Analytical Scientist – GMP QC & HPLC Specialist (Flexible Hours)

Analytical Scientist – GMP QC & HPLC Specialist (Flexible Hours)

Full-Time 30000 - 40000 £ / year (est.) Home office (partial)
Eurofins

At a Glance

  • Tasks: Conduct routine and non-routine testing of pharmaceutical products using advanced analytical techniques.
  • Company: Join Eurofins PSS, a leader in analytical support with a flexible work culture.
  • Benefits: Enjoy flexible hours, a permanent position, and a supportive team environment.
  • Why this job: Make a difference in the pharmaceutical industry while honing your analytical skills.
  • Qualifications: Experience with HPLC and GMP-compliant data handling is essential.

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

Eurofins PSS is recruiting for Analytical Scientists to provide on-site analytical support as a Eurofins Managed PSS Scientist.

This is a permanent full-time position with a 35-hour week, flexibly scheduled between 7am and 7pm on 5/7 days as per business needs.

The role involves routine and non-routine testing of pharmaceutical products using HPLC, Dissolution, Karl Fischer and UV, with GMP-compliant data handling and collaboration with client teams.

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Analytical Scientist – GMP QC & HPLC Specialist (Flexible Hours) employer: Eurofins

Eurofins in Livingston, Scotland is an excellent employer that prioritises employee well-being and professional growth. With a supportive work culture, enhanced annual leave, a robust pension plan, and comprehensive health programs, employees are encouraged to thrive both personally and professionally. The opportunity to lead in a dynamic environment while contributing to meaningful projects makes Eurofins a rewarding place to advance your career.

Eurofins

Contact Details:

Eurofins Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Analytical Scientist – GMP QC & HPLC Specialist (Flexible Hours)

Unlock Networking Opportunities

Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Eurofins. 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 Eurofins.

Leverage Internships for Full-time Roles

If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Eurofins. 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 Eurofins is looking for. A tailored application can really make you stand out!

We think you need these skills to ace Analytical Scientist – GMP QC & HPLC Specialist (Flexible Hours)

HPLC
GMP Compliance
Analytical Testing
Dissolution Testing
Karl Fischer Analysis
UV Spectroscopy
Data Handling

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 Eurofins!

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 Eurofins 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 Eurofins!

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 Eurofins, 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 Eurofins

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 Eurofins 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 Eurofins’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.