At a Glance
- Tasks: Conduct testing on raw materials and finished products in a lab setting.
- Company: Join a leading global pharmaceutical manufacturer focused on innovative vaccine technologies.
- Benefits: Enjoy a competitive rate of £15.25 p/h with a flexible 4 on, 4 off shift pattern.
- Other info: Contract runs until the end of December, perfect for students seeking temporary work.
- Why this job: Be part of a team making a real impact in public health through vaccine development.
- Qualifications: Degree in Chemistry, Biochemistry, or Biomedical Science; prior GMP experience preferred.
QC Analyst (Temporary) Skipton, UK (On-site) Temporary 3 Month SRG are recruiting for a number of QC Analysts to support a busy GMP Manufacturing site in North Yorkshire. This will be a temporary position for an initial period of 3 Month with the potential to be extended. This is an urgent position and can start as soon as 1st of September. As part of the QC team, you will play a crucial part in carrying out Quality testing on raw materials, semi-finished goods, packaging materials, and medicinal products, all within a GMP environment. Key Responsibilities Performing analytical and physical tests including HPLC, UV-VIS, DLC, MID-IR, (auto) titration, water determination Karl Fischer, TOC, etc. Releasing of raw materials, semi-finished products and packaging materials for use in production Performing analysis for process, product, cleaning and equipment validation studies Conducting analysis for stability studies
Quality Control Analyst employer: SRG
SRG in Scotland is an excellent employer, offering a dynamic work culture that fosters innovation and collaboration among its development team. With a strong focus on employee growth, you will have access to continuous learning opportunities and the chance to work on impactful projects in a thriving contract manufacturing environment. The company's commitment to safety and high standards ensures that you can take pride in your contributions while enjoying a supportive and engaging workplace.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Control Analyst
✨Tip Number 1
Familiarise yourself with the specific testing methods used in the pharmaceutical industry, especially those related to analytical and bioassay techniques. This knowledge will not only help you during interviews but also demonstrate your genuine interest in the role.
✨Tip Number 2
Network with professionals in the pharmaceutical field, particularly those who work in quality control or similar roles. Attend industry events or join relevant online forums to gain insights and potentially get referrals that could boost your application.
✨Tip Number 3
Brush up on your understanding of GMP (Good Manufacturing Practice) regulations, as this is crucial for a QC Analyst role. Being able to discuss how you would ensure compliance in your work can set you apart from other candidates.
✨Tip Number 4
Prepare to discuss your previous laboratory experiences in detail, focusing on any troubleshooting you've done with assays. Highlighting your problem-solving skills will show that you're capable of handling the challenges that come with the role.
We think you need these skills to ace Quality Control Analyst
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights relevant experience in quality control and any specific skills related to analytical, molecular, and bioassay testing. Emphasise your degree in Chemistry, Biochemistry, or Biomedical Science.
Craft a Strong Cover Letter:Write a cover letter that connects your background to the job description. Mention your practical experience in a GMP regulated environment and how it aligns with the responsibilities of the QC Analyst role.
Highlight Communication Skills:Since strong verbal and written communication skills are essential for this role, provide examples in your application that demonstrate your ability to communicate effectively in a laboratory setting.
Review and Edit:Before submitting your application, review all documents for clarity and accuracy. Ensure there are no spelling or grammatical errors, as attention to detail is crucial in quality control.
How to prepare for a job interview at SRG
✨Know Your Science
Make sure you brush up on your knowledge of Chemistry, Biochemistry, and Biomedical Science. Be prepared to discuss specific testing methods and how they apply to the role of a QC Analyst.
✨Familiarise Yourself with GMP Standards
Since prior experience in a GMP regulated environment is desirable, it’s crucial to understand Good Manufacturing Practices. Be ready to explain how you’ve adhered to these standards in past roles.
✨Demonstrate Your Communication Skills
Strong verbal and written communication skills are essential for this position. Prepare examples of how you've effectively communicated complex scientific information in previous roles.
✨Prepare for Technical Questions
Expect to face technical questions related to analytical, biosafety, and cell science testing. Review common assays and troubleshooting techniques to showcase your problem-solving abilities during the interview.
