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- Tasks: Conduct analytical testing and ensure quality control of veterinary products.
- Company: Join a leading pharmaceutical organisation focused on developing veterinary solutions.
- Benefits: Contract role with hands-on experience in a dynamic lab environment.
- Why this job: Gain valuable skills in a reputable company while contributing to animal health.
- Qualifications: Degree in Chemistry or Biology; experience with HPLC/GC techniques required.
- Other info: 3+ month contract based in Dundee; must be eligible to work in the UK.
CK Group are recruiting for a QC Analyst, to work within a Quality Control Laboratory, for a leading pharmaceutical organisation that develop and manufacture veterinary products.
The QC Analyst will be working on site in Dundee, on a contract basis for 6 months.
Key Responsibilities
- Perform analytical testing of raw materials, product packaging and final product to support the release, stability and in process testing of materials for production or products for commercial use.
- Accurately follow relevant SOPs, performing all activities in accordance with cGMP requirements, reporting anomalies. Initiate and complete laboratory discrepancy events on time.
- Document test results to ensure completeness and accuracy per cGMP, keeping accurate documentation.
- Demonstrate hands‑on knowledge of operating, maintenance and troubleshooting skills for HPLC instruments as well as quality / regulatory requirements pertinent to quality control environments / laboratories.
- Performing moderate to complex equipment / instrumentation troubleshooting.
- Contribute towards the development and revision of SOPs, investigations, the preparation laboratory investigation reports and implement corrective & preventative actions (CAPAs).
- Support departmental improvement projects related to release goals, the identification of root cause for investigations and the improvement of laboratory methods.
Your Background
- Educated to degree level or equivalent in a relevant scientific discipline such as Chemistry or Biology.
- Experienced analytical chemist with experience in chromatographic (HPLC and or GC) techniques.
- Strong knowledge of GMP and Data integrity requirements in QC environments.
- Strong troubleshooting skills.
- Industry background in a Pharmaceutical, Laboratory or related environment.
- Ability to conduct Laboratory investigations.
- Experienced with chromatography systems & software such as Chromeleon Software.
Apply
It is essential all applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.
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QC Analyst employer: CK Group- Science, Clinical and Technical
Contact Detail:
CK Group- Science, Clinical and Technical 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, particularly HPLC and GC. Being able to discuss your hands-on experience with these methods during an interview will demonstrate your suitability for the role.
✨Tip Number 2
Brush up on your knowledge of cGMP and data integrity requirements. Understanding these regulations is crucial for a QC Analyst, and being able to articulate how you've applied them in past roles can set you apart from other candidates.
✨Tip Number 3
Prepare to discuss any previous experience you have with laboratory investigations and CAPAs. Highlighting your problem-solving skills and ability to contribute to departmental improvement projects will show that you're proactive and results-oriented.
✨Tip Number 4
Network with professionals in the pharmaceutical industry, especially those who work in quality control. Engaging with others in the field can provide valuable insights and potentially lead to referrals, increasing your chances of landing the job.
We think you need these skills to ace QC Analyst
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the QC Analyst position. Understand the key responsibilities and required qualifications, especially the importance of cGMP compliance and analytical testing.
Tailor Your CV: Customise your CV to highlight relevant experience in analytical chemistry, particularly with HPLC and GC techniques. Emphasise your knowledge of GMP and data integrity, as well as any troubleshooting skills you possess.
Craft a Strong Cover Letter: Write a compelling cover letter that connects your background in Chemistry or Biology to the specific requirements of the QC Analyst role. Mention your hands-on experience with laboratory investigations and your ability to contribute to departmental improvement projects.
Double-Check Your Application: Before submitting your application, review all documents for accuracy and completeness. Ensure that you have included the job reference number in your correspondence and that your entitlement to work in the UK is clearly stated.
How to prepare for a job interview at CK Group- Science, Clinical and Technical
✨Know Your Technical Stuff
Make sure you brush up on your knowledge of HPLC and GC techniques, as well as GMP and data integrity requirements. Be prepared to discuss your hands-on experience with these instruments and any troubleshooting you've done in the past.
✨Familiarise Yourself with SOPs
Since you'll be working in a regulated environment, it's crucial to understand Standard Operating Procedures (SOPs). Be ready to explain how you've followed SOPs in previous roles and how you ensure compliance with cGMP requirements.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving skills, especially regarding laboratory discrepancies or investigations. Think of specific examples where you've identified root causes or implemented corrective actions in your previous work.
✨Show Enthusiasm for Continuous Improvement
Demonstrate your interest in contributing to departmental improvement projects. Discuss any past experiences where you've been involved in revising SOPs or improving laboratory methods, highlighting your proactive approach to quality control.
