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- Tasks: Join our QC team to ensure top-notch quality in veterinary products through testing and compliance.
- Company: CK Group is a leading pharmaceutical organization based in Dundee, specializing in veterinary product development.
- Benefits: Enjoy a competitive salary, hands-on experience, and the chance to work in a dynamic lab environment.
- Why this job: Make a real impact in the pharmaceutical industry while honing your analytical skills in a supportive team.
- Qualifications: A degree in Chemistry or Biology and experience with HPLC/GC techniques are essential.
- Other info: This is a 6-month contract role with opportunities for professional growth.
The predicted salary is between 45000 - 55000 £ per year.
Job Title: QC Analyst We are seeking a highly skilled Quality Control (QC) Analyst to join our team at CK Group in Dundee. The successful candidate will work on a contract basis for 6 months within a Quality Control Laboratory for a leading pharmaceutical organisation that develops and manufactures veterinary products. Key Responsibilities: Adhere to Health and Safety practices and policies by reporting incidents, identifying risks, wearing PPE, and guiding others on HS&E best practices. Maintain quality and compliance through good housekeeping, GLP, GMP, and Data Integrity requirements, while guiding other team members to achieve these standards. Perform testing as trained to support department deliverables, including: Starting materials, finished products, and stability samples Non-routine and project testing/work Laboratory investigations for OOT/OOE/OOS Validation testing activities Support team leads by providing technical expertise and assistance to analysts. Raise and investigate OOS/OOT/OOE incidents. Assist in the closure of team actions related to CAPA/LIR/change control/audit actions and method updates. Your Background: You hold a degree or equivalent in a relevant scientific discipline such as Chemistry or Biology. You have experience as an analytical chemist with skills in chromatographic (HPLC and/or GC), spectroscopic, and classical techniques. You possess strong knowledge of GMP and Data integrity requirements in QC environments. You have excellent troubleshooting skills. You come from an industry background in a Pharmaceutical, Laboratory, or related environment. You are able to conduct laboratory investigations. You can review documents and testing reports. You are experienced in using Chromeleon Software. Requirements: Entitlement to work in the UK is essential. Salary: £45,000 – £55,000 per annum, depending on experience.
QC Analyst employer: CK Group
Contact Detail:
CK Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Analyst
✨Tip Number 1
Familiarize yourself with the specific quality control standards and regulations in the pharmaceutical industry, especially GMP and Data Integrity. This knowledge will not only help you during the interview but also demonstrate your commitment to maintaining high-quality standards.
✨Tip Number 2
Highlight any experience you have with chromatographic techniques like HPLC and GC. Be prepared to discuss specific projects or challenges you've faced using these methods, as this will showcase your technical expertise and problem-solving skills.
✨Tip Number 3
Since the role involves guiding other team members, think of examples where you've successfully led or trained others in a lab setting. This will illustrate your leadership abilities and your understanding of teamwork in a QC environment.
✨Tip Number 4
Make sure to brush up on your knowledge of Chromeleon Software, as it's specifically mentioned in the job description. Being able to discuss your proficiency with this software will give you an edge over other candidates.
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. Highlight key responsibilities and required skills, and think about how your experience aligns with these.
Tailor Your CV: Customize your CV to emphasize your relevant experience in quality control, analytical chemistry, and any specific techniques mentioned, such as HPLC or GC. Use keywords from the job description to make your application stand out.
Craft a Strong Cover Letter: Write a compelling cover letter that explains why you are a great fit for the QC Analyst role. Mention your background in pharmaceuticals, your understanding of GMP and Data Integrity, and your troubleshooting skills.
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 a QC role.
How to prepare for a job interview at CK Group
✨Know Your Technical Skills
Make sure to highlight your experience with chromatographic and spectroscopic techniques during the interview. Be prepared to discuss specific projects where you utilized HPLC or GC, as well as any troubleshooting experiences you've had.
✨Understand GMP and Data Integrity
Since the role emphasizes compliance with GMP and data integrity, familiarize yourself with these concepts. Be ready to explain how you've maintained quality standards in previous roles and how you ensure data integrity in your work.
✨Demonstrate Team Collaboration
The position requires guiding other team members and providing technical expertise. Share examples of how you've successfully collaborated with colleagues in a lab setting, especially in resolving OOS/OOT incidents or supporting CAPA actions.
✨Prepare for Behavioral Questions
Expect questions that assess your problem-solving abilities and how you handle challenges in a laboratory environment. Use the STAR method (Situation, Task, Action, Result) to structure your responses effectively.
