Associate Scientist - Purification Process Development

Posted One Month Ago
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Oceanside, CA, USA
In-Office
45-45 Hourly
Mid level
HR Tech • Information Technology • Professional Services • Consulting
The Role
Support purification process development, characterization, scale-up, and GMP technology transfer for biologics. Execute lab-scale purification experiments, analyze data, document protocols and ELNs, support manufacturing investigations, mentor junior staff, and collaborate cross-functionally to implement purification platforms and new technologies.
Summary Generated by Built In

Our client, a world leader in biotechnology and gene therapy, is looking for an Associate Scientist, Purification Process Development based in Oceanside, CA.

 

Job Duration: Long Term Contract (Possibility Of Extension)

Pay Rate : $45/hr on W2

 

Company Benefits: Medical, Paid Sick leave, 401K

 

Seeking an Associate Scientist to support purification process development, characterization, scale-up, and technology transfer for biologics in pivotal and commercial development. The role involves hands-on laboratory work, process optimization, GMP manufacturing support, and collaboration with internal and external partners.

 

Key Responsibilities

  • Design and execute purification process development and characterization studies.
  • Support process scale-up, technology transfer, and implementation at internal and external GMP manufacturing facilities.
  • Develop and document experimental protocols, reports, and electronic laboratory records.

Required Qualifications

  • MS + 2 years or BS + 4 years of relevant experience in Chemical Engineering, Biochemistry, Bioengineering, or related discipline.
  • Strong hands-on experience with biologics purification process development.

 

Preferred Technical Skills

  • Chromatography and AKTA/UNICORN
  • Tangential Flow Filtration (TFF), Normal Flow Filtration (NFF)
  • Centrifugation, High-throughput purification screening, Virus inactivation/removal
  • Process scale-up and GMP technology transfer
  • Design of Experiments (DoE), statistics, and data analysis

 

If interested, please share your updated resume at [email protected]/[email protected]



Skills Required

  • MS + 2 years or BS + 4 years in Chemical Engineering, Biochemistry, Bioengineering, or related discipline
  • Hands-on experience with biologics purification process development
  • Support for process scale-up, technology transfer, and GMP manufacturing
  • Develop and document experimental protocols and electronic laboratory records
  • Chromatography experience (AKTA/UNICORN)
  • Tangential Flow Filtration (TFF)
  • Normal Flow Filtration (NFF)
  • Centrifugation
  • High-throughput purification screening
  • Virus inactivation/removal experience
  • Design of Experiments (DoE), statistics, and data analysis
  • Experience with JMP and/or Spotfire
  • Laboratory automation and data-management tools
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The Company
HQ: Newark, CA
Year Founded: 2009

What We Do

Dawar Consulting Inc. is a professional services and staff augmentation firm specializing in IT consulting, workforce solutions, and HCM/HRIS services. They provide technology and business consulting, project delivery, and IT support to help clients achieve their strategic goals. With expertise across IT, Engineering, and Finance, they deliver best-in-class workforce solutions and innovative strategies to drive operational efficiency and business success.

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