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- Tasks: Conduct analytical testing on raw materials and drug products to ensure quality standards.
- Company: Join a leading pharmaceutical company dedicated to innovation and quality in healthcare.
- Benefits: Enjoy competitive pay, flexible shifts, and potential for contract extension or permanent position.
- Why this job: Gain hands-on experience in a dynamic lab environment while contributing to impactful healthcare solutions.
- Qualifications: A degree in a scientific field and experience in analytical techniques are essential.
- Other info: Opportunity for referral bonuses and various incentive schemes available.
Quality Control Laboratory Analyst GMP / GLP – Kent Opportunity: 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 is 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 trouble-shooting, technology transfer and 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 then it changes to * Late shift 1.30pm – 10pm Monday-Thursday, 1.30pm – 7pm Friday for 3 weeks then it changes to * Night shift 9pm – 7am Monday – Thursday for 3 weeks then back to the early shift. This is a 6 months contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate is £17.18 per hour. Skills: To apply for the Quality Control Analytical Laboratory Analyst GMP / GLP role you will have the following skills: * Degree or equivalent in a scientific subject. * Experience in wet chemistry / analytical techniques ideally within the pharmaceutical or related industry. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don’t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role
Quality Control Laboratory Analyst GMP / GLP employer: Quality Start
Contact Detail:
Quality Start Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Control Laboratory Analyst GMP / GLP
✨Tip Number 1
Familiarise yourself with the specific analytical techniques mentioned in the job description, such as particle size analysis and HPLC. Being able to discuss your hands-on experience with these methods during an interview will demonstrate your suitability for the role.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who work in quality control. Attend relevant conferences or workshops where you can meet potential colleagues and learn more about the latest trends and technologies in GMP/GLP standards.
✨Tip Number 3
Prepare to discuss your experience with CAPA’s and document control processes. These are crucial aspects of the role, and showing that you understand their importance will set you apart from other candidates.
✨Tip Number 4
Be ready to demonstrate your flexibility regarding shift patterns. Since the role involves rotating shifts, expressing your willingness to adapt to different working hours can make you a more attractive candidate.
We think you need these skills to ace Quality Control Laboratory Analyst GMP / GLP
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in analytical quality control, particularly with techniques mentioned in the job description such as particle size analysis and HPLC. Use specific examples to demonstrate your skills.
Craft a Strong Cover Letter: Write a cover letter that directly addresses the requirements of the Quality Control Laboratory Analyst role. Mention your degree, relevant experience, and why you are interested in working for a large pharmaceutical company.
Highlight Relevant Skills: In your application, emphasise your experience with GMP/GLP standards and any specific analytical techniques you have used. This will show that you are well-prepared for the responsibilities of the role.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in quality control roles.
How to prepare for a job interview at Quality Start
✨Know Your Techniques
Familiarise yourself with the specific analytical techniques mentioned in the job description, such as particle size analysis and HPLC. Be prepared to discuss your hands-on experience with these methods and how you've applied them in previous roles.
✨Understand GMP/GLP Standards
Make sure you have a solid understanding of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Be ready to explain how you have adhered to these standards in your past work, as this is crucial for the role.
✨Prepare for Scenario Questions
Expect scenario-based questions related to CAPAs, deviations, and document control. Think of examples from your experience where you successfully managed these situations and be ready to share them during the interview.
✨Show Your Team Spirit
Since the role involves working shifts and possibly collaborating with different teams, highlight your ability to work well in a team environment. Share examples of how you've contributed to team success in previous positions.