Quality Control Analyst in Sunderland

Quality Control Analyst in Sunderland

Sunderland Full-Time 30000 - 40000 £ / year (est.) No working from home possible
Curaleaf International

At a Glance

  • Tasks: Conduct precise testing and analysis to ensure product quality and safety.
  • Company: Join Curaleaf International, a leader in the cannabis industry with a commitment to excellence.
  • Benefits: Enjoy competitive salary, generous holiday, private medical insurance, and free parking.
  • Other info: Full training provided and opportunities for professional development in a collaborative team.
  • Why this job: Make a real impact in a fast-growing, purpose-driven organisation focused on patient care.
  • Qualifications: Degree in Life Sciences or Chemistry preferred; relevant experience considered.

The predicted salary is between 30000 - 40000 £ per year.

Location: Sunderland, UK

Industry: Pharmaceutical / Regulated Manufacturing

Type: Full-time on site

Role Overview

We are seeking a detail‑oriented Quality Control Analyst to join our laboratory team, delivering accurate, compliant testing that underpins the safety and quality of our raw materials and finished products. You will perform chromatographic and wet chemistry analysis aligned with pharmacopoeia standards, support method development, and uphold GMP/GDP requirements across all activities. If you thrive in a precise, regulated environment and want to grow your technical expertise, this is the ideal role for you.

Key Responsibilities

  • Manage laboratory reagents and consumables to ensure uninterrupted testing workflows
  • Operate, calibrate, and maintain all lab equipment in strict compliance with GMP, GDP, and Health & Safety standards
  • Review raw material documentation from suppliers to confirm suitability for manufacturing use
  • Perform comprehensive testing of raw materials and finished products, including HPLC, FTIR, and wet chemistry techniques, to support approval processes
  • Conduct analytical method transfers and development activities following approved protocols and under the guidance of the Quality team
  • Support stability programmes through timely sample pull‑point management and analysis
  • Author laboratory reports and technical documents for method development and transfer
  • Oversee raw material purchasing, handling, sampling, and final approval
  • Collaborate with Production teams to prioritise and schedule manufacturing in line with quality requirements
  • Complete mandatory training and pursue ongoing professional development
  • Represent the company professionally with suppliers, clients, and internal stakeholders
  • Adhere fully to HR policies, Health & Safety regulations, and strict confidentiality requirements
  • Work flexibly to meet business needs while maintaining the highest professional standards

Skills & Specifications

  • Practical knowledge of High Performance Liquid Chromatography (HPLC) and core analytical chemistry laboratory techniques
  • Strong proficiency in Microsoft Office suite
  • Highly organised, with the ability to maintain accurate, contemporaneous records compliant with ALCOA+ principles
  • Inquisitive, solution‑focused mindset; skilled at systematic problem‑solving and root‑cause analysis
  • Bachelor's degree (or higher) in Life Sciences, Chemistry, or a related discipline is preferred – relevant equivalent experience will also be considered

What We Offer

  • Competitive salary
  • 27 days annual holiday + 8 bank holidays
  • Private medical insurance
  • Free on-site parking

Why Join Curaleaf?

  • Work within a fast‑growing, purpose‑driven organisation
  • Play a key role in shaping how patients access information and support
  • Full training provided on regulatory requirements
  • Be part of a collaborative team supporting accessible medical care
Curaleaf International

Contact Details:

Curaleaf International Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Quality Control Analyst in Sunderland

Unlock Networking Opportunities

Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Curaleaf International. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.

Join Relevant Professional Bodies

Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Curaleaf International.

Leverage Internships for Full-time Roles

If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Curaleaf International. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.

Tailor Your Approach

When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Curaleaf International is looking for. A tailored application can really make you stand out!

We think you need these skills to ace Quality Control Analyst in Sunderland

Chromatographic Analysis
Wet Chemistry Techniques
High Performance Liquid Chromatography (HPLC)
Fourier Transform Infrared Spectroscopy (FTIR)
GMP Compliance
GDP Compliance
Analytical Method Development

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Curaleaf International!

Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Curaleaf International that you're not just a fit for the job but also a safety-conscious candidate!

Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Curaleaf International!

Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Curaleaf International, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.

How to prepare for a job interview at Curaleaf International

Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Curaleaf International that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

Showcase Relevant Experience

If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.

Know Their Products

Take some time to familiarise yourself with Curaleaf International’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.

Be Ready for Regulatory Scenarios

In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.