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- Tasks: Conduct QC testing of raw materials in a pharma lab using chemical analysis and instrumentation.
- Company: Join a leading multi-Pharma client based in Speke, Liverpool.
- Benefits: Enjoy a competitive hourly rate of £13.00-£14.00 and a 12-month contract.
- Why this job: Gain hands-on experience in a dynamic environment while contributing to healthcare innovation.
- Qualifications: Minimum 2 years in a QC lab with experience in classical chemical analysis and instrumentation.
- Other info: Candidates must have the right to work in the UK; no visa sponsorship available.
PE Global is currently recruiting for a Raw Materials QC Analyst for a leading multi-Pharma client based in Speke, Liverpool. This is an initial 12 month contract position paying £13.00-£14.00 per hour PAYE.
Duties of the role/Responsibilities:
- QC testing of raw materials in a pharma lab.
- Using classic chemical analysis (e.g. titrations, moisture determination, chemical IDs etc.) and instrumentation (NIR, mid-IR etc).
- Follow compendial procedures (e.g. USP and Ph.Eur).
Education/Experience:
- Ideally min 2 years experience in a QCL raw materials testing lab.
- Experience with classical chemical analysis (e.g. titrations, moisture determination, chemical IDs etc.) and instrumentation (NIR, mid-IR etc).
- Familiar with following compendial procedures (e.g. USP and Ph.Eur).
- Experience with cGMP would be ideal but not essential.
Interested candidates should submit an updated CV.
Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK.
Raw Materials QC Analyst employer: ZipRecruiter
Contact Detail:
ZipRecruiter Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Raw Materials QC Analyst
✨Tip Number 1
Familiarise yourself with the specific compendial procedures mentioned in the job description, such as USP and Ph.Eur. This knowledge will not only help you during the interview but also demonstrate your commitment to quality control standards.
✨Tip Number 2
Brush up on your classical chemical analysis techniques, especially titrations and moisture determination. Being able to discuss these methods confidently can set you apart from other candidates.
✨Tip Number 3
If you have experience with instrumentation like NIR or mid-IR, be prepared to share specific examples of how you've used these tools in previous roles. Real-world applications can make a strong impression.
✨Tip Number 4
Network with professionals in the pharmaceutical industry, particularly those who work in quality control. They may provide insights or even referrals that could enhance your chances of landing the job.
We think you need these skills to ace Raw Materials QC Analyst
Some tips for your application 🫡
Understand the Role: Read the job description carefully to understand the specific responsibilities and requirements for the Raw Materials QC Analyst position. Highlight your relevant experience in QC testing and classical chemical analysis.
Tailor Your CV: Make sure your CV is tailored to the job. Emphasise your experience with raw materials testing, classical chemical analysis techniques, and any familiarity with compendial procedures like USP and Ph.Eur.
Highlight Relevant Skills: In your application, clearly outline your skills related to QC testing, including any experience with instrumentation such as NIR and mid-IR. Mention your understanding of cGMP if applicable.
Proofread Your Application: Before submitting, proofread your CV and any accompanying documents to ensure there are no errors. A well-presented application reflects your attention to detail, which is crucial in a QC role.
How to prepare for a job interview at ZipRecruiter
✨Brush Up on Your Technical Skills
Make sure you're well-versed in classic chemical analysis techniques like titrations and moisture determination. Be prepared to discuss your hands-on experience with instrumentation such as NIR and mid-IR, as these will likely come up during the interview.
✨Know the Compendial Procedures
Familiarise yourself with compendial procedures like USP and Ph.Eur. Being able to demonstrate your understanding of these standards will show that you are serious about quality control in the pharmaceutical industry.
✨Highlight Relevant Experience
With a minimum of 2 years' experience in a QC lab being ideal, be ready to share specific examples from your past roles. Discuss any relevant projects or challenges you've faced and how you overcame them.
✨Understand cGMP Principles
While experience with cGMP is not essential, having a basic understanding of Good Manufacturing Practices will set you apart. Be prepared to discuss how these principles apply to raw materials testing and quality assurance.
