Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.)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 MSAT TT Scientist III and make meaningful contributions to pharmaceutical this role youll lead complex technical projects involving formulation development process optimization and technology transfer for pharmaceutical products. Working with advanced analytical technologies and equipment youll develop and validate scientific methodologies while ensuring compliance with GMP standards. Youll serve as a technical subject matter expert collaborating with cross-functional teams and clients to implement innovative solutions that advance drug development from pre-clinical through commercialization stages.
Discover Impactful Work
Technically supports day-to-day operations in the Formulation Filling and/or Freeze Drying areas of the Steriles plant.
Leads technical/scientific process/product/project activities to implement strategies and technical solutions.
Drives 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.
A Day in the Life
Design implement and evaluate studies lead tech transfer commercial scale-up and support process validation.
Represent the organization on formal technical and scientific forums.
Lead and/or participate in problem solving and project work for formulations equipment and processes.
Write/revise work orders for new processes FORMs reports memos and protocols as required.
Independently manage projects proficient in evaluating and organizing all technical aspects of the project to achieve necessary landmarks and turning points.
Support manufacturing operations change controls investigations as subject matter expert (SME) resolve accurate CAPAs.
Assess material changes and determine change impact.
Support development of proposals and timelines for projects leading relevant client meetings.
Review new bid quotes protocols technical documents results and reports.
REQUIREMENTS:
Advanced degree plus 3 years of experience or Bachelors degree plus 5 years of pharmaceutical industry experience
Preferred Fields of Study: Chemistry Biochemistry Biology Pharmaceutical Sciences Engineering or related scientific field
Expertise in analytical techniques including HPLC GC LC/MS spectroscopy and related instrumentation
Strong knowledge of GMP requirements and pharmaceutical regulatory guidelines
Experience with method development validation and technology transfer
Demonstrated ability to manage multiple complex technical projects simultaneously
Excellent documentation skills for technical reports protocols and regulatory submissions
Strong data analysis and statistical evaluation capabilities
Experience presenting technical information to clients and cross-functional teams
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
Experience in a contract manufacturing organization (CMO) preferred
Knowledge of aseptic techniques and sterile manufacturing preferred for some positions
Required Experience:
IC
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