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For Companies At a Glance
- Tasks: Support chemistry projects through analytical lab work and lead a team of analysts.
- Company: Join a well-established CRDMO working with global biotech and pharmaceutical companies.
- Benefits: Enjoy a permanent role with opportunities for career growth and development.
- Why this job: Be part of innovative projects that impact the biotech industry while working in a collaborative environment.
- Qualifications: Degree in Chemistry or related field with hands-on expertise in HPLC/GC and GMP standards.
- Other info: Located in Macclesfield, this role offers a chance to lead and innovate in analytical development.
The predicted salary is between 36000 - 60000 £ per year.
CK Group are recruiting for an experienced Analytical Development Scientist, to join a Contract Research & Development and Manufacturing Organisation (CRDMO), working with innovator biotech and pharmaceutical companies globally, who are based in Macclesfield, on a permanent basis.
Company: This company is well established and growing with R&D facilities globally.
Location: The role is based on site in Macclesfield, Cheshire.
Role:
- Support chemistry projects, through analytical lab-based work, develop, validate and carry out technical transfer of analytical methods and release analysis (GMP and non-GMP).
- Developing, troubleshooting and validating analytical methods.
- Planning and executing analytical work to meet project timelines with minimal supervision.
- Working within multi-functional project teams operating to tight deadlines.
- Able to work effectively to GMP quality standards.
- Opportunity to lead the analytical aspects of projects and lead a team of analysts to plan, supervise and execute analytical work to meet project timelines.
Your Background:
- Educated to degree level or above in Chemistry, Analytical Chemistry or a related field.
- A background in Analytical Chemistry combined with demonstrated in-depth, hands-on expertise in HPLC/GC and experience of other analytical methodologies utilised to characterise APIs, intermediates and raw materials.
- Experience in other analytical methodologies such as techniques for identity or form determination (e.g. NMR, MS, IR, XRD).
- Understanding of GMP quality standards.
- Demonstrated analytical expertise supporting early, mid or late-phase route and process development of APIs, intermediates and raw materials.
- Experience in contracting analytical testing with third parties and leading communications with customers.
- Experience in regulatory requirements for the development and validation of LC/GC methods for content and the separation of impurities and degradation products in APIs including trace level analysis.
- Experience in out of specification and atypical result investigations.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 120 653 in all correspondence.
Contact Detail:
New Scientist Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Analytical Development Scientist
✨Tip Number 1
Familiarise yourself with the specific analytical techniques mentioned in the job description, such as HPLC and GC. Being able to discuss your hands-on experience with these methods during an interview will demonstrate your suitability for the role.
✨Tip Number 2
Research the company’s recent projects and developments in the biotech and pharmaceutical sectors. This knowledge will not only help you tailor your conversation but also show your genuine interest in their work and how you can contribute.
✨Tip Number 3
Prepare to discuss your experience with GMP quality standards and how you've applied them in previous roles. Highlighting specific examples of how you've ensured compliance can set you apart from other candidates.
✨Tip Number 4
Network with professionals in the industry, especially those who have worked in similar roles or companies. Engaging with them on platforms like LinkedIn can provide valuable insights and potentially lead to referrals for the position.
We think you need these skills to ace Analytical Development Scientist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your educational background in Chemistry or Analytical Chemistry, as well as your hands-on experience with HPLC/GC and other analytical methodologies. Use specific examples to demonstrate your expertise.
Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Mention your experience with GMP quality standards and your ability to work within multi-functional teams. Be sure to reference the job title and job reference number (120 653) in your application.
Showcase Relevant Experience: Detail your previous roles where you developed, validated, and executed analytical methods. Highlight any leadership experience you have in managing teams or projects, especially in a GMP environment.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for an Analytical Development Scientist.
How to prepare for a job interview at New Scientist
✨Showcase Your Technical Expertise
Be prepared to discuss your hands-on experience with analytical techniques like HPLC and GC. Highlight specific projects where you developed or validated methods, as this will demonstrate your capability to handle the technical demands of the role.
✨Understand GMP Standards
Familiarise yourself with Good Manufacturing Practice (GMP) quality standards. Be ready to explain how you've applied these standards in previous roles, as this is crucial for the position.
✨Demonstrate Team Leadership Skills
Since the role involves leading a team of analysts, prepare examples of how you've successfully led projects or teams in the past. Emphasise your ability to plan, supervise, and execute analytical work under tight deadlines.
✨Prepare for Regulatory Discussions
Brush up on regulatory requirements related to the development and validation of analytical methods. Be ready to discuss your experience with compliance and how you've navigated regulatory challenges in previous roles.
