18/06/2024 | Fulltime | Berkeley | MundipharmaManagement of nonconformances and resolution of issues with key stakeholders and/or the Qualified Person as appropriate. - Input into the User Requirements Specification (URS) and co-oversight of Factory and Site Acceptance Testing (FAT/SAT). - Coordination of the execution of Installation Qualification (IQ
Save for later18/06/2024 | Fulltime | Cinderford | MundipharmaOf the validation strategy following a risk-based approach as per ICH Q9 and ensuring regulatory and GMP requirements are met. - Prepare validations protocols in line with defined and approved validation strategy and company templates. - Management of nonconformances and resolution of issues with key stakeholders
Save for later18/06/2024 | Fulltime | Drybrook | MundipharmaManagement of nonconformances and resolution of issues with key stakeholders and/or the Qualified Person as appropriate. - Input into the User Requirements Specification (URS) and co-oversight of Factory and Site Acceptance Testing (FAT/SAT). - Coordination of the execution of Installation Qualification (IQ
Save for later18/06/2024 | Fulltime | Stroud | MundipharmaOf the validation strategy following a risk-based approach as per ICH Q9 and ensuring regulatory and GMP requirements are met. - Prepare validations protocols in line with defined and approved validation strategy and company templates. - Management of nonconformances and resolution of issues with key stakeholders
Save for later18/06/2024 | Fulltime | Chalford | MundipharmaOf the validation strategy following a risk-based approach as per ICH Q9 and ensuring regulatory and GMP requirements are met. - Prepare validations protocols in line with defined and approved validation strategy and company templates. - Management of nonconformances and resolution of issues with key stakeholders
Save for later18/06/2024 | Fulltime | Berkeley | MundipharmaOf the validation strategy following a risk-based approach as per ICH Q9 and ensuring regulatory and GMP requirements are met. - Prepare validations protocols in line with defined and approved validation strategy and company templates. - Management of nonconformances and resolution of issues with key stakeholders
Save for later18/06/2024 | Fulltime | Wotton-under-Edge | MundipharmaOf the validation strategy following a risk-based approach as per ICH Q9 and ensuring regulatory and GMP requirements are met. - Prepare validations protocols in line with defined and approved validation strategy and company templates. - Management of nonconformances and resolution of issues with key stakeholders
Save for later18/06/2024 | Fulltime | Dursley | MundipharmaManagement of nonconformances and resolution of issues with key stakeholders and/or the Qualified Person as appropriate. - Input into the User Requirements Specification (URS) and co-oversight of Factory and Site Acceptance Testing (FAT/SAT). - Coordination of the execution of Installation Qualification (IQ
Save for later18/06/2024 | Fulltime | Lydney | MundipharmaManagement of nonconformances and resolution of issues with key stakeholders and/or the Qualified Person as appropriate. - Input into the User Requirements Specification (URS) and co-oversight of Factory and Site Acceptance Testing (FAT/SAT). - Coordination of the execution of Installation Qualification (IQ
Save for later18/06/2024 | Fulltime | Newent | MundipharmaOf the validation strategy following a risk-based approach as per ICH Q9 and ensuring regulatory and GMP requirements are met. - Prepare validations protocols in line with defined and approved validation strategy and company templates. - Management of nonconformances and resolution of issues with key stakeholders
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