QA Scientist Analyst

Proclinical Staffing; Lewes; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading recruitment agency in the United Kingdom is seeking a detail-oriented QA Scientist Analyst to ensure the quality and safety of pharmaceutical products. The successful candidate will conduct rigorous testing and collaborate with teams to resolve issues. Ideal candidates will have a strong background in Chemistry and an understanding of GMP and GLP principles. This contract role is situated in Southern England, focusing on maintaining high-quality standards in a fast-paced environment.

Qualifications

• Strong understanding of GMP and GLP principles.
• Excellent reporting skills with experience using SOPs.
• Methodical and detail-oriented approach.

Responsibilities

• Conduct routine testing of production and stability samples.
• Calibrate and maintain analytical equipment for accuracy.
• Investigate Out-of-Specification (OOS) results.

Skills

Attention to detail

Analytical techniques

Collaboration

Education

Background in Chemistry or related discipline (HNC or equivalent preferred)

Tools

HPLC

Job description

Overview

Proclinical is seeking a detail-oriented QA Scientist Analyst to join a dynamic and collaborative team on a contract basis. This role focuses on ensuring the quality and safety of pharmaceutical products through rigorous testing and adherence to industry standards. You will play a key part in maintaining compliance and supporting the release of high-quality products.

Please note: The ideal candidate is located in, or able to cover, the capital city and key areas across Southern England.

Responsibilities

• Conduct routine testing of production and stability samples, ensuring timely completion.
• Calibrate and maintain analytical equipment to ensure accuracy.
• Perform qualitative and quantitative analysis using techniques such as HPLC, Karl Fischer, and dissolution testing.
• Investigate Out-of-Specification (OOS) results and collaborate with relevant teams for resolution.
• Verify analytical data and testing performed by other analysts.
• Maintain high safety and Good Laboratory Practice (GLP) standards, ensuring training records are current.
• Validate equipment and methods as required.
• Communicate daily with analysts and team leaders regarding testing progress and results.
• Provide data and reports to internal stakeholders as needed.
• Lead small teams on specific analytical techniques, such as HPLC, when necessary.

Key Skills and Requirements

• Background in Chemistry or a related scientific discipline (HNC or equivalent preferred).
• Strong understanding of GMP and GLP principles.
• Excellent reporting and documentation skills, with experience using SOPs and site systems.
• Methodical and detail-oriented approach to work.
• Proficiency in computer systems and software.
• Effective communication and interpersonal skills.
• Adaptability to work in a fast-paced environment.
• Collaborative and team-oriented mindset.

If you are having difficulty in applying or if you have any questions, please contact Molly Colclough at [e-mail].

Apply Now:

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy