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QA Scientist Analyst - GSK0JP00106075

SRG

Worthing

On-site

Full time

7 days ago
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Job summary

An established industry player in pharmaceuticals is seeking a QA Scientist Analyst for a 6-month contract. This role involves testing production and stability samples, calibrating analytical equipment, and conducting qualitative and quantitative analyses using advanced techniques like HPLC. The successful candidate will ensure compliance with GLP and safety standards while collaborating with a team of analysts. If you are passionate about quality assurance in a dynamic environment and ready to make an impact, this opportunity is perfect for you.

Qualifications

  • Experience in testing production and stability samples in a pharmaceutical environment.
  • Ability to perform OOS investigations and maintain safety standards.

Responsibilities

  • Test routine production and stability samples to meet lead-time targets.
  • Calibrate and maintain analytical equipment and perform validations.

Skills

Qualitative and Quantitative Analysis
Analytical Techniques
HPLC
Calibration
GLP Compliance

Tools

Karl Fischer
Analytical Equipment

Job description

Job Title: QA Scientist Analyst

Job Type: 6 Month Contract

Employment Start Date: ASAP

Onsite requirement: 5 days per week on site

Industry: Pharmaceuticals

Location: Worthing, England

Salary: £15.64 per hour - PAYE

SRG are working with a global leader in the pharmaceutical industry to find a new QA Scientist Analyst for their site in Worthing.

Responsibilities:
  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 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.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

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