Design Control Officer
Hyper Recruitment Solutions are currently looking for a Design Control Officer to join a leading Pharmaceutical company based in Northern Ireland. As ... View Job
QA/Compliance Officer (Manufacturing)
Hyper Recruitment Solutions are currently looking for a QA/Compliance Officer (Manufacturing) to join a leading Bio-Pharmaceutical company based in th... View Job
Hyper Recruitment Solutions are currently looking for a GMDP Quality Auditor to join a leading Global Pharmaceutical company based in the Cambridgeshi... View Job
Hyper Recruitment Solutions are currently looking for a QA Auditor to join a leading pharmaceutical services company based in the Manchester area. As the QA Auditor you will be responsible for performing audits/ checks for GLP, GMP, GCP and non-GxP data as necessary to assure data integrity.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QA Auditor will be varied however the key duties and responsibilities are as follows:
1.Perform GLP, GMP, GCP and related quality system audits necessary to assure compliance with all relevant current National and International Quality Standards and customer requirements.
2.Assist the Quality Assurance Senior Team Leader in the overall implementation of the Quality function.
3.Check/ audit analytical technical data, associated records, facility and operational systems, to monitor and assure management of data integrity/ compliance with all relevant regulatory requirements.
4.Provide general support to all Quality Unit activities relating to GLP, GMP, GCP, and other similar Quality Systems established in order to ensure that the appropriate standards are maintained and where necessary, improved.
To be successful in your application to this exciting opportunity as the QA Auditor we are looking to identify the following on your profile and past history:
1. Ideally a relevant degree in a BioChemistry or Chemistry (or related scientific discipline).
2. Proven industry experience of performing detailed audits for data integrity within the regulatory framework.
3. A working knowledge and practical experience with GLP, GMP, GCP and other analytical related quality standards. Industry experience in analytical science (chromatographic methods e.g. HPLC, GC, LC etc. and/ or other pharmaceutical characterisation techniques).
Hyper 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.