Analytical R&D Scientist II
at Thermo Fisher Scientific
Greenville, NC 27834, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 10 Nov, 2024 | Not Specified | 10 Aug, 2024 | N/A | Deliverables,Chemistry,Dissolution,Molecular Biology,Regulatory Compliance,Biochemistry,Oos,Disabilities,Raw Materials,Operations,Analytical Techniques,Spectroscopy,Empower,Research,Training | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
POSITION SUMMARY:
We are seeking a highly motivated and dedicated Analytical R&D Scientist II to join our exceptional team at Thermo Fisher Scientific Inc. As an Analytical R&D Scientist II, you will play a crucial role in our world-class research efforts, demonstrating a strong work ethic and commitment to excellence in biochemistry.
QUALIFICATIONS:
- Bachelor’s Degree in Chemistry, Biochemistry, Molecular Biology, or a related physical/biological science field, or equivalent experience.
- 3+ years of method development/validation experience (or 2+ years experience with a Master’s degree).
- Strong experience with HPLC.
- Experience with EMPOWER preferred.
Join our team and be part of Thermo Fisher Scientific Inc., a company dedicated to making the world healthier, cleaner, and safer. As an equal opportunity employer, we value diversity and strive to build an inclusive and collaborative work environment. We are committed to providing reasonable accommodations for applicants with disabilities during the job application process. Apply today at http://jobs.thermofisher.com.
Responsibilities:
- Validate test methods for pharmaceutical raw materials and finished products by using analytical techniques such as HPLC, GC, LC/MS, dissolution, spectroscopy, and compendial testing.
- Recognize and report out-of-specification or unexpected results, contributing to problem-solving and troubleshooting efforts.
- Write deviations, OOS, CAPA, Change Controls, SOP, and specification documents to ensure regulatory compliance.
- Develop validation, verification, and transfer protocols and implement them.
- Conduct instrument calibrations/verifications as required.
- Record and report analysis results, interpret data, and make recommendations based on findings.
- Research and assist with the implementation of new methods and processes to enhance operations.
- Manage projects, ensuring deliverables are met and next steps are identified.
- Collaborate with internal teams to meet project objectives and client expectations.
- Contribute to talent acceleration by training and mentoring Junior Scientists.
- Maintain compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines.
- Ability to function in a rapidly changing environment and balance multiple priorities.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Chemistry biochemistry molecular biology or a related physical/biological science field or equivalent experience
Proficient
1
Greenville, NC 27834, USA