Process Development Associate

Reference: 630021Posted: 2026-08-11Location: Thousand Oaks, CACompany: Planet Pharma GroupContact: ApplicationsEmail: View email address on click.appcast.io PR Range: 19-25/hr DOEWe are seeking a quicker learner and detail-oriented, team-focused Process Development Associate to support the ATO Rapid Analytics (RA) group within Process Development. In a fast-paced, highly matrixed laboratory environment, this individual will perform product quality analyses and generate high-quality analytical data to meet project timelines and enable process decisions. The role partners closely with scientists and stakeholders across multiple sites and functional areas. Key Responsibilities Analytical Testing * Execute analytical tests within expected turnaround times, following approved methods and data integrity practices, using assays such as: o Compendial testing including pH, visual, color, clarity, Osmolarity, and protein concentrations o Size Exclusion Chromatography (SEC) o Titer o Cation Exchange Chromatography (CEX) o Reduced Capillary Electrophoresis (rCE-SDS) o Non-Reduced Capillary Electrophoresis (nrCE-SDS) o Capillary Ion Electrophoresis Focusing (cIEF) o ATOLL Compliance and Documentation:

• Adhere to turnaround times and required metrics for high throughput samples.
• Document and review results in electronic laboratory notebooks in a timely manner.
• Author, review, and verify technical documents and reports.

Logistics and Planning:

• Manage logistics tasks including sample receiving and equipment maintenance.
• Monitor the safety and compliance status of the ATO RA lab.

Collaboration and Communication:

• Work with the development team to implement methods, analyze data, and interpret results.
• Provide technical input and generate written reports as needed.
• Communicate project updates effectively.
• Present scientific data in meetings.

Maintenance and Troubleshooting:

• Maintain lab instruments and follow equipment cleaning protocols.
• Solve technical problems related to instruments and assays.

Required Qualifications

• Bachelors degree in Chemistry, Biochemistry, Biology, Chemical Engineering, or related discipline (or equivalent combination of education and experience).
• 0-2 years of relevant laboratory experience (industry, academic, or internship).
• Understanding with some hands-on experience with chromatographic and/or electrophoretic techniques is a bonus
• Strong attention to details.
• Ability to follow written procedures, maintain accurate records, and work safely in a laboratory environment.
• Strong organizational skills with the ability to manage multiple priorities and meet timelines.

Preferred Qualifications

• Good understanding of liquid chromatography and capillary electrophoresis, with strong hands-on technical skills to address challenging technical issues.
• Strong ability to analyze and interpret analytical results.
• Excellent organizational and communication (oral and written) skills, with attention to detail.
• Strong interpersonal skills
• Ability to learn new technology quickly, multitask, and adapt in a dynamic environment.
• Possess a positive attitude and strong self-motivation.

Work Environment / Additional Information

• On-site laboratory role; adherence to safety training, PPE, and site procedures is required.
• Work involves handling biological samples and operating analytical instrumentation.
• Documentation is maintained in electronic systems (e.g., electronic laboratory notebook); accuracy and data integrity are essential.
• May require flexibility to support project timelines (e.g., occasional schedule adjustments).