QC Analytical Chemist: Chromatography & Spectroscopy

Pharmaron; Rushden; On-site; GBP 28,000 - 36,000; Full time

Benefits offered by this job

Collaborative culture

Job summary

Pharmaron is seeking an Analytical chemist to join the Rushden facility in the Chemistry Quality Control Department. The role involves performing QC analyses using chromatographic and spectroscopic techniques, generating data interpretations, and producing QA-compliant analytical reports.

You will maintain instruments, ensure adequate materials, and support method verification, validation, and documentation. A can-do attitude and collaboration with teams are essential.

Qualifications

• Degree in Chemistry or relevant experience.
• Good grounding in chromatographic and spectroscopic techniques.
• Strong communication skills, written and verbal.

Responsibilities

• Carry out QC analysis of materials from custom synthesis teams.
• Perform QC analysis of materials on stability.
• Interpret analytical results and explain them to a wider audience.
• Maintain accurate laboratory records.
• Maintain QC instruments and report faults.
• Participate in method verification/validation and controlled documents.
• Prepare out-of-specification and deviation documentation.
• Support validation/qualification of laboratory equipment.
• QC release raw materials from Quarantine for GMP manufacture.
• Carry out QC review of analytical data.

Skills

Chemistry degree

Chromatographic techniques

Spectroscopic techniques

Communication skills

Teamwork

Time management

Problem solving

Proactivity

Analytical experience

Data analysis

Spreadsheet skills

Regulatory knowledge

Education

Chemistry degree

Job description

Pharmaron is seeking an Analytical chemist to join the Rushden facility in the Chemistry Quality Control Department. The role involves performing QC analyses using chromatographic and spectroscopic techniques, generating data interpretations, and producing QA-compliant analytical reports.

You will maintain instruments, ensure adequate materials, and support method verification, validation, and documentation. A can-do attitude and collaboration with teams are essential.