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- Tasks: Develop and validate analytical methods for pharmaceutical products.
- Company: Join a leading company in global pharmaceutical development and research.
- Benefits: Enjoy opportunities for mentorship, continuous improvement, and a dynamic lab environment.
- Why this job: Be part of cutting-edge research that impacts global health and innovation.
- Qualifications: Degree in Chemistry and 5 years' lab experience required.
- Other info: Located in beautiful Ireland, with a focus on compliance and quality.
The predicted salary is between 36000 - 60000 £ per year.
We are working with a company that sources top-level Scientists to join cutting edge research labs throughout the world. They are looking to hire a Senior Analyst to support a client who is a global leader in Pharmaceutical development and manufacture. As a Senior Analyst you will be responsible for the development & optimisation of analytical methods along with the validation and transfer of methods in line with regulatory standards.
What you’ll be doing:
- Develop, validate, and transfer analytical methods as per regulatory standards.
- Support new product introductions and technical troubleshooting.
- Ensure compliance with GMP and ALCOA+ principles in all documentation and lab work.
- Review and approve SOPs, protocols, and risk assessments.
- Train and mentor analysts, supporting continuous improvement initiatives.
- Communicate effectively with clients, delivering timely project updates.
Who we’re looking for:
- Minimum of a degree in Chemistry (or related subject).
- 5 years’ experience in a Pharmaceutical/analytical laboratory setting.
- Experience utilising instruments such as HPLC, GC, LC-MS etc to analyse API’s, raw materials & excipients.
- Method development & validation experience.
- Working knowledge of GMP regulations.
If you or someone in your network is looking for a lab-based position focusing on pharmaceutical method development, please get in touch!
Method Development & Validation Specialist employer: VRS-UK
Contact Detail:
VRS-UK Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Method Development & Validation Specialist
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who have experience in method development and validation. Attend relevant conferences or webinars to connect with potential colleagues and learn about the latest trends in analytical chemistry.
✨Tip Number 2
Familiarise yourself with the specific instruments mentioned in the job description, such as HPLC, GC, and LC-MS. If you can, gain hands-on experience or take online courses to enhance your skills and demonstrate your proficiency during interviews.
✨Tip Number 3
Prepare to discuss your previous experiences in method development and validation in detail. Be ready to provide examples of how you've ensured compliance with GMP regulations and how you've contributed to continuous improvement initiatives in your past roles.
✨Tip Number 4
Research the company and its clients thoroughly. Understanding their products, values, and recent developments will help you tailor your conversations and show your genuine interest in the role during interviews.
We think you need these skills to ace Method Development & Validation Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in method development and validation. Include specific examples of analytical methods you've developed or optimised, and any instruments you have used, such as HPLC or LC-MS.
Craft a Compelling Cover Letter: Write a cover letter that directly addresses the job description. Emphasise your experience in pharmaceutical laboratories and your understanding of GMP regulations. Show enthusiasm for the role and how your skills align with the company's needs.
Highlight Relevant Skills: In your application, clearly outline your technical skills related to method development and validation. Mention your experience with compliance documentation and training others, as these are key aspects of the role.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in a laboratory setting.
How to prepare for a job interview at VRS-UK
✨Showcase Your Technical Expertise
Be prepared to discuss your experience with analytical methods and instruments like HPLC, GC, and LC-MS. Highlight specific projects where you developed or validated methods, as this will demonstrate your hands-on knowledge and suitability for the role.
✨Understand Regulatory Standards
Familiarise yourself with GMP and ALCOA+ principles, as compliance is crucial in this field. Be ready to explain how you've ensured adherence to these standards in your previous roles, which will show your commitment to quality and regulatory requirements.
✨Prepare for Problem-Solving Questions
Expect questions that assess your troubleshooting skills. Think of examples where you faced challenges during method development or validation and how you resolved them. This will highlight your analytical thinking and ability to work under pressure.
✨Emphasise Communication Skills
Since the role involves communicating with clients and mentoring analysts, be prepared to discuss your communication style. Share examples of how you've effectively delivered project updates or trained team members, showcasing your ability to collaborate and lead.
