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Senior Analytical Development Scientist

Experience Dependent
Job Reference: J5636300
Updated On: 14/04/2022
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Contract Research Organisation, Contract Manufacturing Organisation

Skills: Chemistry - Analytical - HPLC (Method Development), Chemistry - Analytical - Method Development Only, Chemistry - Analytical - Development and Validation Analyst

Job Information

Role Overview

We are currently looking for an Senior Analytical Development Scientist to join a leading company based in the Nottinghamshire area. The Senior Scientist in the Analytical Development Laboratory you will become part of a team which supports the other sections of the Pharmaceutical Development services in the completion of development activities and/ or stability testing, as agreed in line with business needs.

Key Duties and Responsibilities

Your duties as the Senior Analytical Development Scientist will be varied however the key duties and responsibilities are as follows:

1. As the Senior Analytical Development Scientist you will analyse pharmaceutical samples, using analytical techniques including HPLC, LCMS and dissolution, to the required standards producing high quality data.

2. You will complete both development and stability testing, ensuring you meet all safety and current Good Manufacturing Practices (cGMP) requirements during day to day working. To be responsible for own housekeeping within the lab and ensure the lab is left in a suitable state for use by others.

3. As the Senior Analytical Development Scientist you will ensure that equipment/instrumentation is calibrated and maintained and that laboratory records/documentation complies with cGMPs.

4. You will complete method development and validation providing support to junior members of the team.

Role Requirements

To be successful in your application to this exciting opportunity as the Senior Analytical Development Scientist we are looking to identify the following on your profile and past history:

1. Relevant degree in Chemistry or related discipline.

2. Proven industry experience in laboratory environment working to GMP standards.

3. A working knowledge and practical experience with analytical techniques such as HPLC, LCMS and Dissolution testing oral solid dose. Experience in method development and method validation. Experience in supervising or line managing a team of analysts is desirable .

Key Words: HPLC, Dissolution, Analytical, Development, Method development, Method validation, GMP, Solid.
Edward McNulty
Your Recruitment ConsultantEdward
DisclaimerHyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.