At a Glance
- Tasks: Conduct hands-on testing of raw materials and drug products to ensure quality standards.
- Company: Join a leading pharmaceutical company with a commitment to innovation.
- Benefits: Competitive pay, flexible shifts, and potential for contract extension or permanent position.
- Other info: Dynamic work environment with opportunities for professional growth and development.
- Why this job: Make a real difference in healthcare by ensuring the quality of life-saving products.
- Qualifications: Experience in analytical quality control and familiarity with GMP/GLP standards.
The predicted salary is between 30000 - 40000 € per year.
Are you currently working in analytical quality control? Does your experience include hands-on particle size analysis, analytical testing of Raw Materials, In-process, Release and Stability checks of drug products? Want to work for a large pharmaceutical company? Yes then this is the role for you!
Your role as a Quality Control Analytical Laboratory Analyst GMP/GLP based in Kent will involve testing raw materials, finished products, in process controls and composite samples to GMP / GLP standards. Testing techniques may include, but are not limited to:
- Routine particle size analysis (Malvern Mastersizers, Sympatec)
- Cleaning verification (HPLC)
- Identification testing (FTIR and Raman)
- Method development and validation (including particle size and cleanability assessments)
- DSC
- Light microscopy
- SEM
- Moisture content (Karl Fisher)
- Method optimisation and troubleshooting
- Technology transfer
- Pharmacopoeia analyses
You will also get involved in CAPA's, deviations and document control.
The hours of work are:
- Early shift 6am - 2pm Monday-Friday for 3 weeks
- Late shift 1.30pm - 10pm Monday-Thursday, 1.30pm - 7pm Friday for 3 weeks
- Night shift 9pm - 7am Monday - Thursday for 3 weeks then back to the early shift.
This is a 12 months contract which will be reviewed for a possible extension or go permanent.
Quality Control Laboratory Analyst GMP / GLP - Kent employer: Quality Start
Join a leading pharmaceutical company in Kent, where you will thrive in a dynamic work culture that prioritises innovation and quality. With a strong commitment to employee development, you will have access to extensive training opportunities and career progression pathways, ensuring your growth in the field of analytical quality control. Enjoy competitive benefits and a supportive environment that values teamwork and excellence in delivering high-quality products.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Control Laboratory Analyst GMP / GLP - Kent
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work in quality control. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your technical skills. Make sure you can confidently discuss particle size analysis and other testing techniques mentioned in the job description. We want you to shine!
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your career goals. Check out our website for roles that match your skills in GMP/GLP environments. We’ve got your back!
✨Tip Number 4
Follow up after interviews! A quick thank-you email can keep you top of mind for hiring managers. It shows your enthusiasm and professionalism, which is always a plus in the competitive pharma world.
We think you need these skills to ace Quality Control Laboratory Analyst GMP / GLP - Kent
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your experience in analytical quality control and the specific techniques mentioned in the job description. We want to see how your skills match up with what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about quality control and how your background makes you a great fit for our team. Keep it engaging and relevant to the role.
Showcase Relevant Experience:When detailing your previous roles, focus on your hands-on experience with particle size analysis and other testing methods. We love seeing concrete examples of how you've tackled similar challenges in the past.
Apply Through Our Website:Don't forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at Quality Start
✨Know Your Techniques
Make sure you brush up on the specific testing techniques mentioned in the job description, like particle size analysis and HPLC. Be ready to discuss your hands-on experience with these methods and how you've applied them in previous roles.
✨Understand GMP/GLP Standards
Familiarise yourself with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Being able to articulate how you’ve adhered to these standards in your past work will show that you’re a serious candidate who understands the importance of compliance.
✨Prepare for Scenario Questions
Expect questions about how you would handle CAPAs, deviations, or document control issues. Think of specific examples from your experience where you successfully navigated similar challenges, as this will demonstrate your problem-solving skills.
✨Show Flexibility with Shifts
Since the role involves rotating shifts, be prepared to discuss your availability and willingness to adapt. Highlight any previous experience you have with shift work and how you managed your time effectively during those periods.
