MSAT Technical Transfer Scientist II Full-time

Msat Tt Scientist Ii

As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Join our team as an MSAT TT Scientist II at Thermo Fisher Scientific, where you'll contribute to pharmaceutical research and development. You'll perform complex analytical testing, develop and validate methods, and ensure product quality while collaborating with cross-functional teams. This role offers the opportunity to work with advanced technology and contribute to life-changing healthcare solutions. You'll conduct sophisticated chemical and physical testing, lead technology transfer activities, and support manufacturing operations. Working closely with internal teams and clients, you'll help advance pharmaceutical development while maintaining the highest standards of quality and compliance.

Technically supports day-to-day operations in the Formulation, Filling, and/or Freeze Drying areas of the Steriles plant.

Works on technical/scientific process/product/project activities to implement strategies and technical solutions.

Assists in the creation of processes, single use systems, and equipment designs for clinical, scale up, and/or registration batches, including technology transfer of projects from clients.

Makes decisions that involve direct application of technical knowledge.

Complete studies, tech transfer, commercial scale-up and support process validation.

Represent the organization on internal technical discussions.

Actively participate in problem solving and project results for formulations, equipment and processes.

Write/revise work orders for existing processes, FORMs, reports, memos, and protocols.

Lead projects with a moderate level of supervision, implement change control actions, review and plans technical aspects of the project to meet timeline and project goals.

Support manufacturing operations, change controls, investigations as subject matter expert (SME).

Collects data for statistical analysis. Can support interpretation and summary of data.

Requirements:

• Advanced Degree, no prior experience required, or Bachelor's Degree plus 2 years of experience in pharmaceutical or related industry, preferably in GMP/GLP environment

• Preferred Fields of Study: Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or related physical science field

• Extensive hands-on experience with analytical instrumentation including HPLC, GC, LC/MS, spectroscopy, and dissolution testing

• Strong knowledge of pharmaceutical GMPs, regulatory requirements, and quality systems

• Proven expertise in method development, validation, and transfer of analytical methods

• Experience with data analysis, interpretation, and technical writing of protocols and reports

• Proficiency in Microsoft Office Suite and analytical software systems

• Strong analytical and problem-solving capabilities

• Demonstrated project management abilities and capacity to manage multiple projects

• Effective written and verbal communication skills for both technical and non-technical audiences

• Ability to work both independently and collaboratively

• Physical requirements include standing for extended periods, lifting up to 35 pounds, and working with laboratory equipment

• Must be able to follow safety protocols and wear appropriate PPE as required

• Demonstrated alignment with company values of Integrity, Intensity, Innovation, and Involvement