Pharmaceutical Development Analyst

TieTalent; Newport; On-site; GBP 30,000 - 40,000; Full time

Benefits offered by this job

Supportive team environment

Professional growth opportunities

Work with cutting-edge facilities

Job summary

A market-leading CRO in Newport, England, is seeking a Pharmaceutical Development Analyst. This role involves high-quality analytical testing for complex pharmaceutical products in a GMP-regulated environment. The ideal candidate will hold a degree in a scientific field and have experience in laboratory settings. Join a supportive team committed to developing life-changing respiratory therapies.

Qualifications

• A degree in a scientific field such as Chemistry or Pharmaceutical Sciences.
• Experience working in a laboratory setting.
• Excellent data recording and documentation skills.

Responsibilities

• Perform experimental testing of pharmaceutical products using validated methods.
• Prepare and handle solutions, mobile phases, and reagents.
• Accurately record and analyse data in accordance with GMP standards.

Skills

Attention to detail

Data recording

Organisational skills

Education

Degree in a scientific field

Tools

HPLC

Job description

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).