Scientist II or III AMS (material science/ analytical science)

ZipRecruiter; King's Lynn and West Norfolk; On-site; GBP 100,000 - 125,000; Full time

Job summary

A pharmaceutical testing laboratory is seeking a skilled analytical scientist to join their team in King's Lynn. The role involves performing analysis of various samples using advanced techniques, maintaining instruments, and preparing detailed reports. Candidates should have a PhD in a related field and relevant laboratory experience. This position offers an opportunity to work in a collaborative environment and contribute to critical projects.

Qualifications

• PhD or substantial practical work experience in a scientific field.
• Minimum of one year relevant pharmaceutical laboratory experience.
• Working knowledge of techniques such as HPLC/UPLC, laser diffraction, etc.

Responsibilities

• Perform routine and non-routine analysis of samples in a GMP environment.
• Maintain and troubleshoot analytical instruments.
• Prepare reports and present results professionally.

Skills

Analytical techniques knowledge

Attention to detail

Problem-solving

Education

PhD in a relevant scientific field

Tools

HPLC

Empower

OpenLAB

Job description

Overview

Job Description

Responsibilities

• Working in a multidisciplinary team in a GMP environment, performing routine and non-routine analysis of samples such as raw materials, excipients, APIs, drug products and other types of samples
• Preparing reagents and solutions for use in analysis
• Performing analytical testing of samples using chromatography and other wet chemistry techniques
• Development and validation of analytical methods that are appropriate for the requirements of the individual project, under supervision.
• Supporting the team by undertaking training and performing projects in physical properties and materials characterisation areas using techniques such as laser diffraction, PXRD, microscopy, thermal analysis etc.
• Following scientific methods, protocols, SOPs and Pharmacopoeia accurately and independently
• Providing high quality, right first-time, scientifically sound reports and CofAs to clients, meeting their deadlines
• Processing and interpreting data, performing calculations, drawing conclusions and reporting, highlighting aberrant or suspect results, and working with supervisor to investigate
• Presenting results verbally and in writing, both internally and externally, in a professional manner
• Maintenance and troubleshooting of analytical instruments, and solving challenging problems either independently or with assistance from senior personnel
• Performing experiments and documentation in accordance SOPs, data integrity and good documentation practices, and Good Manufacturing Practice (GMP) principles
• Raising and reporting any OOS and deviations, assisting with investigations and CAPAs, and contributing to laboratory audits as required
• Keeping up-to-date with any technological and methodological advancements to support future projects and increase lab capabilities
• Organising and managing multiple projects simultaneously if required, working in a flexible manner and able to switch priorities at short notice
• Sharing knowledge and expertise to foster a collaborative environment

Skills, Education & Qualifications

• PhD in a relevant scientific field (such as Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics), or substantial practical work experience
• A minimum of one year relevant experience of analysis in a pharmaceutical testing laboratory, or equivalent
• Working knowledge of a wide range of techniques such as HPLC/UPLC, laser diffraction, microscopy, thermal analysis, PXRD etc.
• A strong foundation of basic principles of chemistry and separation science is essential
• Experience in method development and validation is desirable but not required
• A strong understanding of the pharmaceutical development process and the industry would be advantageous
• Experience with Empower, OpenLAB, ChemStation or similar software
• Knowledge or experience of working within GxP regulations
• Excellent attention to detail and ability to spot inconsistencies