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QA Scientist - Analytical Technique

JR United Kingdom

Worthing

On-site

GBP 30,000 - 50,000

Full time

2 days ago
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Job summary

An established industry player is seeking a skilled QA Scientist to join their team in Worthing. This role involves testing production and stability samples, calibrating analytical equipment, and performing qualitative and quantitative analyses using advanced techniques like HPLC. You will play a crucial role in ensuring the highest safety and GLP standards while collaborating with a dedicated team. If you are passionate about quality assurance and ready to make a significant impact in a dynamic environment, this opportunity is perfect for you!

Qualifications

  • Experience in testing production and stability samples.
  • Proficient in calibrating and maintaining analytical equipment.

Responsibilities

  • Test routine production and stability samples to meet lead-time targets.
  • Perform qualitative and quantitative analysis of various compounds.

Skills

Analytical Techniques
HPLC
Qualitative Analysis
Quantitative Analysis
GLP Compliance

Education

Degree in Chemistry or related field

Tools

Analytical Equipment
Karl Fischer

Job description

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QA Scientist - Analytical Technique, Worthing, West Sussex
Client:

LanceSoft, Inc.

Location:

Worthing, West Sussex, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

5

Posted:

18.04.2025

Expiry Date:

02.06.2025

Job Description:

Title: QA Scientist Analyst

Duration: 6 months with possible extension

Location: Worthing, UK

Description:

  1. To test routine production and stability samples supplied from the site Value Streams and meet testing lead-time targets.
  2. Calibrate and maintain analytical equipment.
  3. Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (e.g., HPLC, Karl Fischer, dissolutions, etc.).
  4. To carry out OOS investigations and discuss the outcome with the Team Leader, or relevant production Dept, QA manager, or a Qualified Person, as required.
  5. To check and verify analytical testing and data generated by other analysts.
  6. To adhere to and help maintain the highest levels of safety and GLP within the section and ensure training records are kept up to date.
  7. Perform validation of equipment and methods as required.
  8. Daily liaison with both other analysts and team leader regarding testing and test results. May be required to take a lead role within a small team of analysts working together on a common analytical technique, e.g., HPLC.
  9. Supplying data/reports to Value Stream as requested.
  10. May be required to communicate with the relevant Value Stream to progress OOS investigations.
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