Walker Cole International is supporting a pharmaceutical organisation based in the West Midlands, in the search for a Quality Manager/ RP to oversee GDP and GMP Quality systems across wholesale distribution and importation activities. This role carries regulatory responsibility and plays a key part in ensuring licence compliance, operational excellence and continuous improvement across a regulated pharmaceutical supply environment. Key Responsibilities Act as the Responsible Person (RP) in accordance with Human Medicines Regulations, ensuring full GDP compliance. Oversee WDA and associated licence requirements, including controlled drug compliance where applicable. Lead and maintain the Quality Management System, including deviations, CAPA, change control and risk management processes. Manage quality oversight of outsourced partners and suppliers, including audit activities and GMP compliance support. Requirements Eligibility to act as a UK Responsible Person (RP). Strong working knowledge of GDP and sound understanding of GMP principles. Experience developing or maintaining a Pharmaceutical Quality Management System within a regulated environment. Ability to operate autonomously, influence stakeholders and drive continuous quality improvement. Quality Manager Responsible Person RP GDP GMP WDA QMS Deviations CAPA Change Control Supplier Audits Regulatory Compliance Pharmaceutical Distribution Quality Leadership 96302
Feb 28, 2026
Full time
Walker Cole International is supporting a pharmaceutical organisation based in the West Midlands, in the search for a Quality Manager/ RP to oversee GDP and GMP Quality systems across wholesale distribution and importation activities. This role carries regulatory responsibility and plays a key part in ensuring licence compliance, operational excellence and continuous improvement across a regulated pharmaceutical supply environment. Key Responsibilities Act as the Responsible Person (RP) in accordance with Human Medicines Regulations, ensuring full GDP compliance. Oversee WDA and associated licence requirements, including controlled drug compliance where applicable. Lead and maintain the Quality Management System, including deviations, CAPA, change control and risk management processes. Manage quality oversight of outsourced partners and suppliers, including audit activities and GMP compliance support. Requirements Eligibility to act as a UK Responsible Person (RP). Strong working knowledge of GDP and sound understanding of GMP principles. Experience developing or maintaining a Pharmaceutical Quality Management System within a regulated environment. Ability to operate autonomously, influence stakeholders and drive continuous quality improvement. Quality Manager Responsible Person RP GDP GMP WDA QMS Deviations CAPA Change Control Supplier Audits Regulatory Compliance Pharmaceutical Distribution Quality Leadership 96302
My client, a Pharmaceutical company in Essex is looking for 2 QC analysts to join theire already established team. The QC Laboratory Analysts are responsible for conducting Quality Control testing and documenting laboratory testing in accordance with the MHRA and EU GMP Guidelines. You will also be responsible for performing and assisting in the OOS investigations where required. KEY RESPONSIBILITIES: Involvement in the control of Standard Operating Procedures. Planning testing workload under the supervision. Performing laboratory tests to produce reliable and precise data / results. Complying with the Company Standard Operating Procedures (SOP s) Complying with GMP and carrying out routine tasks accurately and following strict methodologies to carry out analyses. Complying with company Health & Safety Policy and Procedures. To carry out any ad hoc duties as required. Ensuring laboratory test record data is recorded and stored in real time and in compliance to data integrity. Preparing samples, standards and reagents according to the relevant procedures. Maintain all areas other associated with laboratory in a presentable condition ready to being audited at any time. Performing method validations / method transfers where needed. Maintaining and operating standard laboratory equipment, for example titrators, pH meters etc. Assisting the Quality Team as directed. Assisting senior management in writing of validation protocols and linked reports. Ensuring the laboratory is well-stocked for performing the tests. Participating in self-inspections and regulatory inspections. For a full JD and immediate consideration, please reach out ASAP!
Feb 27, 2026
Full time
My client, a Pharmaceutical company in Essex is looking for 2 QC analysts to join theire already established team. The QC Laboratory Analysts are responsible for conducting Quality Control testing and documenting laboratory testing in accordance with the MHRA and EU GMP Guidelines. You will also be responsible for performing and assisting in the OOS investigations where required. KEY RESPONSIBILITIES: Involvement in the control of Standard Operating Procedures. Planning testing workload under the supervision. Performing laboratory tests to produce reliable and precise data / results. Complying with the Company Standard Operating Procedures (SOP s) Complying with GMP and carrying out routine tasks accurately and following strict methodologies to carry out analyses. Complying with company Health & Safety Policy and Procedures. To carry out any ad hoc duties as required. Ensuring laboratory test record data is recorded and stored in real time and in compliance to data integrity. Preparing samples, standards and reagents according to the relevant procedures. Maintain all areas other associated with laboratory in a presentable condition ready to being audited at any time. Performing method validations / method transfers where needed. Maintaining and operating standard laboratory equipment, for example titrators, pH meters etc. Assisting the Quality Team as directed. Assisting senior management in writing of validation protocols and linked reports. Ensuring the laboratory is well-stocked for performing the tests. Participating in self-inspections and regulatory inspections. For a full JD and immediate consideration, please reach out ASAP!
