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Associate Scientist

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: SSi People
Full Time position
Listed on 2026-07-31
Job specializations:
  • Pharmaceutical
    Pharmaceutical Manufacturing, Pharmaceutical Science/ Research, Validation Engineer, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 85000 - 110000 USD Yearly USD 85000.00 110000.00 YEAR
Job Description & How to Apply Below

Job Title: Associate Scientist

Location: Thousand Oaks, California (On-Site)

Job Summary: We are seeking an Associate Scientist to support technical transfer and lifecycle management activities for commercial drug product fill-finish processes. Our team is looking for a candidate who can combine hands‑on laboratory work with clear, scientifically rigorous documentation to help move projects forward across development and manufacturing.

Responsibilities
  • Author, update, data-verify, and review technical transfer documents, protocols, reports, product impact assessments, and regulatory-support documentation.
  • Compile, analyze, and interpret process development, characterization, validation, and manufacturing data to support technical transfer activities.
  • Support laboratory studies and analytical testing, including formulation, mixing, filtration, sampling, pH, protein concentration, viscosity, and osmolality.
  • Collaborate with cross-functional partners in Manufacturing, Quality, Regulatory, Analytical Sciences, and Engineering to support transfer readiness, troubleshooting, and lifecycle management.
Required
  • Master degree, or Bachelor degree with 2 years of experience, or Associate degree with 6 years of experience, or high school diploma / GED with 8 years of experience.
  • At least 3 years of drug product process development, manufacturing support, or technical transfer experience in the pharmaceutical or biotechnology industry.
  • Hands‑on laboratory and drug product process experience with a strong understanding of formulation, mixing, sterile filtration, filling, and end-to-end fill‑finish processes.
  • Demonstrated ability to author, data-verify, and review technical protocols, reports, impact assessments, transfer documents, and regulatory-support documentation.
About SSI People

With over 26 years of industry experience, SSi People has built its reputation and expertise on putting people first. Everything we do works toward delivering exceptional experience for our consultants, our clients, and our internal team. Through a genuine commitment to people in everything we do. We have developed refined processes and a stellar internal team to deliver talent quickly. More importantly, we focus on building long‑term relationships, not transactions.

Putting people first is just what we do well.

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Position Requirements
10+ Years work experience
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