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- Tasks: Join our QC team to ensure top-notch quality control of pharmaceutical products.
- Company: A leading pharmaceutical company known for its success and innovation.
- Benefits: Enjoy a 4-day work week with competitive salary and comprehensive benefits.
- Why this job: Be part of a collaborative environment that values precision and attention to detail.
- Qualifications: Degree in chemistry or related field; experience in analytical testing preferred.
- Other info: Work hours are Tuesday to Friday, 07:30 to 16:45.
The predicted salary is between 36000 - 60000 £ per year.
Our Client is a very successful pharmaceutical company. They are now seeking a QC Analyst . This position is a full-time permanent role and will be based near Hitchin, Hertfordshire. Our Client operates a 4 day week. The hours will be Tuesday to Friday 07.30 to 16.45. Job Purpose An opportunity has arisen for an Analyst to join an existing QC team within the Pharmaceutical Development and Support (PDS) department. Key Areas of Responsibility Carry out the Quality Control of raw materials, bulk and finished products in accordance with relevant authorised documentation using HPLC, GC and wet chemical techniques. Perform swabbing and analysis of samples for cleaning verification of the pilot production facility. Take equal part in the overall running of the laboratory, including equipment maintenance, calibration of apparatus and other general duties such as solvent disposal. Perform manual and automated tests and assays in accordance with GMP to a high level of accuracy and precision and to operate associated analytical equipment. Qualifications / Experience Some relevant experience in an analytical testing role, preferably in a GMP environment. (This experience could include an industrial placement year). Some experience in the techniques of HPLC and GC analysis. Excellent attention to detail and organisational skills and the ability to self-motivate under your own initiative. Collaborative skills to work closely with colleagues and managers. Use of software packages, such as Chromatography Data Handling, LIMS and Excel, for the collection, processing and reporting of data. In return, our client is offering a competitive basic salary plus comprehensive benefits for the successful Candidate. Please send your C.V to Lorraine Roger, Director at Atom Recruitment Ltd. #J-18808-Ljbffr
QC Analyst employer: Atom Recruitment
Contact Detail:
Atom Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Analyst
✨Tip Number 1
Familiarize yourself with the specific analytical techniques mentioned in the job description, such as HPLC and GC. Consider taking online courses or certifications to enhance your knowledge and demonstrate your commitment to mastering these skills.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those working in quality control. Attend industry events or join relevant online forums to connect with potential colleagues and learn more about the company culture.
✨Tip Number 3
Highlight any experience you have in a GMP environment during your conversations or interviews. Be prepared to discuss specific examples of how you've maintained quality standards and ensured compliance in previous roles.
✨Tip Number 4
Showcase your attention to detail and organizational skills by preparing for the interview with a clear plan. Bring examples of how you've successfully managed multiple tasks or projects, particularly in a laboratory setting.
We think you need these skills to ace QC Analyst
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the QC Analyst position. Understand the key responsibilities and required qualifications, especially the importance of GMP compliance and analytical techniques like HPLC and GC.
Tailor Your CV: Customize your CV to highlight relevant experience in analytical testing and any specific skills related to HPLC and GC analysis. Emphasize your attention to detail and organizational skills, as these are crucial for the role.
Craft a Strong Cover Letter: Write a compelling cover letter that explains why you are a great fit for the QC Analyst position. Mention your educational background in chemistry and any relevant experience in a GMP environment. Show enthusiasm for the opportunity to work in a collaborative team.
Proofread Your Application: Before submitting your application, carefully proofread your CV and cover letter. Check for any spelling or grammatical errors, and ensure that all information is accurate and clearly presented.
How to prepare for a job interview at Atom Recruitment
✨Know Your Techniques
Make sure you are well-versed in HPLC and GC analysis techniques. Be prepared to discuss your experience with these methods and how you've applied them in previous roles.
✨Demonstrate Attention to Detail
Since the role requires excellent attention to detail, be ready to provide examples of how you've ensured accuracy and precision in your past work, especially in a GMP environment.
✨Show Your Collaborative Spirit
Highlight your ability to work as part of a team. Prepare examples of how you've successfully collaborated with colleagues and managers in previous positions.
✨Familiarize Yourself with Relevant Software
Brush up on your knowledge of software packages like Chromatography Data Handling, LIMS, and Excel. Be ready to discuss how you've used these tools for data collection and reporting.
