mhra jobs in Manchester

Job Description Pharmacy Assistant – Manufacturing Full Time/18 month Fixed Term Contract (Maternity Cover) with a view to becoming permanent The Medicines Evaluation Unit, an IQVIA business is one of the UK’s leading contract research organisations conducting clinical trials for the pharmaceutical industry. The organisation holds MHRA Phase I Accreditation, together with an MHRA Manufacturing...

You will report to the Blood Sciences Service Manager.

You will ensure effective management of the blood transfusion department, which operates around the clock.

You will manage staffing, equipment, and consumables, providing professional leadership to Biomedical Scientist Team Managers, Biomedical Scientists and Pathology support staff.

You will lead core GCP quality activities including quality system oversight, audit planning and execution, and regulatory inspection readiness. This role offers the opportunity to influence quality strategy, shape inspection preparedness, and drive continuous improvement across a growing clinical portfolio.

You will report to the Blood Sciences Service Manager.

You will ensure effective management of the blood transfusion department, which operates around the clock.

You will manage staffing, equipment, and consumables, providing professional leadership to Biomedical Scientist Team Managers, Biomedical Scientists and Pathology support staff.

Salary: Up to £40k plus 20% bonus About Noumed: Noumed Life Sciences is an expanding global pharmaceutical company based in Maidenhead, Berkshire focusing on cGMP, solid dosage generic pharmaceuticals. Our passion lies in improving the quality of people’s lives through the development, manufacturing, and marketing of a diverse range of high-quality pharmaceutical products. In return for your...

You will play a key role in supporting the preparation, packaging, dispensing and quality control of pharmaceutical products. This management role combines accuracy with strict compliance to Good Manufacturing Practice (GMP) guidelines. What we are looking For…

You will report to the Blood Sciences Service Manager.

You will ensure effective management of the blood transfusion department, which operates around the clock.

You will manage staffing, equipment, and consumables, providing professional leadership to Biomedical Scientist Team Managers, Biomedical Scientists and Pathology support staff.

You will support a diverse range of clinical studies/trials involving patients and healthy volunteers, undertaking drug development programmes in a variety of therapeutic fields, including respiratory, dermatology, cardiovascular, endocrinology, and inflammatory disorders. Key responsibilities:To provide medical care and oversight of clinical trial participants.

You will support a diverse range of studies/trials specialising in research involving patients and healthy volunteers, primarily in respiratory research, as well as undertaking drug development programmes in a variety of other therapeutic fields.

You will be required to:· Provide a comprehensive data management support.

You will support a diverse range of clinical studies/trials involving patients and healthy volunteers, undertaking drug development programmes in a variety of therapeutic fields, including respiratory, dermatology, cardiovascular, endocrinology, and inflammatory disorders. Key responsibilities:To provide medical care and oversight of clinical trial participants.

You will support a diverse range of clinical studies/trials involving patients and healthy volunteers, undertaking drug development programmes in a variety of therapeutic fields, including respiratory, dermatology, cardiovascular, endocrinology, and inflammatory disorders. Key responsibilities:

You will support a diverse range of clinical studies/trials involving patients and healthy volunteers, undertaking drug development programmes in a variety of therapeutic fields, including respiratory, dermatology, cardiovascular, endocrinology, and inflammatory disorders. Key responsibilities:To provide medical care and oversight of clinical trial participants.

Pharmacy Assistant Manufacturing Full Time/18 month Fixed Term Contract (Maternity Cover) with a view to becoming permanent The Medicines Evaluation Unit, an IQVIA business is one of the UKs leading contract research organisations conducting clinical trials for the pharmaceutical industry.The organisation holds MHRA Phase I Accreditation, together with an MHRA Manufacturing Licence MIA (IMP)....

You will support a diverse range of studies/trials specialising in research involving patients and healthy volunteers, primarily in respiratory research, as well as undertaking drug development programmes in a variety of other therapeutic fields.

You will be required to:· Provide a comprehensive data management support.

Pharmacy Assistant – Manufacturing Full Time/18 month Fixed Term Contract (Maternity Cover) with a view to becoming permanent The Medicines Evaluation Unit, an IQVIA business is one of the UK’s leading contract research organisations conducting clinical trials for the pharmaceutical industry. The organisation holds MHRA Phase I Accreditation, together with an MHRA Manufacturing Licence MIA...

You will support a diverse range of clinical studies/trials involving patients and healthy volunteers, undertaking drug development programmes in a variety of therapeutic fields, including respiratory, dermatology, cardiovascular, endocrinology, and inflammatory disorders. Key responsibilities: To provide medical care and oversight of clinical trial participants.

You will support a diverse range of studies/trials specialising in research involving patients and healthy volunteers, primarily in respiratory research, as well as undertaking drug development programmes in a variety of other therapeutic fields.

You will be required to: Provide a comprehensive data management support.

You will support a diverse range of studies/trials specialising in research involving patients and healthy volunteers, primarily in respiratory research, as well as undertaking drug development programmes in a variety of other therapeutic fields.

You will be required to:· Provide a comprehensive data management support.

You will play a key role in supporting the preparation, packaging, dispensing and quality control of pharmaceutical products. This management role combines accuracy with strict compliance to Good Manufacturing Practice (GMP) guidelines. What we are looking For…

You will support a diverse range of studies/trials specialising in research involving patients and healthy volunteers, primarily in respiratory research, as well as undertaking drug development programmes in a variety of other therapeutic fields.

You will be required to:· Provide a comprehensive data management support.