QC Analytical Chemist

Agilent Technologies LDA UK Limited; Church Stretton; On-site; GBP 28,000 - 42,000; Full time

Benefits offered by this job

Company pension scheme

Private health care

Career development opportunities

Work-Life-Balance programs

Job summary

Agilent Technologies LDA UK Limited in Church Stretton is seeking a QC Analytical Chemist to join our Quality Control team and ensure materials meet stringent specifications.

You will perform routine and non-routine analyses, contribute to method development, and support cross-functional projects across Manufacturing, R&D, and Quality teams.

Qualifications

• Bachelor's or Master's in Chemistry or closely related discipline.
• Hands-on practical experience in a Quality Control or analytical testing laboratory.
• Strong proficiency with HPLC / GPC equipment and data analysis.

Responsibilities

• Perform chemical and physical testing of materials according to SOPs.
• Develop and validate test methods; support method optimization and investigations.
• Document, review, and ensure data integrity and regulatory compliance.

Skills

Analytical Chemistry

Quality Control

Data Analysis

SOPs

Education

Bachelor's degree in Chemistry

Master's degree in Analytical Chemistry

Tools

HPLC

GPC

GC-MS

LC-MS

FTIR

UV-Vis

ICP-OES

ICP-MS

Titration

Job description

Job DescriptionAt Agilent, we inspire and support discoveries that advance the quality of life. We provide life science, diagnostic, and applied market laboratories worldwide with instruments, services, consumables, applications, and expertise. Our mission is to enable customers to gain the insights they seek – so they can do what they do best: improve the world around us. Learn more about us at www.agilent.comAre you an experienced Analytical Chemist with a passion for quality, precision, and problem-solving? We are looking for a QC Analytical Chemist to join our fast-paced Quality Control team based at our Church Stretton manufacturing site.We design and manufacture highly specialised polymeric particles for diagnostics, solid-phase synthesis, and chromatographic applications supporting a wide range of industries.In this role, you will play a critical part in ensuring our raw materials, intermediates, and finished products meet stringent quality and performance specifications. Working with cutting-edge analytical instrumentation you will conduct both routine and complex testing, contribute to method development, and help drive process improvements within the lab.If you thrive in an environment of technical independence, continuous improvement, and collaborative innovation, we want to hear from you.Key ResponsibilitiesTesting & Analytical OperationsRoutine & Non-Routine Analysis: Conduct chemical and physical property testing of raw materials, intermediates, and finished products according to Standard Operating Procedures (SOPs).Test Method Development: Execute validation, assays and MSA studies to support product lifecycle and quality standards.Quality, Compliance & Documentation.Data Integrity & Review: Compile, document and review test data for strict compliance with specifications. Report any abnormalities, out-of-specification (OOS) results, or process deviations.Product Release: Certification, stock control and authorize release of conforming materials.SOP Maintenance: Author, revise, and update Standard Operating Procedures as needed to align with continuous improvement and regulatory standards.Projects & Cross-Functional CollaborationSpecial & Cross-Functional Projects: Lead and contribute to analytical projects focused on method optimization, new test introduction, and technical investigations alongside Manufacturing, R&D, Engineering and Quality teams.Technical Support: Provide analytical expertise for customer investigations and cross-functional business initiatives.Knowledge Sharing: Support team training and share technical knowledge across the laboratory where appropriate.QualificationsQualifications & RequirementsEducation: Bachelor's or Master's degree in Chemistry, Analytical Chemistry, or a closely related scientific discipline.Experience: Hands-on practical experience working in a Quality Control or analytical testing laboratory environment.Analytical Techniques: Strong proficiency with HPLC / GPC equipment, method application, and general analytical data analysis.Chromatography & Instrumentation (Desirable): While GC-MS or LC-MS skills are highly desirable to support occasional specialized testing, the role is primarily focused on general liquid chromatography and wet chemistry. Additional experience with FTIR, UV-Vis, ICP-OES/ICP-MS, or automated titration is a plus.What We Offer:Outstanding company culture and working environment.Career development opportunities.Competitive compensation and benefits package.Work-Life-Balance programs.Company pension scheme.Private health care.A position within an international organization, offering a multifaceted working environment with exciting challenges and opportunities.Additional DetailsThis job has a full time weekly schedule.Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.Travel Required:NoShift:DayDuration:No End DateJob Function:Quality/Regulatory