Analytical Development Scientist II

As the world leader in serving science, our work is more than something that fills our days – what we do has great purpose. Our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research to clinical to commercial production means you can have a broad and meaningful impact here at Thermo Fisher Scientific. All while working in an environment where you will be supported, valued and rewarded for your performance.

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or the development and manufacture of life-changing therapies, we are here to support them. Our global team of more than 100,000 colleagues delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

ANALYTICAL DEVELOPMENT SCIENTIST II

Job Description

We are seeking an energetic and enthusiastic individual with strong communication, leadership, technical and operational skills to join our growing BioProcess Sciences (BPS) team.

How will you make an impact?

In BPS, our goal is to develop, characterize and scale-up bioprocesses for robust manufacture of viral vectors to help our clients deliver lifesaving therapies to patients.

As a Scientist II in analytical development (AD), you will plan, design, execute, and document analytical testing and method transfer activities. You will also act as domain expert in analytical development for viral vector while supporting detailed transfer and development of analytical methods from clients into Bioprocess Sciences lab. You will also be supporting assay transfer out to the QC for cGMP testing.

This is a hands-on position. The ideal candidate shall have excellent lab skills, strong documentation skills, ability to analyze and summarize data to draw conclusions, make recommendations, and tight-knit collaboration skills.

What will you do?

• As a bench scientist, independently support the development, validation, assessment and execution of one or more analytical methods that is grounded in Biophysics and Physiochemistry e.g. analytical ultracentrifugation, dynamic light scanning, Raman spectroscopy, mass photometry, etc. (60% of the time)

• Mentor and coach junior team members

• Independently develop, revise and review SOPs, work instructions, test record, test report

• Independently support technology transfers from R&D to QC and/or from client to BPS

• Work closely with R&D, manufacturing, quality and project management teams to execute assays that meet customer and manufacturing needs in support of department, site, and corporate objectives

• Independently analyze data, present results and conclusions to the team

• Responsible for some lab management tasks

• Apply principles and practice of quality improvement

• Keep current on Environment, Health & Safety policies, ensure safe environmental and working conditions in the Analytical Sciences labs

How will you get here?

• B.S. with 3 yrs., Masters degree with 1 year experience, or PhD in Chemistry, Biochemistry, Engineering or related field

Experience, skills and abilities

• Experience with analytical assays for biophysical characterization in the Gene and/or cell therapy modalities is preferred.

• Knowledge and experience with chemistry, analytical chemistry, biophysics, is highly desirable.

• Broad technical proficiency, ability to solve complex issues independently and as a part of a team.

• Significant laboratory documentation experience.

• Familiar with GLP requirements; some knowledge of cGMP requirements of biopharmaceutical manufacturing.

• Ability to function in a rapidly changing environment & handle multiple priorities.

• An onsite, flexible work schedule is required.

• Ability to lift up to 25 lbs.

While performing the duties of this job, the employee

• Will work in a dynamic environment and balance multiple priorities simultaneously!

• Will be self-motivated and proactively drive efficient execution.

• Will be encouraged to learn new software, processes, and tools quickly!

• Will use outstanding equipment and instrumentation in daily manufacturing.

• Will demonstrate flexibility with changes to working environment and deliver high quality results.

• Will critically review processes and recommend improvements to supervisor/manager.

At Thermo Fisher Scientific, each one of our 100,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner, and safer.