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QC Validation Analyst

CambridgeshirePermanent
Experience Dependant
Job Reference: J5631763
Updated On: 16/07/2019
Status: Now Interviewing
Hyper Recruitment Solutions
Sectors: Pharmaceutical

Skills: Biochemistry - QC / Stability, Chemistry - Analytical - HPLC (Method Devlopment), Quality Assurance - Validation

Job Information

Role Overview

We are currently looking for a QC Validation Analyst to join a leading Pharmaceutical company based in the Cambridgeshire area on a 6 month contract basis. As the QC Validation Analyst you will be responsible for providing analytical support to a range of production processes and products.

Key Duties and Responsibilities

KEY DUTIES AND RESPONSIBILITIES:

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

1. You will be responsible for the performing a range of Analytical technique to support a range of Validation projects by performing a range of Analytical Testing of Pharmaceutical products using HPLC, Karl Fisher, Dissolution and Particle Size equipment.

2. To actively contribute to the progression of ongoing process validation projects by conducting all aspects of analytical testing using a variety of analytical techniques.

3. You will be responsible for utilising a range of software and information systems and maintaining accurate written records and reports in accordance with GMP/GLP requirements.

4. You will work effectively across a multi-disciplinary team as well as keeping attention to detail, strong organisational, effective interpersonal and communication skills.

Role Requirements

ROLE REQUIREMENTS:

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

1. Degree in Chemistry or relevant Scientific discipline

2. Proven industry experience in a Pharmaceutical GMP environment and with a range of analytical techniques including HPLC, Karl Fisher, Particle Size and Dissolution.

3. A working knowledge and practical experience with Wet Chemistry and understanding of ICH guidelines


Key Words: Validation / QC / Quality Control / Analyst / Pharmaceutical / Chemistry / Analytical Equipment / HPLC / Karl Fisher / Dissolution / Particle Size / GMP / Production / Process Improvement / ICH / Regulatory / Compliance / New Material / Process Validation

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties 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 professionals and scientists. We look forward to helping you with your next career moves.
Aliyah Iheanacho
Your Recruitment ConsultantAliyah IheanachoAliyah.Iheanacho@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.