This job is closed and no longer accepting applications.
A new role as a Pharmaceutical Technology Officer is now available, your responsibilities will include:
Executing analytical validation and/or transfer activities to ensure the successful transfer and maintenance of all analytical procedures in accordance with company and GMP standards.
Supporting the Pharmaceutical Technology Specialist in the evaluation, planning, review and reporting of analytical validation and/or transfer activities to ensure the successful transfer and maintenance of all analytical procedures in accordance with company and GMP standards.
Assisting in issuing and checking of Analytical Methodology, Analytical Specifications, Submission, Process Optimisation, Validation and Cleaning Validation documents, in accordance with company and GMP standards.
Carrying out sampling, analysis of samples, and documentation of the analytical procedures performed according to cGLP and standards.
Ensuring GMP compliance as per local and EU procedures
Reviewing of documentation performed before sign-off.
Compiling reports, SOP’s test methods, and/or worksheets as required
A new role as a Pharmaceutical Technology Officer is now available, your responsibilities will include:
Executing analytical validation and/or transfer activities to ensure the successful transfer and maintenance of all analytical procedures in accordance with company and GMP standards.
Supporting the Pharmaceutical Technology Specialist in the evaluation, planning, review and reporting of analytical validation and/or transfer activities to ensure the successful transfer and maintenance of all analytical procedures in accordance with company and GMP standards.
Assisting in issuing and checking of Analytical Methodology, Analytical Specifications, Submission, Process Optimisation, Validation and Cleaning Validation documents, in accordance with company and GMP standards.
Carrying out sampling, analysis of samples, and documentation of the analytical procedures performed according to cGLP and standards.
Ensuring GMP compliance as per local and EU procedures
Reviewing of documentation performed before sign-off.
Compiling reports, SOP’s test methods, and/or worksheets as required