytical Equipment. · Development, Validation, verification and transfer of Analytical Test Procedures (including pharmacopeial verification) to and from the Orbia F&EM MDI services facility. · Sampling and incoming inspection of raw materials and components in line with approved procedures or monographs. · Testing to support development studies and clinical batch release of Metered Dose Inhalers (MDI’s) including in-process, finished product and stability MDI samples, Cleaning Verification and environmental monitoring sampling. · Lead and participate in Analytical Investigations, manufacturing deviations and remediation as required. · Drive ownership and completion of Deviation, CAPA, Change Controls, Analytical Investigations and other PQS records to agreed timings. · Management & co-ordination of planned preventative maintenance for Laboratory Equipment · Support MDI continual Improvement activities as required. · Creation and updates of SOP's, Analytical Test Methods, and specifications to support QC testing activities as required. · Conduct EHS COSHH/risk assessment and recommend improvements to laboratory procedures, techniques and technologies. · Maintain inventory control of materials, equipment and consumables, and re-order stocks as required. · Develop training material and provide training to other members of Orbia F&EM MDI Services team. · Supervise temporary staff and students working in the laboratory. Qualifications · Bachelor’s Scientific Degree (Chemistry, Physics, Biology or equivalent) Knowledge/ Experience Required · 5 years+ experience in an accredited (ideally GMP) analytical laboratory working with HPLC/GC. · Ability to work independently and proactively within a regulated pharmaceutical environment. · Excellent interpersonal skills and ability to communicate effectively with internal/external customers, stakeholders and regulators/auditors. · Critical thinking and excellent problem solving & root cause analysis skills. · A strong background in HPLC and or GC analysis and troubleshooting is essential. · Experience and knowledge of key analytical techniques such Moisture analysis, FT-IR spectroscopy. · Equipment qualification and calibration. · Method development and validation including cleaning verification. · Ideally, experience in handling and testing pressurized gases or Metered Dose Inhalers (including NGI/ACI, Delivered Dose Uniformity techniques but this is not essential). · Ideally, experience of testing in line with recognized Pharmacopeia but not essential. · Ability to work to approved quality and safety procedures and recognize and propose opp
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