Posted in Science and Research
Work Schedule
First Shift (Days)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
Job Description
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 clients to make the world healthier, safer, and cleaner.
Within our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use 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.
As a Scientist III you will performs complex laboratory analysis of pharmaceutical products and proficiently use analytical instrumentation, calculate and analyzes data and record data in adherence with Thermo Fisher/PPD SOP's and the industry.
Knowledge, Skills and Abilities
• Bachelor's Degree in Biochemistry, Molecular Biology, Genetics, Biotechnology,
Bioengineering, or a related scientific field with 4+ years of experience. Master's Degree with 2+ years of experience.
-In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
• Strong hands-on experience with different purification techniques such as
chromatography (RP-HPLC) and tangential flow filtration (TFF) and associated
instrumentation such as AKTA chromatography systems and Unicorn software.
• Design and execute DOE studies & high-throughput screen for purification process
improvements and advancements including parameter optimization, scale-up,
process window determination and process capability evaluation
• Understand experimental design and be able to independently execute laboratory
experiments.
• Communicate effectively with regular verbal and formal updates to project teams and
management.
• Proficiency in English is a must
• Understanding of purification of biologics, specifically large size mRNA, including
process scale-up.
• Relevant specific expertise in mRNA purification or very broad & deep expert-level
experience & understanding of purification of biomolecules
• Experience and understanding of nucleic acid analytical technologies.
• Understanding of Quality by Design and the development of a process control
strategy.
Working Environment:
PPD values the health and well being of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
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