FSP Scientist-Formulation & Process Development
FSP Scientist-Formulation & Process Development
Posted 6 days ago
SENIORITY
Senior
About the role
- To utilise technical skills and expertise to develop drug product formulations and associated manufacturing processes as part of a matrix Technical Team. Conduct duties as listed below, plus any other tasks as requested by team leader or departmental director.
- Work as part of a multi-disciplinary development team, liaising efficiently with Formulators, Modellers, Process Analytical Technology (PAT) Scientists, automation experts, data scientists and device engineers, to plan and Execute preformulation, formulation and process development activities
- Assists in the manufacture of batches of product as required, e.g. for process development, stability studies or clinical trials
- Coordinates his/her activities within Pharmaceutical Development and with analytical and manufacturing representatives to meet project deliverables
- Works with the matrix technical team to align and execute preformulation, formulation and process development activities including authoring or contributing to manufacturing batch records
- Identify and interpret any problems in the execution of experimental processes and/or in results and communicates them to his/her supervisor
- Proactively engage and seek assistance from other scientists to solve problems
- Maintains cleanliness in own work area and in communal work areas
- Anticipates/recognizes potential problems with equipment and/or supplies, and proposes/initiates action to solve or prevent problems
- Operates equipment for which he/she is trained independently with due regard for GMP and SafetyWorks to GMP/GLP as appropriate
- Demonstrates timely & reliable recording of laboratory data in Labware and other suitable systems in accordance with company policy and legal requirements.
- Performs data management tasks including recording results effectively and in compliance with departmental guidelines in a laboratory notebook or computer with minimal supervision (e.g. tabulating and graphing results)
- Consults with supervisor when difficulties arise that cannot be readily resolved
- Prepares oral or written summaries of results with interpretation for project work
- Writes specific technical sections of internal and external reports with supervision
- Attends regular safety training and is fully aware of safety requirements for his/her laboratory/working environment
- Follows safe Laboratory and Manufacturing Practices
- Maintains accurate and complete safety records consistent with company policy and legal requirements
- Recognizes potential safety problems and takes action to rectify them
- Can perform literature searches independently and understands scientific literature directly related to his/her experiments
- Can learn and apply new experimental techniques
- Has basic knowledge about regulatory requirements for sterile and oral solid dosage forms
- Working Conditions and Environment:
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