QA Scientist

ZipRecruiter; Worthing; On-site; Full time

Job summary

An established industry player in pharmaceuticals is seeking a QA Scientist Analyst to join their team in Worthing. This exciting role involves conducting critical testing of production and stability samples, ensuring compliance with safety and quality standards. You will utilize a range of analytical techniques, including HPLC, to deliver accurate results and support OOS investigations. Join a collaborative environment where your expertise will directly impact the quality of pharmaceutical products. If you are passionate about quality assurance and have a keen eye for detail, this opportunity is perfect for you.

Qualifications

• Experience in quality assurance and analytical testing in pharmaceuticals.
• Strong knowledge of HPLC and other analytical techniques.

Responsibilities

• Test production and stability samples, ensuring timely results.
• Calibrate and maintain analytical equipment, adhering to GLP standards.

Skills

Analytical Techniques

HPLC

Quality Control

Data Verification

GLP Compliance

Education

Degree in Chemistry or related field

Tools

Karl Fischer

Analytical Equipment

Job description

Job Description

Job Title: QA Scientist Analyst

Job Length: 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.

Key Responsibilities:

1. 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. Conduct OOS investigations and discuss the outcome with Team Leader, or relevant production Department, QA manager or a Qualified Person, as required.
5. Check and verify analytical testing and data generated by other analysts.
6. 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. Supply data/reports to Value Stream as requested.
10. Communicate with the relevant Value Stream to progress OOS investigations.