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.
- Perform
laboratory-scale purification experiments and analyze experimental data.
- 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.
- Provide
technical support for manufacturing investigations and atypical events.
- Support
purification platform development and evaluation of new technologies.
- Mentor
junior team members on purification strategies, experimental design, and
process transfer.
- Collaborate
cross-functionally with Process Development, Manufacturing, Quality, and
external partners.
- Maintain
laboratory operations, equipment, compliance, safety, and data integrity
standards.
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
- JMP
and/or Spotfire
- Laboratory
automation and data-management tools
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
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.








