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About TSR:

TSR is a relationship-based, customer-focused IT and technical services staffing company.

For over 40 years TSR, Inc. and its wholly owned subsidiary, TSR Consulting Services, have prospered in the Information Technology staffing business, earning the respect of companies both large and small with well refined candidate screening, timely placement, and a real understanding of the right skill sets required by our clients.

Mission & Vision

We do not believe in building a vision around the company but building a company around our vision, which is simply;

Every employee’s voice matters, their effort is appreciated, and their talent is rewarded.

We challenge each employee daily, to raise the bar on how we treat our consultants and candidates. For far too long in this industry, candidates have been ghosted, lied to, or placed at a client and then forgotten about. Each day our staff works tirelessly at qualifying and placing, top talent with our clients, in a compassionate and caring manner.

Not every candidate is a match for the job, but every candidate and consultant will be treated with respect and professionalism.

Research Associate-Scientific

Job Description

  • Location: Seattle, WA
  • Type: Contract
  • Job #73783

Our client, a leading pharmaceutical company, is hiring a Research Associate Scientific on a contract basis.

Work Location

Seattle, WA

Summary

 

Research Associate – Raw Material Performance Testing

Job Description:

The Raw Material Testing group is seeking an enthusiastic Research Associate to act on development and execution of critical raw material performance testing procedures in support of engineered T-cell programs, commercial and clinical manufacturing. This role will require to deliver high quality work and timely output in a cellular therapeutic GMP laboratory environment.

 

Duties and Responsibilities:

• Performs routine cell culture experiments per written procedures, where ability to recognize deviation from accepted practice is required.

• Assists in design and creation of material testing plans, identifying critical process parameter and handling troubleshooting

• Performs data analysis to establish criticality for processes, presents study data and results in team meetings

• Author timely reports detailing experimental work and summarizing results, maintaining electronic laboratory notebooks

• Assists with the revision and creation of process documents, such as SOPs and electronic work instructions

• Collaborate with others to handle day to day operation of the laboratory to ensure smooth operation.

• Maintains laboratory space to comply with regulatory requirements and safe work environment

• Works in teams and has continual interaction with internal as well as external teams throughout the production process in order to exchange information regarding the run(s) in process.

Required Qualifications

• Experience with aseptic processing of mammalian or primary cell culture in biological safety cabinet

• Excellent documentation and data management skills

• Detail oriented with excellent verbal and written communication skills

• Demonstrated proficiency in common computer tools such as word processing, spreadsheet and web-based applications.

• Demonstrated ability to work well both independently and on a team in a fast-paced environment, and prioritize work across multiple projects

 

Preferred Qualifications

• Experience scientific writing and executing process development experimental plans and technical reports

• Experience with JMP or R for statistical analysis, experimental design, and presentation of experimental results

• Experience working in, or exposure to, GMP setting, especially using Good Documentation Practices

 

Education Requirements

• B.S. in Chemical/Biological Engineering, Immunology, Biology or relevant scientific discipline with 0-2 years of biotechnology or cell therapy industry experience

 

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