Lab Supervisor

at  Thermo Fisher Scientific

Alachua, Florida, USA - 00000

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate12 Oct, 2021Not Specified12 Jun, 20213 year(s) or aboveExperimental Design,Molecular Biology,Color,Viral Vectors,Cell Culture,BiochemistryNoNo
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Requisition ID:163546BR
When you join us at Thermo Fisher Scientific, you’ll be part of a smart, driven team that shares your passion for exploration and discovery! With revenues of more than $24 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.


A Bachelor’s degree in an appropriate area of specialization (molecular biology, biochemistry, engineering etc.) with 3+ years proven experience; or Masters or Ph.D in an appropriate area of specialization without proven or industry experience.


  • Laboratory experience (ie, cell culture, viral vectors)
  • Experimental design (ie, process development)
  • Analyzing and presenting data


  • Leading and supporting a team
  • Managing multiple projects
  • Problem solving and critical thinking
    At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.
    Apply today!
    Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status


You will lead and support Upstream Process Development (PD) activities that enables VVS to deliver a scalable manufacturing process to its clients for the purpose of producing viral vector material for clinical use. This will include active involvement in the vector production process and researching/sourcing reagents, equipment and materials for specific activities related to the process.

  • Work closely with Manufacturing personnel to ensure that the process developed in PD is successfully transitioned to clinical Manufacturing.
  • Collaborate with the Upstream PD team and clients in the design, modify and scale-up of processes to ensure their successful scalability and transfer to cGMP compliant manufacturing.
  • Oversee, hands-on, critical production activities to ensure appropriate and compliant execution.
  • Interpret, organize and present data to clients and coworkers.
  • This may require 1-2 weekend days/month to support ongoing projects and meet deadlines.


Min:3.0Max:8.0 year(s)

Information Technology/IT

IT Software - Other

Software Engineering


An appropriate area of specialization (molecular biology biochemistry engineering etc



Alachua, FL, USA