Quality Compliance Officer - Pharma
RHL has a long-standing relationship with leading UK based biopharma manufacturing company, which focus on unique life-saving vaccination products. Based on ongoing expansion they are recruiting for a Quality Compliance Officer to join their rapidly growing, stable team.
Since being established in 2015, the company have doubled in size and are now looking for someone with significant experience in a GMP regulated environment. They are riding a wave of success based on their completely innovative vaccines which are in high demand, and are looking to move forward to the next phase of the companies development. Y
You will manage the non-conformance and CAPA systems to support the manufacturing and testing of pharmaceutical products to GMP, as well as change control and risk management systems and internal and supplier audit management programmes. You are also responsible for the product review process the management of QA environmental compliance and the provision of QA oversight of manufacturing and testing activities.
The role will for Quality Compliance Officer requires you -
To support the co-ordination and planning of the IPT workload, ensuring Quality matters are considered and acted upon in a compliant fashion.
To actively participate in Quality investigations, change controls and risk assessments associated with the IPT to ensure Quality considerations are taken into account.
To facilitate and lead structured investigations using recognised models such as "5Whys" and "FMEA".
To perform the review and approval of a number of key documents associated to the IPT including but not limited to: validation, SOPs, change controls, investigations, risk assessments, pre manufacturing checks, facility release.
To perform review of batch manufacturing records and release relevant material for the next stage of manufacture.
To provide appropriate QA oversight of manufacturing and testing processes within the IPT to support the business (including occasional out of hours).
To participate in the data gathering/review for the quarterly trending reports and annual PQR for the related stage of manufacture.
If you feel you have the experience please apply with your CV for more information - you will have been educated to degree level or HND (e.g. Microbiology, or a related subject) level, Experience in operating quality systems in a GMP environment, as well as the right to work in the UK.
Please apply to Kosh Santra below
Since being established in 2015, the company have doubled in size and are now looking for someone with significant experience in a GMP regulated environment. They are riding a wave of success based on their completely innovative vaccines which are in high demand, and are looking to move forward to the next phase of the companies development. Y
You will manage the non-conformance and CAPA systems to support the manufacturing and testing of pharmaceutical products to GMP, as well as change control and risk management systems and internal and supplier audit management programmes. You are also responsible for the product review process the management of QA environmental compliance and the provision of QA oversight of manufacturing and testing activities.
The role will for Quality Compliance Officer requires you -
To support the co-ordination and planning of the IPT workload, ensuring Quality matters are considered and acted upon in a compliant fashion.
To actively participate in Quality investigations, change controls and risk assessments associated with the IPT to ensure Quality considerations are taken into account.
To facilitate and lead structured investigations using recognised models such as "5Whys" and "FMEA".
To perform the review and approval of a number of key documents associated to the IPT including but not limited to: validation, SOPs, change controls, investigations, risk assessments, pre manufacturing checks, facility release.
To perform review of batch manufacturing records and release relevant material for the next stage of manufacture.
To provide appropriate QA oversight of manufacturing and testing processes within the IPT to support the business (including occasional out of hours).
To participate in the data gathering/review for the quarterly trending reports and annual PQR for the related stage of manufacture.
If you feel you have the experience please apply with your CV for more information - you will have been educated to degree level or HND (e.g. Microbiology, or a related subject) level, Experience in operating quality systems in a GMP environment, as well as the right to work in the UK.
Please apply to Kosh Santra below