Research Associate II/Senior Research Associate

Posted Yesterday
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Bothell, WA, USA
In-Office
70K-90K Annually
Senior level
Biotech • Pharmaceutical
The Role
Supports downstream protein purification, characterization, and process development for biopharmaceutical molecules. Performs chromatography, tangential flow filtration, viral clearance, filtration, analytical assays, and low-endotoxin production runs. Uses ÄKTA systems and biophysical instruments, analyzes and reports data, authors SOPs, supports tech transfer to GMP manufacturing, and contributes to process scale-up, scale-down, and timeline planning. The role is full-time onsite and may occasionally require work outside normal hours.
Summary Generated by Built In

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. 
 

The Research Associate II/Senior Research Associate will assist in downstream protein purification, protein characterization, and process development. The position will directly report to a Downstream lead and assist in downstream process development and tech transfer to a GMP manufacturing facility. In this role, the individual will assist and operate both routine and advanced analytical instruments as well as protein purification systems. 

This position is full-time onsite at our new Bothell, WA location. This role may occasionally need to work outside normal work hours.
Key Responsibilities:

  • Assist in downstream process development of molecules in pre-clinical and clinical pipelines. Process development activities include buffer preparation, chromatography method development and execution, TFF, and filtration operations and development 
  • Assist in performing routine purifications and analytical assays to support cell-line development, upstream, analytical, and formulation groups 
  • Execute development experiments to produce scalable and robust purification processes via affinity chromatography, IEX, HIC and CHT, etc, using the ÄKTA FPLC platform.  Execute development experiments to produce scalable and robust viral inactivation, viral filtration and tangential flow filtration process 
  • Generate low endotoxin production runs for pre-clinical studies 
  • Perform routine HPLC/UPLC, CE, cIEF, octet, ELISA and other biophysical techniques to support upstream, downstream, and formulation process development 
  • Compile, analyze, and report data for process development, tech transfer documentation, and other internal partners 
  • Author standard operating procedures for biophysical assays and standard workflows 
  • Participate in timeline planning 
  • Other duties as assigned 

Required Skills & Qualifications:  

  • MS or BS in Protein Science, Chemical Engineering, Biochemistry or a related field and relevant pharmaceutical or biotech experience 
  • Research Associate II - requires 2+ years of industry experience 
  • Senior Research Associate - requires BS with 5+ years of experience or MS degree with 3+ years of industry experience 
  • Experience with protein chromatography and filtration methods, and protein analysis techniques 
  • Ability to execute SOPs and biophysical assays, and experiments designed for process development of pipeline molecules independently 
  • Hands-on experience in: 
    • ÄKTA Protein Purification Systems and Unicorn software 
    • SEC-HPLC/UPLC 
    • Purification Process Development   
    • Crossflow and Tangential Flow Filtration techniques   
    • Column packing / unpacking   
    • Viral inactivation and viral filtration process development / Viral clearance study   
    • Low endotoxin production run   
    • Process scale-down/scale-up 


Compensation and Benefits: 

The expected base salary range for this position is $70,000 - $90,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s level qualifications, experience, and skills. 

While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role. 

  

SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE. 

  

We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. 

  

SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply. 

Skills Required

  • MS or BS in Protein Science, Chemical Engineering, Biochemistry, or a related field
  • Relevant pharmaceutical or biotechnology industry experience
  • Research Associate II applicants must have 2 or more years of industry experience
  • Senior Research Associate applicants must have a BS with 5 or more years of experience or an MS with 3 or more years of industry experience
  • Experience with protein chromatography and filtration methods
  • Experience with protein analysis techniques
  • Ability to independently execute SOPs, biophysical assays, and process development experiments
  • Hands-on experience with ÄKTA protein purification systems and Unicorn software
  • Hands-on experience with SEC-HPLC or UPLC
  • Experience in purification process development
  • Experience with crossflow and tangential flow filtration techniques
  • Experience with column packing and unpacking
  • Experience with viral inactivation, viral filtration, or viral clearance studies
  • Experience with low-endotoxin production runs
  • Experience with process scale-down and scale-up
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The Company
HQ: Redmond, Washington
83 Employees
Year Founded: 2014

What We Do

Located in Redmond WA, founded in 2014, Systimmune Inc. is a bio-pharmaceutical company focused on the treatment of cancer through developing novel therapeutic bi-specific, and tri-specific antibodies, as well as antibody-drug conjugates (ADC's). Our objective is to create biologics that work through systematic intervention on the solid tumor micro-environment, to either directly attack the tumor and/or to activate the immune system to attack the tumor. We are a group of highly experienced immuno-oncology scientists utilizing several technology platforms to develop world class advanced antibody-based drug therapies.

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