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Analytical Method Validation Analyst

West YorkshirePermanent
Experience Dependent
Job Reference: J5635530
Updated On: 13/10/2021
Status: Now Interviewing
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Contract Manufacturing Organisation, Contract Testing Organisation, Life Sciences, Science

Skills: Chemistry - Analytical - HPLC (Method Development), Chemistry - Analytical - GCMS, Chemistry - Analytical - LCMS, Chemistry - Development, Chemistry - Analytical - Team Leader / Supervisor (5 staff max), Chemistry - PhD Analytical, Chemistry - Analytical - Method Validation Only, Chemistry - Analytical - Method Development Only, Chemistry - Analytical - Development and Validation Analyst, Chemistry - Analytical - UPLC

Job Information

Role Overview

Are you an experienced Analytical Method Validation Analyst looking for a new exciting job opportunity?

We are currently looking for Analytical Method Validation Analysts as well as a Senior Analyst to join a leading pharmaceutical company based in the West Yorkshire area on a 23 month fixed term contract.

As the Analytical Method Validation Analyst you will be responsible for developing and validating analytical methods to support the analytical life cycle management program.

The Senior Analytical Method Validation Analyst will have the additional responsibility of providing analytical support in performing gap analysis and risk assessing legacy analytical methods to support the life cycle management approach.

Key Duties and Responsibilities

Your duties as the Analytical Method Validation Analyst will be varied however the key duties and responsibilities are as follows:

1. To develop, validate and transfer analytical methods (including dissolution methodology) that will adequately determine the necessary product characteristics that will be required to release drug product and to monitor the storage stability of legacy products (without supervision for the Senior Analyst level).

2. You will be responsible for reviewing method validation supporting existing analytical methods and identify gaps against ICH and other regulatory requirements.

3. You also be required to produce and/or review validation protocols and reports, methods of analysis, COSHH assessments, SOP / WRK instructions, and relevant scientific protocols and other reports in a format that can be utilized by other departments, providing relevant feedback on the content and style of documentation to ensure compliance with company and regulatory requirements.

4. Both levels of method validation analysts will participate in cross functional teams at project-related meetings, lead or facilitate technical discussions and will maintain interdepartmental relationships and positively promote the department and its objectives.

Role Requirements

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

1. Degree in a pharmaceutical science / chemistry degree.

2. To be considered for either levels, you must have proven experience in a variety of analytical instruments and software utilised for physical and chemical analysis - most importantly, you must have strong HPLC experience including analytical method validation.

3. Experience working in a pharmaceutical GMP environment is also essential.
Debra Fong
Your Recruitment ConsultantDebra Fongdebra.fong@hyperec.com
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.