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- Tasks: Join us as a QC Analyst to ensure top-notch quality in our lab!
- Company: Be part of a global leader in healthcare, dedicated to improving lives.
- Benefits: Earn £17.18 per hour with a 25% shift allowance and flexible shifts.
- Why this job: Make a real impact in healthcare while gaining valuable lab experience.
- Qualifications: Science degree required; lab experience in a cGXP environment preferred.
- Other info: This role involves a 12-month contract and may require a DBS check.
CK Group are recruiting for a Quality Control Analyst, to join a global healthcare provider to hospitals, clinics and homes, based in Dartford, on a contract basis for 12 months. 74 per hour + 25% shift allowance = £17.18 per hour . Shift based roles, 3 weeks rotation. Early shift 6am – 2pm Monday-Friday, Late shift 1:30pm – 10pm Monday-Thursday, 1:30pm – 7pm Friday Night shift, 9pm – 7am Monday – Thursday. Quality Control Analyst Role: Ensure all tasks are conducted in accordance with defined Risk & COSHH assessments. To support identification, reporting and implementation of EHS improvement within the QC laboratory via Entropy in alignment with management. To identify and trigger a laboratory investigation, deviation, CAPA or change control under the supervision of a more senior analyst. Perform analytical testing in an accurate, timely and efficient manner, consistent with cGMP requirements. Oracle, Word, Excel, Trackwise, Compliance, Wire, Minitab. Science graduate or higher with proven experience of laboratory operation in a cGXP environment or extensive industry experience. Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives. This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
QC Analyst - Pharma employer: CK Group
Contact Detail:
CK Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Analyst - Pharma
✨Tip Number 1
Familiarize yourself with cGMP requirements and the specific analytical testing methods used in the pharmaceutical industry. This knowledge will not only help you during the interview but also demonstrate your commitment to quality control.
✨Tip Number 2
Highlight any experience you have with tools like Oracle, Minitab, or Trackwise. Being proficient in these systems can set you apart from other candidates and show that you're ready to hit the ground running.
✨Tip Number 3
Prepare to discuss your experience with risk assessments and EHS improvements. Be ready to provide examples of how you've contributed to safety and compliance in previous roles.
✨Tip Number 4
Since this role involves shift work, be sure to express your flexibility and willingness to adapt to different schedules. Employers appreciate candidates who can seamlessly integrate into their operational needs.
We think you need these skills to ace QC Analyst - Pharma
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Quality Control Analyst position. Understand the key responsibilities, required skills, and the importance of compliance with cGMP requirements.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in laboratory operations within a cGXP environment. Mention specific analytical testing methods you are familiar with and any relevant software tools like Oracle, Minitab, or Trackwise.
Tailor Your Application: Customize your application materials to reflect the values and goals of the healthcare provider. Show how your background aligns with their mission of putting patients first and improving health outcomes.
Proofread Your Documents: Before submitting your application, carefully proofread your CV and cover letter for any errors or typos. A polished application demonstrates attention to detail, which is crucial for a Quality Control Analyst.
How to prepare for a job interview at CK Group
✨Understand cGMP Requirements
Make sure you have a solid understanding of current Good Manufacturing Practices (cGMP). Be prepared to discuss how you've applied these principles in your previous roles, as this will demonstrate your readiness for the Quality Control Analyst position.
✨Familiarize Yourself with Relevant Software
Since the role requires knowledge of Oracle, Word, Excel, Trackwise, Compliance, Wire, and Minitab, brush up on these tools. Be ready to provide examples of how you've used them in past laboratory operations or data analysis.
✨Highlight Your Problem-Solving Skills
The job involves identifying and triggering laboratory investigations and CAPAs. Prepare to share specific instances where you've successfully resolved issues in a lab setting, showcasing your analytical and critical thinking skills.
✨Show Commitment to Safety and Compliance
Given the emphasis on Risk & COSHH assessments, be prepared to discuss your approach to safety and compliance in the laboratory. Share any experiences where you contributed to EHS improvements or adhered to safety protocols.
