At a Glance
- Tasks: Test raw materials and finished products to ensure quality standards.
- Company: Join a leading pharmaceutical company with a commitment to excellence.
- Benefits: Competitive pay, potential for contract renewal, and valuable industry experience.
- Other info: Flexible shifts and opportunities for career growth in a dynamic environment.
- Why this job: Make a difference in healthcare by ensuring the quality of life-saving products.
- Qualifications: Degree in a scientific field and experience in analytical techniques required.
The predicted salary is between 17.18 - 17.18 £ per hour.
Opportunity
Are you currently working in analytical quality control?
Do you have hands‑on particle size analysis experience and analytical testing of raw materials, in‑process, release, and stability checks of drug products?
This role offers the chance to work for a large pharmaceutical company.
Role Overview
As a Quality Control Analytical Laboratory Analyst GMP/GLP based in Kent, you will test raw materials, finished products, in process controls and composite samples to GMP/GLP standards.
Key Responsibilities
- Perform routine particle size analysis (Malvern Mastersizers, Sympatec).
- Conduct cleaning verification using HPLC.
- Carry out identification testing with FTIR and Raman.
- Develop and validate methods, including particle size and cleanability assessments.
- Use DSC, light microscopy, SEM, Karl Fisher for moisture content.
- Optimize methods, troubleshoot, support technology transfer and pharmacopoeia analyses.
- Participate in CAPAs, deviations and document control.
- Working Hours
- Early shift: 6 a. m.–2 p. m., Monday–Friday (3 weeks, then changes).
- Late shift: 1:30 p. m.–10 p. m., Monday–Thursday; 1:30 p. m.–7 p. m., Friday (3 weeks, then changes).
- Night shift: 9 p. m.–7 a. m., Monday–Thursday (3 weeks, then back to early shift).
- Contract & Compensation
This is a 12‑month contract, potentially renewable or for permanent placement depending on performance. Pay is £17.18 per hour.
- Required Skills
- Degree or equivalent in a scientific subject.
- Experience in wet chemistry/analytical techniques, ideally within the pharmaceutical or related industry.
- Must be clean‑shaven; no makeup, false eyelashes or nail varnish due to clean‑room work.
EEO Statement
We are an equal opportunity employer and welcome applications from all qualified individuals.
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Quality Control Laboratory Analyst GMP / GLP – Kent in Erith employer: Quality Start
Join a dynamic team where your role as a Production Planner and Sales Operations Planner will be pivotal in ensuring the seamless delivery of customer orders. Our company fosters a collaborative work culture that prioritises employee growth, offering training and development opportunities to enhance your skills. Located in a vibrant area, we provide competitive pay and a supportive environment that values innovation and teamwork.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Control Laboratory Analyst GMP / GLP – Kent in Erith
✨Get Familiar with Temporary Roles in Pharma
Temporary positions in the pharmaceutical industry often arise during specific periods, like product launches or seasonal hiring sprints. Keep an eye on timelines and be proactive in reaching out to companies, especially around these busy times!
✨Join Pharma Networking Events
Participate in local and virtual pharmaceutical networking events or job fairs. This is a fantastic way to get in front of hiring managers and learn more about temporary opportunities directly from those in the know.
✨Leverage Your University Career Services
If you’re a student or recent grad, tap into your university’s career services which often have specific connections to pharma companies looking to fill temporary roles. They might even have exclusive internship programmes that lead to temp jobs!
✨Be Visible Online and Offline
Utilise platforms like LinkedIn to share your interests in temporary roles and connect with industry professionals. Plus, consider writing about relevant pharmaceutical topics to showcase your knowledge and enthusiasm—this can help you stand out to hiring companies like Quality Start.
We think you need these skills to ace Quality Control Laboratory Analyst GMP / GLP – Kent in Erith
Some tips for your application 🫡
Highlight Your Relevant Experience:In the pharmaceutical industry, it's crucial to showcase any relevant experience you have, whether it's internships, lab work, or coursework. Let’s emphasise your familiarity with drug development processes and any hands-on experience you've had with lab equipment or clinical trials in your CV.
Mention Certifications and Training:If you’ve got any certifications relevant to pharmaceuticals, like Good Clinical Practice (GCP) or a certification in pharmacovigilance, make sure to include them. These show your commitment to the field and can make a positive impact on your application for a temporary role at Quality Start.
Show Your Flexibility and Availability:Temporary positions often require immediate availability and flexibility in working hours. In your cover letter, make it clear when you can start and your ability to adapt to changing schedules, as this is key to a successful application.
Express Your Learning Goals:Since this is a temporary role, we suggest discussing what you hope to learn or gain from the experience at Quality Start. This not only shows your eagerness but also helps employers see you as someone who’s ready to make the most out of the opportunity.
How to prepare for a job interview at Quality Start
✨Know Your Regulations
In the pharmaceutical industry, it’s crucial to understand key regulations like GMP (Good Manufacturing Practices) or GCP (Good Clinical Practices). Brush up on these standards and be ready to discuss how they influence your work approach during your interview with Quality Start.
✨Emphasise Adaptability
Since this is a temporary role, show that you're ready to hit the ground running. Share examples from your past experiences that demonstrate your ability to adapt quickly to new environments or changes, especially in a fast-paced setting like pharmaceuticals.
✨Highlight Relevant Skills and Tools
Whether it’s laboratory techniques or software like LabWare or SAS, make sure you can confidently talk about your technical skills. If you have experience with any specific tools used in previous roles, relate that directly to how it can help Quality Start achieve its goals.
✨Prepare for Technical Questions
Be ready for technical questions related to drug development processes or quality assurance. We should expect scenarios where you might have to troubleshoot a problem or suggest improvements on a project—this shows your problem-solving capability in a temporary role.
