R&D Mfg Scientist III Analytical Development
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Job Location:
Greenville, NC - USA
Monthly Salary:
Not Disclosed
Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Laboratory Setting Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Will work with hazardous/toxic materialsJob 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 in Analytical Development 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.
REQUIREMENTS:
Bachelors degree in Chemistry Biochemistry Biology Pharmaceutical Sciences Engineering or related scientific field plus 5 years of pharmaceutical lab experience
Advanced degree plus 3 years of pharmaceutical lab experience
Expertise in analytical techniques including HPLC GC LC/MS spectroscopy and related instrumentation
Experience with method development validation and technology transfer
Experience presenting technical information to clients and cross-functional teams
Experience supporting and developing team members through technical guidance
Experience in a contract manufacturing organization (CMO) preferred
Knowledge Skills Abilities:
Strong knowledge of GMP requirements and pharmaceutical regulatory guidelines
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
Proficiency with Microsoft Office applications and analytical software
Advanced problem-solving and troubleshooting abilities
Strong written and verbal communication skills
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
Knowledge of aseptic techniques and sterile manufacturing preferred for some positions
Required Experience:
IC
Key Skills
- Laboratory Experience
- Vendor Management
- Design Controls
- C/C++
- FDA Regulations
- Intellectual Property Law
- ISO 13485
- Research Experience
- SolidWorks
- Research & Development
- Internet Of Things
- Product Development
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more
