FSP Scientist-Formulation & Process Development

Work Schedule

Environmental Conditions

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.
As a Scientist, your role will be to perform advanced diagnostic testing and analysis, ensure the accuracy and reliability of laboratory results, troubleshoot complex technical issues, and contribute to the continuous improvement of lab procedures and quality standards.

What You’ll Do:

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.

Knowledge, Skills and Abilities:

• 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 Safety

• Works 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…