Labs FSP - Research Scientist - qPCR, Genomics, NGS
at Thermo Fisher Scientific
Lawrenceville, New Jersey, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Jul, 2024 | Not Specified | 05 May, 2024 | 8 year(s) or above | Rna,Statistical Tools,Diverse Groups,Technology,Wellbeing,Cgmp Manufacturing,Ngs,Regulatory Guidelines,Sequel,Training,Perkin Elmer,Molecular Biology,Analytical Support,Office Equipment,Cell Therapy,Genetics,Microbiology,Jmp | 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:
JOB DESCRIPTION
Thermo Fisher’s clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner.
EDUCATION
- Bachelor’s degree in microbiology or molecular biology, genetics or equivalent and relevant formal academic / vocational qualification
EXPERIENCE
- Pevious experience that provides the knowledge, skills, and abilities to perform the job: comparable to 8+ years
- In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
KNOWLEDGE, SKILLS, AND ABILITIES:
- Experience with NGS is a highly preferred skill (e.g., Illumina, nanopore, next seq, nova seq, hi seq, SMRT sequencing, Sequel, HiFi sequencing etc.).
- Previous hand on experience with handling human DNA and RNA, working with and troubleshooting automated workflows utilizing systems such as Tecan and Perkin-Elmer, Applied Biosystems, Affymetrix and Illumina (7900, Viia7, Quant-Studio, MiSeq, NextSeq) software is strongly preferred.
- Experience of using JMP or similar statistical tools is plus
- Hands-on experience and In-depth knowledge of in-vitro cell-based potency assays
- Experience in Gene and Cell therapy is desirable
- Knowledge of relevant ICH and regulatory guidelines and good understanding of GMP concept.
- Experience with analytical support for late-stage or commercial biological products and cGMP manufacturing
- Ability to prioritize objectives from multiple projects and adhere to scheduled timelines while maintaining flexibility and efficiency
Responsibilities:
ESSENTIAL FUNCTIONS:
- MUST HAVE: Next-Generation Sequencing (NGS) and Microbiology background
- Work independently or in collaboration with internal and/or external partners in analytical lifecycle activities including method development, validation, and method transfer
- Be a key Subject Matter Expert (SME) and represent ASAT to participate in troubleshooting and OOS investigation occurred during release and/or stability testing
- Provide SME assessment for deviation, CAPA and change control
- Participate in internal and external meeting
- Author and/or review technical documents, including method SOP, study protocol and technical report
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
- Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
- Able to work upright and stationary and/or standing for typical working hours.
- Able to lift and move objects up to 25 pounds.
- Able to work in non-traditional work environments.
- Able to use and learn standard office equipment and technology with proficiency.
- May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
- Able to perform successfully while prioritizing and handling multiple projects or activities
REQUIREMENT SUMMARY
Min:8.0Max:13.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Microbiology or molecular biology genetics or equivalent and relevant formal academic vocational qualification
Proficient
1
Lawrenceville, NJ, USA