You will use your scientific and technical formulation expertise to develop formulations from idea to proven technology / asset.Based in our Nottingham Technical Centre, this is a full-time, one-year fixed term laboratory-based role.
Working in the Prototyping Team and reporting to the Prototyping Formulation Manager, you will be part of the wider Formulation/Product Development Team in the R&D and Supply Chain function of the No7 Beauty Company.You will work with other Formulation Technologists, Technicians and Raw Material Specialists from your own team, as well as Formulators, Testing, Quality, Safety, Regulatory, Packaging and Project Managers from other teams.
You will use your scientific and technical formulation expertise to develop formulations from idea to proven technology / asset.Based in our Nottingham Technical Centre, this is a full-time, permanent laboratory-based role.
Working in the Prototyping Team and reporting to the Prototyping Formulation Manager, you will be part of the wider Formulation/Product Development Team in the R&D and Supply Chain function of the No7 Beauty Company.You will work with other Formulation Technologists, Technicians and Raw Material Specialists from your own team, as well as Formulators, Testing, Quality, Safety, Regulatory, Packaging and Project Managers from other teams.
IT Product Manager - Projects, General Accounting and Finance Clinical SupplyThe S/4HANA - IT Product Manager owns the technical solution design for the Projects, General Accounting and Finance Clinical Supply capability or part of a cross-functional component.
The role is a key position on the Axial Programme IT design team, taking a central role in defining the global design template for AstraZeneca in line with our ambition of Fit to Standard using SAP best practice as far as possible.
You will be a member of a wider Axial IT Design Team that will lead in defining the IT solution that will support our global standardised business processes.
Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.
This opportunity is for a QC Analytical Validation Specialist to join the QC Technical Services Team on a contract basis.
Ensures that the labeling strategy is aligned with the overall product regulatory, registration, commercial and development strategy.
The Associate Director, Global Labeling Strategy The Associate Director, Global Labeling Strategy for Early Asset has overall accountability for initial creation and relevant updates to labeling documents (Target Label Profile (TLP), Company Core Data Sheet (CCDS), United States Package Inserts (USPI) and EU Summary of Product Characteristics (SmPC) for products registered via the centralized, Mutual Recognition or Decentralized Procedure.
Drive the labeling strategy to early development activities to ensure consideration of labeling in claims development programs.
Do you have hands on experience in using techniques such as Balances, pH meter, UV, Karl Fisher, FT-IR, TLC, Dissolution and HPLC (to include degradation analysis)?
Does your experience include hands on analytical testing of finished drug products?
Are you currently working in analytical quality control?