Pharmaceutical Analyst
Job description
Original text imported from Reed
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.
Key skills
AI-extracted from the job advert
Application advice
5 AI-generated recommendations to maximise your chances.
⭐ Highlight your HPLC experience prominently as this is the key analytical technique mentioned for pharmaceutical testing
📊 Quantify your laboratory experience: 'Performed 150+ HPLC analyses monthly with 99.2% accuracy'
🌐 Emphasise GMP and ALCOA+ knowledge as these are critical regulatory requirements for this role
🎯 Showcase any respiratory or inhalation product experience as this is their specialist focus area
🤝 Demonstrate cross-functional collaboration skills as you'll work with senior scientific staff across teams
Suggested CV bullets
3 bullets our AI drafted for this specific advert, mirroring its ATS keywords.
Add these 3 bullets under your most recent experience:
- •Performed 200+ HPLC analyses monthly for pharmaceutical products, achieving 99.5% accuracy in GMP-regulated laboratory environment
- •Prepared mobile phases and reagents following validated SOPs, supporting 15 concurrent drug development projects
- •Applied ALCOA+ principles to document analytical data for 8 respiratory drug formulations, ensuring full regulatory compliance
Free to copy — tailoring requires a 30-sec CV upload.
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Letter preview — tailored to Smart4Sciences
Dear Hiring Manager,
Smart4Sciences' focus on respiratory and inhalation drug products aligns perfectly with my analytical chemistry background and passion for pharmaceutical development. My experience with HPLC instrumentation and GMP compliance makes me well-suited for this Pharmaceutical Development Analyst position.
My background in analytical testing and laboratory work has equipped me with the technical skills and attention to detail required for this role. I am particularly drawn to the opportunity to work with validated analytical methods and contribute to product development projects in a regulated environment.
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Interview questions
10 questions generated from this advert.
Technical
- ›Explain the ALCOA+ principles and how you apply them in data recording
- ›Walk me through your HPLC method validation experience
- ›How do you ensure GMP compliance when preparing mobile phases?
- ›What are the key differences between GMP and GLP standards?
- ›Describe your experience with respiratory drug product analysis
Behavioural
- ›Tell me about a time when your attention to detail prevented a significant error
- ›Describe a situation where you had to communicate complex analytical results to non-technical stakeholders
- ›Give an example of when you had to work under pressure to meet regulatory deadlines
- ›Tell me about a time you identified and resolved a problem with analytical equipment
- ›Describe how you prioritise multiple analytical testing projects simultaneously
STAR answer examples
Model answers using the Situation-Task-Action-Result framework. Adapt to your own experience.
Tell me about a time when your attention to detail prevented a significant error
Describe a situation where you had to communicate complex analytical results to non-technical stakeholders