MeiraGTx Jobs in United Kingdom

Provide subject matter expertise in the establishment improvement troubleshooting and execution of maintenance and calibration activities to ensure that assets required for the GMP manufacture and testing of gene therapy products are available and fit for use in line with busines ...

To assist the Tech Transfer department in collection and analysis of data from Tech Transfer and manufacturing processes. Creation and maintenance of appropriate data storage and analytical systems. Identification of key data in MeiraGTx documentation. · ...

To assist the Tech Transfer department in collection and analysis of data from Tech Transfer and manufacturing processes.Contribute to general Tech Transfer activities. · ...

Overview · The primary purpose of the Clinical Trials Administrator (CTA) is to administer, maintain and co-ordinate the logistical aspects of clinical trials in compliance with Good Clinical Practice (GCP) and relevant Standard Operating Procedures (SOPs). They also act as a piv ...

A leading biopharmaceutical firm in Greater London seeks a Clinical Trials Administrator (CTA) to coordinate the logistical aspects of clinical trials while ensuring adherence to Good Clinical Practice (GCP). Responsibilities include managing study documents, assisting in regulat ...

The primary purpose of the Clinical Trials Administrator (CTA) is to administer, maintain and co-ordinate the logistical aspects of clinical trials in compliance with Good Clinical Practice (GCP) and relevant Standard Operating Procedures (SOPs). They also act as a pivotal point ...

To assist the Tech Transfer department in collection and analysis of data from Tech Transfer and manufacturing processes. · ...

To assist the Tech Transfer department in collection and analysis of data from Tech Transfer and manufacturing processes. · Educated to degree level, with industrial experience preferred in pharmaceuticals, biotechnology or scientific manufacture. · ...

The Clinical Trials Administrator is responsible for administering and co-ordinating the logistical aspects of clinical trials in compliance with Good Clinical Practice (GCP) and relevant Standard Operating Procedures (SOPs). They act as a pivotal point of contact & support for t ...

The primary purpose of the Clinical Trials Administrator (CTA) is to administer,maintain and co-ordinate the logistical aspects of clinical trials in compliance with Good Clinical Practice (GCP) and relevant Standard Operating Procedures (SOPs). They also act as a pivotal point o ...

The primary purpose of the Clinical Trials Administrator (CTA) is to administer, maintain and co-ordinate the logistical aspects of clinical trials in compliance with Good Clinical Practice (GCP) and relevant Standard Operating Procedures (SOPs). They also act as a pivotal point ...

OverviewThe primary purpose of the Clinical Trials Administrator (CTA) is to administer, maintain and co-ordinate the logistical aspects of clinical trials in compliance with Good Clinical Practice (GCP) and relevant Standard Operating Procedures (SOPs). They also act as a pivota ...

The Clinical Trials Administrator will administer, maintain and co-ordinate the logistical aspects of clinical trials in compliance with Good Clinical Practice · Arranging & participating in the organisation of Investigator Meetings & Study Team Meetings. · Assist with the Ethic ...

The Senior QC Analytical Scientist is responsible for the testing of gene therapy products and associated materials used for manufacturing to EU and FDA GMP requirements. · ...

To assist the Tech Transfer department in collection and analysis of data from Tech Transfer and manufacturing processes. Assist in putting in place systems of work for collation and creation of data sets from Tech Transfer and manufacturing processes. Contribute to general Tech ...

The job involves providing ongoing engineering validation support to MeiraGTx sites, ensuring compliance with EU and FDA regulations. The successful candidate will have a degree in Human Health or Sciences and at least 5 years of experience in Engineering Validation department. T ...

A leading biopharmaceutical firm in Greater London seeks a Clinical Trials Administrator (CTA) to coordinate the logistical aspects of clinical trials while ensuring adherence to Good Clinical Practice (GCP). Responsibilities include managing study documents, assisting in regulat ...

The primary purpose of the Clinical Trials Administrator (CTA) is to administer, maintain and co-ordinate the logistical aspects of clinical trials in compliance with Good Clinical Practice (GCP) and relevant Standard Operating Procedures (SOPs) · ...