Overview
Join to apply for the Pharmaceutical Development Analyst role at TieTalent. This is an exciting opportunity to carry out high-quality analytical testing for complex pharmaceutical products in a GMP-regulated environment, with a focus on respiratory and inhalation drug products.
Key Responsibilities
* Perform experimental testing of pharmaceutical products using validated analytical methods.
* Prepare and handle solutions, mobile phases, and reagents in line with internal SOPs.
* Accurately record and analyse data in accordance with GMP and ALCOA+ principles.
* Use analytical equipment (e.g., HPLC) with appropriate training and calibration.
* Communicate results clearly with senior scientific staff and cross-functional teams.
* Maintain an up-to-date training record and follow health & safety protocols at all times.
* Ensure all work meets regulatory standards including GMP, ICH, and COSHH.
About You
Essential
* A degree in a scientific field such as Chemistry, Pharmaceutical Sciences, or a related discipline.
* Experience working in a laboratory setting.
* A strong sense of organisation and attention to detail.
* Excellent data recording and documentation skills.
Desirable
* Experience with HPLC or similar analytical instrumentation.
* Knowledge of GMP/GLP standards and pharmaceutical regulatory guidelines.
* Previous work in respiratory or inhalation product development.
Why Apply
* Work with an industry-leading organisation with cutting-edge facilities.
* Contribute to the development of life-changing respiratory therapies.
* Join a supportive team committed to your professional growth.
* Site-based role with up to 10% travel for training or project support.
How to Inquire
If you would like to join a market-leading CRO within the global pharmaceutical industry, please apply today or contact Gareth Gooley for more information.
Additional Details
Location: Newport, England, United Kingdom (and surrounding opportunity postings may appear).
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