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QC Scientific Officer - Vaccine Production

WiltshirePermanent
Experience Dependent
Job Reference: J5634338
Updated On: 20/01/2021
Status: Now Interviewing
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Biotechnology, Life Sciences

Skills: Biochemistry - QC / Stability, Chemistry - Analytical - HPLC (routine), Life Sciences - Genomics

Job Information

Role Overview

We are currently looking for a QC Scientific Officer - Vaccine Production to join a leading Pharmaceutical company based in the Wiltshire area. As the QC Scientific Officer - Vaccine Production you will be responsible for the performing routine laboratory procedures, transfer of methodology and project work within the department at a local and international level. This is an exciting opportunity to join a new team within a sizeable QC function, performing testing to support the COVID-19 vaccine production.

Key Duties and Responsibilities

Your duties as the QC Scientific Officer - Vaccine Production will be varied however the key duties and responsibilities are as follows:

1. You will perform quality control analytical testing under cGMP conditions. You will also perform stability and in-process testing for product throughout life cycle.

2. As the QC Scientific Officer you will be required to prepare technical documentation including but not limited to analytical write-ups, SOPs, specifications, investigations and reports.

3. You will perform planned preventative maintenance and performance calibrations on equipment.

4. A responsibility of the QC Scientific Officer will include assisting in the transfer/validation of laboratory procedures and participating in continuous improvement activities.

Role Requirements

To be successful in your application to this exciting opportunity as the QC Scientific Officer - Vaccine Production we are looking to identify the following on your profile and past history:

1. Relevant degree in a Life Sciences related discipline plus industry experience.

2. Proven industry experience using analytical techniques including HPLC, pH, Ribogreen RNA assay and osmometry.

3. A working knowledge and practical experience in using activity and potency methods as well as method transfer or validation of activity./binding.


Key Words: QC / Quality Control / Scientific / Vaccine / Production / Manufacturing / GMP / cGMP / Good Manufacturing Practice / Biology / Life Sciences / Potency / Method Transfer / Validation / Activity / Binding / Analytical / HPLC / pH / Ribogreen / RNA / Assay / Osmometry / COVID-19 / COVID / SOPs / Investigations
Rachel Benjamin
Your Recruitment ConsultantRachel BenjaminRachel.Benjamin@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.