Senior Analytical Scientist

Senior Analytical Scientist

Macclesfield Temporary
T

At a Glance

  • Tasks: Lead analytical development for early clinical drug products and conduct lab experiments.
  • Company: Join a dynamic team focused on innovative drug development and patient safety.
  • Benefits: Enjoy free payroll, dedicated support, and timely payments with ongoing training.
  • Why this job: Make a real impact in healthcare while developing your skills in a supportive environment.
  • Qualifications: BSc, MSc, PhD in Chemistry or Analytical Chemistry required; experience in pharmaceuticals preferred.
  • Other info: Diversity and inclusion are core values; we offer training on unconscious bias.
  • Lead the analytical development activities to support development and supply of drug product during the early clinical phases.

  • Identify and develop the analytical methodologies that support project progression through early development.

  • Conduct lab-based experimental work to generate data to support progression of your own and other projects. This will include compliance with Good Manufacturing Practice where appropriate.

  • Author the relevant sections of regulatory submissions and prepare responses to regulatory questions.

  • Interpret analytical data and draw reliable conclusions and recommendations to influence project progression.

  • Develop the risk assessments and stability and control strategies that ensure our patients receive a safe and efficacious drug product., As a CK contractor you will have your own dedicated consultant who will make sure that you receive:

  • Free payroll

  • A face-to-face induction at the start of your contract

  • A new starter pack

  • Training on how to submit your timesheets

  • Ongoing support from our accounts and payroll team to make sure you get paid correctly and on time

  • Provided that you submit your timesheets on time – you will always be paid on time

  • Access to your own timesheet and payment records securely hosted on our system

  • Regular contact both face-to -face and on the phone from CK

  • Ongoing appraisal and support system

  • Access to our refer a friend scheme

  • CK monthly newsletter

  • Support at the end of your contract/placement to find you the next role

Diversity and Inclusion:

We are part of the REC Diversity Pledge and the BITC Race at Work Charter. We also provide all our staff with VISA and Unconscious Bias training. We are conscious in our internal and external recruitment to consciously follow our pledges.

  • A BSc, MSc, PhD or equivalent in Chemistry or Analytical Chemistry.

  • An understanding of analytical science inputs into early phase drug product development and clinical supply (for example risk assessment, stability strategy, control strategy).

  • An understanding of analytical techniques used to characterise drug products in early phase development and for clinical supply.

  • Experience in the pharmaceutical or similar research or manufacturing industry.

  • Experience of authoring CMC content for the analytical aspects of drug product regulatory filings (desirable).

Hourly: £26.00 PAYE or £50.68 Umbrella – this role is inside IR35.

Senior Analytical Scientist employer: The CK Group Inc

At CK, we pride ourselves on being an exceptional employer, offering a supportive work culture that prioritizes employee growth and development. As a Senior Analytical Scientist, you will benefit from dedicated consultancy support, comprehensive training, and a commitment to diversity and inclusion, ensuring you thrive in your role while contributing to meaningful drug development. Our focus on compliance and innovation, combined with ongoing appraisal systems, makes CK a rewarding place to advance your career in the pharmaceutical industry.
T

Contact Detail:

The CK Group Inc Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Analytical Scientist

✨Tip Number 1

Make sure to highlight your experience with analytical methodologies in your conversations. Discuss specific techniques you've used and how they contributed to project progression, as this will resonate well with the role's requirements.

✨Tip Number 2

Familiarize yourself with Good Manufacturing Practice (GMP) standards. Being able to discuss how you have adhered to these practices in previous roles will demonstrate your readiness for compliance in this position.

✨Tip Number 3

Prepare to discuss your experience with regulatory submissions. Be ready to share examples of how you've authored sections or responded to regulatory questions, as this is a key aspect of the job.

✨Tip Number 4

Showcase your ability to interpret analytical data effectively. Think of instances where your conclusions influenced project decisions, as this will illustrate your analytical thinking and problem-solving skills.

We think you need these skills to ace Senior Analytical Scientist

Analytical Method Development
Good Manufacturing Practice (GMP)
Regulatory Submission Authoring
Data Interpretation
Risk Assessment
Stability Strategy Development
Control Strategy Development
Experimental Design
Pharmaceutical Industry Experience
Analytical Techniques Proficiency
Project Progression Influence
Attention to Detail
Communication Skills
Team Collaboration

Some tips for your application 🫡

Understand the Role: Make sure to thoroughly read the job description for the Senior Analytical Scientist position. Highlight key responsibilities and required qualifications, such as experience in analytical methodologies and regulatory submissions.

Tailor Your CV: Customize your CV to reflect your relevant experience in analytical chemistry and drug product development. Emphasize any specific projects or roles that align with the responsibilities mentioned in the job description.

Craft a Strong Cover Letter: Write a compelling cover letter that connects your background to the role. Discuss your understanding of analytical techniques and how your experience can contribute to the company's goals in early phase drug development.

Highlight Compliance Experience: If you have experience with Good Manufacturing Practice (GMP) or regulatory submissions, make sure to highlight this in your application. This is crucial for demonstrating your fit for the role.

How to prepare for a job interview at The CK Group Inc

✨Showcase Your Analytical Expertise

Be prepared to discuss your experience with analytical methodologies and how they have supported project progression in early drug development. Highlight specific techniques you've used and the outcomes of your work.

✨Understand Regulatory Requirements

Familiarize yourself with the regulatory submission process, especially regarding CMC content. Be ready to explain how you have authored relevant sections in the past and how you would approach regulatory questions.

✨Demonstrate Problem-Solving Skills

Prepare examples of how you've interpreted analytical data to draw conclusions that influenced project decisions. Discuss any challenges you faced and how you overcame them, particularly in compliance with Good Manufacturing Practice.

✨Emphasize Team Collaboration

Since this role involves working on multiple projects, be ready to talk about your experience collaborating with cross-functional teams. Share how you communicate findings and strategies effectively to ensure project success.

Senior Analytical Scientist
The CK Group Inc Apply now
T
  • Senior Analytical Scientist

    Macclesfield
    Temporary
    Apply now

    Application deadline: 2026-12-13

  • T

    The CK Group Inc

  • Other open positions at The CK Group Inc

    T
    Lead Cyber security Analyst

    The CK Group Inc

    Full-Time 48000 - 84000 £ / year (est.)
Similar positions in other companies
R
Analytical Scientist (R&D)

RBW Consulting

Cardiff Full-Time 36000 - 60000 £ / year (est.)
C
Materials Analyst – Chemistry

CV-Library

London Full-Time 20800 - 26000 £ / year (est.)
Europas größte Jobbörse für Gen-Z
discover-jobs-cta
Discover now
>