Analytical Development Project Representative III

Work Schedule

Environmental Conditions

Job Description

As part of the Thermo Fisher Scientific team youll 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 worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

DESCRIPTION:
Join our team at Thermo Fisher Scientific as an R&D/Manufacturing Scientist III and make meaningful contributions to pharmaceutical this role youll be a part of a core team as the Analytical Chemistry SME and point of contact for complex technical projects involving formulation development process optimization and technology transfer for pharmaceutical products. Working with advanced analytical technologies technologies and equipment youll serve as a technical subject matter expert regarding method development and validation analytical testing and scientific problem-solving. This is client-facing role that consistently provides updates and solutions to clients and internal stakeholders to help advance drug development from pre-clinical through commercialization stages.

REQUIREMENTS:
Advanced degree plus 6 years of experience or Bachelors degree plus 10 years of pharmaceutical industry experience
Preferred Fields of Study: Chemistry Biochemistry Biology Pharmaceutical Sciences Engineering or related scientific field

Experience presenting scientific and technical information to clients and cross-functional teams
Expertise in analytical techniques including HPLC GC Karl Fischer spectroscopy and related instrumentation

Expertise in method development and method validation preferred.

Knowledge of USP/EP/JP compendials.

Proficiency and expertise with LIMS systems.

Preferred experience with scientific writing such as method validation protocols and reports.

Leading and documenting out of specification investigations with experience with lab incidents.
Strong knowledge of GMP requirements and pharmaceutical regulatory guidelines such as ICH
Demonstrated ability to manage multiple complex technical projects simultaneously
Strong data trending and ability to recognize and evaluate data trends
Proficiency with Microsoft Office applications and analytical software
Advanced problem-solving and troubleshooting abilities
Strong written and verbal communication skills
Experience supporting and developing team members through technical guidance
Physical requirements include standing/walking lifting up to 35 lbs and manual dexterity for lab work
Ability to work safely with laboratory chemicals and equipment while following SOPs