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- Tasks: Join a QC team to ensure quality control of pharmaceutical products using advanced techniques.
- Company: A leading pharmaceutical company known for its innovative approach and success in the industry.
- Benefits: Enjoy a 4-day work week, competitive salary, and comprehensive benefits package.
- Why this job: Be part of a collaborative environment that values precision and attention to detail in impactful work.
- Qualifications: Relevant experience in analytical testing, preferably in a GMP setting, with skills in HPLC and GC.
- Other info: Work hours are Tuesday to Friday, 07:30 to 16:45, promoting a great work-life balance.
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
Contact Detail:
Atom Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Analyst
✨Tip Number 1
Familiarise yourself with the specific analytical techniques mentioned in the job description, such as HPLC and GC. Consider reaching out to professionals in the field or joining relevant online forums to gain insights and tips on best practices.
✨Tip Number 2
Highlight your experience in a GMP environment during any networking opportunities. Attend industry events or webinars where you can connect with others in the pharmaceutical sector, as personal connections can often lead to job referrals.
✨Tip Number 3
Demonstrate your attention to detail and organisational skills by preparing examples of how you've successfully managed projects or tasks in the past. Be ready to discuss these experiences in interviews to showcase your suitability for the role.
✨Tip Number 4
Make sure to research the company culture and values of the pharmaceutical company you're applying to. Tailor your conversations and questions during interviews to reflect your understanding of their mission and how you can contribute to their team.
We think you need these skills to ace QC Analyst
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in analytical testing, particularly in a GMP environment. Emphasise your familiarity with HPLC and GC techniques, as well as any software packages you've used like Chromatography Data Handling or LIMS.
Craft a Strong Cover Letter: Write a cover letter that showcases your attention to detail and organisational skills. Mention specific examples of how you've successfully collaborated with colleagues in previous roles, and express your enthusiasm for the QC Analyst position.
Highlight Relevant Skills: In your application, clearly outline your skills related to quality control processes, equipment maintenance, and data reporting. Use bullet points to make this information easy to read and ensure it aligns with the job description.
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 for a QC Analyst role.
How to prepare for a job interview at Atom Recruitment
✨Know Your Techniques
Make sure you brush up on your knowledge of HPLC and GC analysis techniques. Be prepared to discuss your experience with these methods and how you've applied them in previous roles, especially in a GMP environment.
✨Demonstrate Attention to Detail
As a QC Analyst, attention to detail is crucial. During the interview, provide examples of how you've ensured accuracy and precision in your work. This could include specific instances where your meticulousness made a difference in outcomes.
✨Show Your Collaborative Spirit
This role requires working closely with colleagues and managers. Be ready to share experiences that highlight your ability to collaborate effectively within a team. Discuss how you’ve contributed to team success in past positions.
✨Familiarise Yourself with Software Tools
Since the role involves using software like Chromatography Data Handling, LIMS, and Excel, it’s important to demonstrate your proficiency with these tools. Prepare to discuss how you've used similar software in your previous roles to manage data collection and reporting.
