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Pharmaceutical Development Analyst

Smart4Sciences
Posted a month ago, valid for a month
Location

Newport, Newport NP20 7AE, Wales

Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

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Sonic Summary

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  • Smart4 Sciences is seeking a Pharmaceutical Development Analyst for an established pharmaceutical services provider.
  • The role involves conducting high-quality analytical testing for complex pharmaceutical products in a GMP-regulated environment.
  • Candidates should have a degree in a scientific field and experience working in a laboratory setting, ideally with HPLC or similar instrumentation.
  • The position offers a salary of £30,000 to £35,000 per year and requires at least 1-2 years of relevant experience.
  • This is a site-based role with up to 10% travel for training or project support, within a motivated and supportive team.

Are you a detail-driven scientist with a passion for analytical testing and pharmaceutical development?

Smart4 Sciences are working with an established and innovative pharmaceutical services provider to recruit a Pharmaceutical Development Analyst into their Pharmaceutical Development team.

The Role

This is an exciting opportunity to carry out high-quality analytical testing for complex pharmaceutical products in a GMP-regulated environment. You'll be an integral part of a specialist team working on product development projects 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.

You'll be joining a motivated team and a business that values integrity, innovation, and continuous improvement.

?? 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).

If you would like to join a market leading CRO within the global Pharmaceutical industry please apply today or contact Gareth Gooley on for more info

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

SonicJobs' Terms & Conditions and Privacy Policy also apply.