Associate Scientist

2 days ago

Thousand Oaks, United States Aequor Full time

Job Title: Associate Scientist

Location: Thousand Oaks, CA – 100% Onsite

Duration: 12 Months with possible extension

Terms: Contract W2


Responsibilities include:

• Participate in the planning, design, execution, and documentation of studies related to drug product formulation and process development by:

- Supporting and executing formulation assessments by utilizing high-throughput technologies and workflows, working closely with program teams on fast-paced projects.

- Supporting studies on advancing automation technologies regarding liquid handling robots, plate-based buffer exchange systems, and high throughput protein characterization assays.

• Evaluate product and process performance through analytical testing (e.g., U/HPLC, CEX, particle analysis, physical properties, etc.) and perform subsequent data analysis and method compliance assessments as appropriate.

• Identify and implement innovative solutions by applying basic science/engineering skills to increase throughput, improve quality, and streamline data capture and analysis.

• Effectively communicate and closely collaborate with the colleagues in the automation team to coordinate, organize and execute studies

• Participate in team meetings by sharing study designs, results, and technical challenges.

• Author and review technical documents, such as technical presentations, protocols, and reports, while ensuring a high standard of data accuracy and integrity

Preferred Qualifications:

• Degree in Chemical Engineering, Biomedical Engineering, Biochemistry, Biotechnology, Pharmaceutics, or related subject area.

• Prior knowledge or industry experience (2+ years) of pharmaceutical/biotechnology process development, protein handling, and processing with a focus in formulation development

• Hands-on experience in executing protein characterization techniques, i.e. SEC-UHPLC, CEX-UHPLC, concentration measurement via UV-Vis, pH, viscosity and other analytical testing.

• Hands-on experience in designing and executing automation and high throughput screening studies on liquid handling platforms (e.g. Tecan, Hamilton, Andrew Alliance, Unchained Labs, etc.)

• Critical thinking, problem solving and independent research skills

• Good organizational skills with strong attention to detail

• Ability to elevate relevant issues to project lead and line-management

• Self motivation, adaptability and a positive attitude with enthusiasm to learn new techniques

• Ability to work independently and as part of a team with internal and external partners

• Ability to participate and work effectively in a fast-paced, dynamic and highly matrixed team environment

• Good organizational skills with strong attention to detail.

• Excellent communication (oral and written).

Basic Qualifications:

• B.S. with 2-5 year experience, M.S. with 0-3 year experience, with degree in Engineering, Chemistry, Biology, Pharmaceutical Sciences, Life Sciences, or related degree with a biotechnology, pharmaceutical or vaccine background. Biotech/pharmaceutical industry experience

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