formulation scientist pharma jobs in West Yorkshire

You will own outcomes across discovery, delivery, and iteration, ensuring our solutions reflect real scientific workflows in pharmaceutical and chemical domains and create measurable value for members and regulators.

You will own outcomes across discovery, delivery, and iteration, ensuring our solutions reflect real scientific workflows in pharmaceutical and chemical domains and create measurable value for members and regulators.

Drive growth. Build partnerships. Shape the future of peptide innovation. Biosynth is a trusted global partner securing the supply chains of the life sciences and pharmaceutical industries. With over one million research products and extensive manufacturing capabilities across complex chemicals, peptides, and biological materials, we help our partners bring breakthroughs to life. Headquartered...

HEOR Scientist, Pneumococcal Vaccines Note - To be successful in this role, the candidate must bring extensive HEOR and real-world evidence expertise, ideally with around 10 years of experience in consultancy, CRO, or global pharma settings. Strong knowledge of vaccines (or immunology as a close alternative) is essential to quickly adapt to the therapeutic area and deliver impactful evidence...

You will be responsible for the Statistical Genetics work required to support an asset being taken through late-stage trials. Major responsibilities will include (but are not limited to): - Formulate a genomics strategy for advancing late-stage therapeutic programs - Lead generation of WGS and other omics data within clinical trials

Principal Medical Writer, Clinical Development Our client is a Biotech company with a strong pipeline, now wish to hire a Principal Medical Writer within their Clinical Development team, working closely with functional teams e.g. Clinical Operations, Regulatory Affairs, Medical Affairs, Commercial, etc. The successful candidate will author, review and manage clinical documents, e.g., clinical...

You will have significant in-depth practical experience in designing and delivering full shopfloor to cloud data integration projects using one or more of the main vendor’s product suites. - Demonstrable experience in relevant manufacturing/process/logistics industries.

You will have the flexibility you need to do your best work with hybrid work options.

Medical Writing Manager Our client is a Biotech company with a strong pipeline, now wish to hire a Medical Writing Manager working closely with functional teams e.g. Regulatory Affairs, Medical Writing, Clinical Operations, Medical Affairs, etc. The successful candidate will author, review and manage clinical documents, e.g., clinical study protocols and/or amendments, investigator brochures,...

You will be responsible for the Statistical Genetics work required to support an asset being taken through late-stage trials. Major responsibilities will include (but are not limited to): - Formulate a genomics strategy for advancing late-stage therapeutic programs - Lead generation of WGS and other omics data within clinical trials

HEOR Scientist, Pneumococcal Vaccines Note - To be successful in this role, the candidate must bring extensive HEOR and real-world evidence expertise, ideally with around 10 years of experience in consultancy, CRO, or global pharma settings. Strong knowledge of vaccines (or immunology as a close alternative) is essential to quickly adapt to the therapeutic area and deliver impactful evidence...

Drive growth. Build partnerships. Shape the future of peptide innovation. Biosynth is a trusted global partner securing the supply chains of the life sciences and pharmaceutical industries. With over one million research products and extensive manufacturing capabilities across complex chemicals, peptides, and biological materials, we help our partners bring breakthroughs to life. Headquartered...

You will own outcomes across discovery, delivery, and iteration, ensuring our solutions reflect real scientific workflows in pharmaceutical and chemical domains and create measurable value for members and regulators.

Drive growth. Build partnerships. Shape the future of peptide innovation. Biosynth is a trusted global partner securing the supply chains of the life sciences and pharmaceutical industries. With over one million research products and extensive manufacturing capabilities across complex chemicals, peptides, and biological materials, we help our partners bring breakthroughs to life. Headquartered...

Principal Medical Writer, Clinical Development Our client is a Biotech company with a strong pipeline, now wish to hire a Principal Medical Writer within their Clinical Development team, working closely with functional teams e.g. Clinical Operations, Regulatory Affairs, Medical Affairs, Commercial, etc. The successful candidate will author, review and manage clinical documents, e.g., clinical...

You will be responsible for the Statistical Genetics work required to support an asset being taken through late-stage trials. Major responsibilities will include (but are not limited to): - Formulate a genomics strategy for advancing late-stage therapeutic programs - Lead generation of WGS and other omics data within clinical trials

HEOR Scientist, Pneumococcal Vaccines Note - To be successful in this role, the candidate must bring extensive HEOR and real-world evidence expertise, ideally with around 10 years of experience in consultancy, CRO, or global pharma settings. Strong knowledge of vaccines (or immunology as a close alternative) is essential to quickly adapt to the therapeutic area and deliver impactful evidence...

Drive growth. Build partnerships. Shape the future of peptide innovation. Biosynth is a trusted global partner securing the supply chains of the life sciences and pharmaceutical industries. With over one million research products and extensive manufacturing capabilities across complex chemicals, peptides, and biological materials, we help our partners bring breakthroughs to life. Headquartered...

You will be responsible for the Statistical Genetics work required to support an asset being taken through late-stage trials. Major responsibilities will include (but are not limited to): - Formulate a genomics strategy for advancing late-stage therapeutic programs - Lead generation of WGS and other omics data within clinical trials

Medical Writing Manager Our client is a Biotech company with a strong pipeline, now wish to hire a Medical Writing Manager working closely with functional teams e.g. Regulatory Affairs, Medical Writing, Clinical Operations, Medical Affairs, etc. The successful candidate will author, review and manage clinical documents, e.g., clinical study protocols and/or amendments, investigator brochures,...

Medical Writing Manager Our client is a Biotech company with a strong pipeline, now wish to hire a Medical Writing Manager working closely with functional teams e.g. Regulatory Affairs, Medical Writing, Clinical Operations, Medical Affairs, etc. The successful candidate will author, review and manage clinical documents, e.g., clinical study protocols and/or amendments, investigator brochures,...