Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Office

Job Description

Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission - to enable our customers to make the world healthier, safer, and cleaner.

Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to demonstrate the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.

• Completes pre-formulation, formulation and process development activities based on established protocols and procedures
• Assists in the manufacture of batches of product as the need arises, e.g. for process development, stability studies or clinical trials
• Coordinates activities within Pharmaceutical Development and with analytical and manufacturing representatives to meet project results
• Works with the team to align and implement pre-formulation, formulation and process development activities including authoring or contributing to manufacturing batch records
• Identify and begin to interpret any problems in the execution of experimental processes and/or in results and communicates them to 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 is trained independently with due regard for GMP and Safety
• 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 optimally and in compliance with departmental guidelines in a laboratory notebook or computer (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 their laboratory/working environment
• Maintains accurate and complete safety records consistent with company policy and legal requirements
• Recognizes potential safety problems and takes action to resolve them

• BS degree and 2-4 years of experience in an appropriate subject area or a MS with 0-2 years of experience.
• Is technically proficient in a number of formulation/process development techniques.
• Has good knowledge of GMP and GLP requirements, SOPs and policies
• Has operational knowledge of routine laboratory/plant equipment