Senior Scientist Associate - U/HPLC

Global Technical Talent, an Inc. 5000 Company

Thousand Oaks (CA)

On-site

USD 41,000 - 47,000

Part time

2 days ago
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Benefits offered by this job

Medical, Vision, and Dental Insurance
401k Retirement Fund

Job summary

Global Technical Talent is seeking a Senior Scientist Associate - U/HPLC to join a contract, 36-month role in Thousand Oaks, CA. The position focuses on formulation and process development within a pharma/biotech environment, including UF/DF, filtration, and stability studies, with emphasis on analytical evaluation and data-driven decision making.

The ideal candidate will have strong U/HPLC experience, UF/DF operations, and lyophilization skills, plus ability to analyze data and generate clear

Qualifications

  • Experience in U/HPLC of various method types.
  • UF/DF setup and operations.
  • Lyophilization expertise.

Responsibilities

  • Plan and design formulation and process development studies.
  • Execute and document lab studies with high accuracy (UF/DF, filtration, freeze-thaw, stability).
  • Evaluate product/process performance via analytical testing (U/HPLC, particle analysis, moisture).
  • Perform data analysis using statistical software (e.g., JMP, SAS).
  • Apply digital tools to automate data structuring, analyze datasets and build visualizations.

Skills

U/HPLC experience
UF/DF setup
Lyophilization

Education

Doctorate degree
MS + 2 years
BS + 4 years

Job description

  • Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
Senior Scientist Associate - U/HPLC

Location: Thousand Oaks, CA

Onsite Flexibility: Onsite

Contract Details
  • Position Type: Contract
  • Contract Duration: 36 months
  • Pay Rate: $30.00–$34.00 / Hour (USD)
  • Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
Job Summary

This role involves participating in formulation and process development within a pharmaceutical/biotechnology environment, applying science and engineering skills to laboratory studies spanning UF/DF, filtration, freeze-thaw, stability, and analytical evaluation of product and process performance.

Key Responsibilities
  • Participate in the planning and design of formulation and process development studies by applying basic science/engineering skills and prior knowledge
  • Participate in the execution and documentation of laboratory studies with a high degree of accuracy (e.g. UF/DF, filtration, freeze-thaw, stability)
  • Evaluate product and process performance through analytical testing (e.g. U/HPLC, particle analysis, moisture content)
  • Perform data analysis using statistical analysis software (e.g. JMP, SAS, etc.)
  • Apply advanced digital tools to automate data structuring, analyze large and diverse datasets and build intuitive visualizations
  • Author/review technical protocols and reports
  • Participate in team meetings by sharing study designs, results and technical challenges
Required Skills
  • Experience in U/HPLC of various method types
  • UF/DF setup and operations
  • Lyophilization
Preferred Skills
  • Familiarity with pharmaceutical/biotechnology process development
  • Knowledge of Drug Product unit operations (i.e., ultrafiltration/diafiltration, filling, filtration, mixing, etc.) and experience with relevant analytical techniques (i.e., SEC, CEX, HIAC, MFI)
  • Understanding of physical/chemical stability of proteins and how process-related stresses impact molecule attributes and product quality; familiarity with ADCs is preferred
  • Proficiency in at least one statistical software package (e.g., SAS, JMP, or Minitab)
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and align with company policies
  • Self-motivation, adaptability, and a positive attitude
  • Critical thinking, problem-solving, and independent research skills
  • Good organizational skills with strong attention to detail
  • Excellent communication (oral and written)
Education Requirements
  • Doctorate degree OR Master's degree and 2 years of experience OR Bachelor's degree and 4 years of experience
  • Degree in Chemical Engineering, Biomedical Engineering, Biochemistry, Biotechnology, Pharmaceutics, or a related field preferred
Required Experience
  • 1 years of experience in pharmaceuticals/biotechnology that includes process characterization, formulation development, equipment design and implementation, and technology transfers
Benefits
  • Medical, Vision, and Dental Insurance Plans
  • 401k Retirement Fund
Important Notes
  • Interview process: Phone interview to begin, with a follow-up panel for qualified candidates
About GTT

GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. We highly value diverse and inclusive workplaces and support Fortune 500 organizations across banking, financial services, technology, life sciences, biotech, utilities, and retail sectors throughout the U.S. and Canada.

Job Number: 26-26-14854

#gttic

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