QA Scientist

JR United Kingdom; Worthing; On-site; Full time

Job summary

An established industry player in the pharmaceutical sector is seeking a meticulous QA Scientist Analyst to join their dynamic team in Worthing. In this pivotal role, you will be responsible for testing production and stability samples, calibrating equipment, and conducting in-depth analyses using advanced techniques such as HPLC. You will collaborate closely with a dedicated team, ensuring compliance with GLP standards and maintaining the highest safety levels. This is an exciting opportunity to contribute to critical quality assurance processes within a global leader, where your expertise will directly impact product quality and safety.

Qualifications

• Experience in analytical testing and quality assurance in a laboratory setting.
• Strong knowledge of GLP and safety standards.

Responsibilities

• Test production and stability samples to meet lead-time targets.
• Calibrate analytical equipment and perform validations as required.
• Conduct OOS investigations and maintain safety standards.

Skills

Qualitative and Quantitative Analysis

Analytical Techniques

HPLC

GLP Compliance

Calibration of Equipment

Education

Degree in Chemistry or related field

Tools

Karl Fischer

Dissolution Testing Equipment

Job description

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Onsite requirement: 5 days per week on site

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 Department, 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.