Sr. Scientist, Analytical Development and Quality Control in Newark on Trent

Sr. Scientist, Analytical Development and Quality Control in Newark on Trent

Newark on Trent Full-Time 160000 - 160000 £ / year (est.) No working from home possible
Proclinical

At a Glance

  • Tasks: Lead analytical development for innovative therapies and oversee external laboratories.
  • Company: Dynamic biotech company focused on transformative medicines.
  • Benefits: Competitive salary, bonus potential, equity options, and collaborative culture.
  • Other info: Opportunity for career growth and visibility across multiple development programmes.
  • Why this job: Make a real impact on patient outcomes with cutting-edge peptide therapeutics.
  • Qualifications: PhD or MSc in Analytical Chemistry with strong industry experience.

The predicted salary is between 160000 - 160000 £ per year.

Ready to play a pivotal role in bringing innovative therapies to patients while shaping analytical strategy across a growing late-stage biotech pipeline? Proclinical is working alongside a clinical-stage biotechnology company developing innovative medicines for serious diseases with significant unmet medical need. With multiple assets advancing through late-stage clinical development and strategic partnerships with major global pharmaceutical companies, the organisation is entering an exciting period of growth and portfolio expansion.

As part of a highly collaborative CMC organisation, the company is seeking a Senior Scientist, Analytical Development & Quality Control to provide analytical leadership across drug substance and drug product development programmes.

Primary Responsibilities:

  • This is an excellent opportunity for an experienced analytical scientist who enjoys combining hands-on scientific expertise with strategic programme leadership.
  • You will act as a key analytical subject matter expert, working across development stages to design analytical strategies, oversee external laboratories and ensure robust analytical control throughout the product lifecycle.
  • The role offers significant visibility across CMC, Regulatory Affairs, Quality, Manufacturing and Technical Operations teams, making it ideal for someone looking to broaden their impact within a fast-moving biotechnology environment.

Skills & Requirements:

  • PhD or MSc in Analytical Chemistry or a related scientific discipline
  • Strong pharmaceutical or biotechnology industry experience within Analytical Development
  • Expertise in UHPLC/HPLC method development and validation
  • Experience with LC-MS and advanced analytical characterisation techniques
  • Background supporting peptides, complex biologics, ADCs, proteins or related therapeutic modalities
  • Demonstrated experience managing external CDMOs or analytical service providers
  • Experience supporting CMC development programmes through multiple clinical stages
  • Understanding of GMP requirements, quality systems and regulatory expectations
  • Regulatory submission experience would be highly advantageous

The Sr. Scientist's responsibilities will be:

  • Lead analytical development activities for drug substance and drug product programmes
  • Develop, optimise and validate analytical methods using modern chromatographic and spectroscopic techniques
  • Design analytical control strategies, specifications and characterisation plans
  • Support stability studies, comparability assessments and impurity characterisation activities
  • Manage analytical testing and development activities at external CDMOs and CROs
  • Review analytical data and provide scientific guidance on investigations, deviations and troubleshooting activities
  • Support regulatory submissions including INDs, IMPDs and marketing applications
  • Collaborate closely with cross-functional teams across CMC, Quality and Regulatory functions
  • Contribute to continuous improvement initiatives and scientific best practice across the organisation

Compensation: $150,000 to $160,000 per annum.

Why Join?

  • Opportunity to work on innovative peptide therapeutics approaching key clinical and commercial milestones
  • Broad ownership and visibility across multiple development programmes
  • Exposure to both scientific and strategic CMC activities
  • Collaborative biotech culture with direct access to senior leadership
  • Strong compensation package including bonus and equity potential
  • Opportunity to contribute to medicines with the potential to transform patient outcomes

If you are having difficulty in applying or if you have any questions, please contact Neil Walton at (url removed).

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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Sr. Scientist, Analytical Development and Quality Control in Newark on Trent employer: Proclinical

Proclinical is an exceptional employer dedicated to advancing healthcare through innovative project management. With a strong focus on employee growth, we offer opportunities for professional development and the chance to work on impactful projects within NHS settings across the UK and Ireland. Our collaborative work culture fosters open communication and teamwork, making it a rewarding environment for those looking to make a meaningful difference in the life sciences sector.

Proclinical

Contact Details:

Proclinical Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Sr. Scientist, Analytical Development and Quality Control in Newark on Trent

Get Involved in Local Research Communities

Tap into local biotechnology meetups and research forums. These are great places to mingle with industry professionals, share your passion, and even discover unadvertised job openings. It's all about getting your face known in the field!

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Show Off Your Projects

Curate a portfolio showcasing any research projects or internships you've completed in biotechnology. This tangible evidence of your skills can really impress employers when you chat with them at networking events or interviews. It's about making that killer first impression!

Stay Up-to-Date with Industry Trends

Biotech is a fast-paced field, so keeping yourself updated with the latest advancements is crucial. Attend industry conferences, webinars, or workshops to broaden your knowledge and meet potential employers. Plus, it’ll give you fantastic talking points for your interviews at places like Proclinical!

We think you need these skills to ace Sr. Scientist, Analytical Development and Quality Control in Newark on Trent

Analytical Chemistry
UHPLC/HPLC Method Development
LC-MS
Analytical Characterisation Techniques
CDMO Management
GMP Requirements
Regulatory Submission Experience

Some tips for your application 🫡

Show Off Your Lab Skills:In the biotechnology field, it's super important to highlight your lab experience in your CV. Be sure to mention specific techniques or instruments you've mastered (think PCR, gel electrophoresis, etc.) and any relevant projects you've worked on. This will show Proclinical that you have the hands-on skills they need.

Tailor Your Technical Skills:Make sure to emphasise your technical skills, especially those relevant to the biotechnology sector. Include any software tools or programming languages you've used, like R or Python for data analysis, which could be key for this role at Proclinical.

Craft a Compelling Cover Letter:Since this is a full-time role, your cover letter should reflect not only your passion for biotechnology but also your long-term career ambitions. Share why you're excited about the work that Proclinical does and how you envision contributing to their goals. This shows that you’re not just looking for any job, but you're genuinely invested in this opportunity.

Include Your Papers and Projects:If you've published any papers or contributed to significant projects, mention them! These documents can boost your application and provide tangible evidence of your expertise in the biotechnology field. Don’t forget to link to any relevant publications or project summaries—this can set you apart from other candidates.

How to prepare for a job interview at Proclinical

Brush Up on Lab Techniques

Since you're eyeing a full-time gig in biotechnology, make sure you're well-versed in the lab techniques relevant to the role. Be ready to talk about PCR, CRISPR, or any specific methods mentioned in the job description at Proclinical. You might even be asked to demonstrate your understanding of these processes.

Know Your Bioinformatics Tools

Get comfortable with bioinformatics tools that are commonly used in the industry, like BLAST or Bioconductor. These are key in biotechnology, and having hands-on experience or at least familiarity can set you apart. Prepare to discuss any relevant projects you've worked on, especially if they involved data analysis or genomic research.

Show Your Teamwork Skills

Biotech often involves collaboration across multiple disciplines. Be ready to share stories that highlight your teamwork and communication skills, especially in research projects. Think about working with different teams at university or any internships – this is where you can show how well you fit into Proclinical's culture.

Research Recent Biotech Innovations

Stay updated on the latest trends and breakthroughs in biotechnology. Knowing what's happening in the field can help you engage in more meaningful discussions during your interview. Bring up recent articles or advancements that excite you, especially those related to the work being done at Proclinical. This shows your passion for the industry!