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Covers leading and managing independent studies, designing, planning, and executing stability-focused analytical work to support biotherapeutics, including SEC, RP-HPLC, CEX, HPAE, UV, DLS, and ELISA. Requires technical line management, stability regulatory knowledge, data analysis/reporting, SOP compliance, quality control/assurance leadership, budgeting input, stakeholder updates, and resolution of project issues. 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To independently lead, design, plan and manage own studies as required to achieve objectives and those of Arecor Stakeholders  \n2. In depth knowledge of analytical methods such as SEC, RP-HPLC, CEX, HPAE, UV, DLS, ELISA etc as required to demonstrate the stability of biotherapeutics.  \n3. To line manage technical development staff as required  \n4. Experience and/or understanding of stability related regulatory guidelines.  \n5. Represent Arecor at project team meetings and provide expert technical advice to Stakeholders.  \n6. To execute, analyse and report data to the standards expected by Arecor and associated stakeholders.  \n7. Perform routine duties as required in the relevant laboratory section in order to ensure the timely generation of accurate data and information.  \n8. Ensure all activities follow standard operating procedures and/or protocols as required.  \n9. Represent the company at external seminars , conferences and supplier visits as required.  \n10. Input into budgets related to projects and department as required  \n11. Provide regular updates on all assigned projects to relevant stakeholders  \n12. Work with other departments to resolve issues and implement corrective actions.  \n13. Maintain and develop state of the art knowledge applicable to existing and future processes and maintain up-to-date knowledge on formulation sciences and associated IP.  \n14. Ensuring that all interactions and engagements are carried out with the highest ethical and professional standards and that all work is accomplished with the highest quality.  \n15. To drive and maintain laboratory Quality Control and Quality Assurance to the required standard.  \n16. To follow health and safety guidelines as issued by the Company  \n17. Carry out other reasonable tasks as required by the Line Manager.  \nThe above duties and responsibilities are not an exhaustive list and you may be required to undertake any other reasonable duties compatible with your experience and competencies. This description may be varied from time to time to reflect changing business requirements.  \nPrincipal Relationships  \n1. Accountable to Line Manager.  \n2. Responsible for Client and internal development projects as required.  \n3. Liaise with internal personnel at all levels of the business as required.  \n4. Liaise with external third parties as required.  \nEducation & Experience  \n• The job holder should be educated too PhD or Degree level in a scientific discipline  \n• The job holder should have 3+ years’ experience in a pharmaceutical product development or scientific setting  \n• Communication, planning, team working and organisational skills essential  \n• Experience of formulation sciences advantageous  \nSkills and Attributes  \n1. Competent and organised self-starter with the ability to perform multiple tasks concurrently.  \n2. Ability to work closely with others, encourage good team spirit, motivate a multi-skilled team to higher goals and demonstrate initiative as required.  \n3. A flexible and willing attitude with the desire to continually improve and develop both self and junior colleagues.  \n4. Strong communication skills with the ability to deliver and follow instructions and guidance.  \n5. Methodical, organised with an aptitude for detail.  \n6. Able to take responsibility and give direction as required.  \n7. To maintain Arecor company values at all times  \nIssued by:   Date:    \nManager  \nAccepted by:   Date:    \nJob Holder – Insert name","cbCaioBplSZHspPT","https://ap.wps.com/l/cbCaioBplSZHspPT","pdf",93716,"English","# Principal Responsibilities\n## Broad Function\n## Principal Relationships\n## Education & Experience\n## Skills and Attributes\n## Compliance and Additional Duties","[{\"question\":\"What is the broad function of the Senior Scientist role?\",\"answer\":\"To perform general duties and lead project work within the relevant laboratory section of the Development Department.\"},{\"question\":\"Which analytical methods are referenced for demonstrating biotherapeutics stability?\",\"answer\":\"SEC, RP-HPLC, CEX, HPAE, UV, DLS, and ELISA are listed as required methods.\"},{\"question\":\"What responsibilities relate to quality and compliance?\",\"answer\":\"The role includes driving laboratory Quality Control and Quality Assurance to the required standard, ensuring activities follow SOPs/protocols, and following company health and safety guidelines.\"}]","Senior Scientist Job Description - Development Department | PDF",1789357866]