Deviation Specialist II (12 hour days)
Share
Job Location:
Greenville, NC - USA
Monthly Salary:
Not Disclosed
Posted on:
8 hours ago
Vacancies:
1 Vacancy
Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob 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 as an R&D/Manufacturing Scientist II at Thermo Fisher Scientific where youll contribute to pharmaceutical research and development. Youll 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. Youll conduct sophisticated chemical and physical testing lead technology transfer activities and support manufacturing operations. Working closely with internal teams and clients youll help advance pharmaceutical development while maintaining the highest standards of quality and compliance.
** Typical Working hours are 6:00am-6:00pm on a 2-2-3 shift rotation.
REQUIREMENTS:
Advanced Degree no prior experience required or Bachelors 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
Required Experience:
IC
Key Skills
- Sales Experience
- Crane
- Customer Service
- Communication skills
- Heavy Equipment Operation
- Microsoft Word
- Case Management
- OSHA
- Team Management
- Catheterization
- Microsoft Outlook Calendar
- EHS
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
