Process Development Associate: Oral Solid Formulation

Collabera; Thousand Oaks (CA); On-site; USD 34,000 - 36,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) retirement plan

Life insurance

Long-term disability insurance

Short-term disability insurance

Paid parking/public transportation

Paid time off

Paid sick time

Paid vacation time

Paid parental leave

Paid holidays annually

any additional benefits applicable

Job summary

Collabera is seeking a Process Development Associate at our Thousand Oaks, CA headquarters. You will join the Pre-Pivotal Drug Product Technologies organization and work on oral solid dosage form development for early-stage clinical studies.

You will execute formulation experiments, support digital platform initiatives, and document results for cross-functional teams in a GMP/SOP-driven environment.

Qualifications

• Hands-on formulation laboratory experience in oral solid dosage form development.
• Experience with unit operations such as granulation, blending, tablet compression, and film coating.
• Experience with material characterization techniques such as DSC and XRPD; solid dosage form characterization (friability, disintegration, dissolution, density, flowability).
• Understanding of solubility enabling formulations, including amorphous solid dispersions (ASDs) and lipid-based formulations.
• Ability to independently execute experiments, analyze data, document results, and communicate findings to cross-functional stakeholders.

Responsibilities

• Execute small molecule formulation experiments to support development of oral solid dosage forms for early-stage clinical studies.
• Contribute to creation and optimization of digital platform capabilities while supporting experimental efforts to design and optimize drug product formulations and processes.
• Communicate findings clearly to technical and cross-functional stakeholders.

Job description

Collabera is seeking a Process Development Associate at our Thousand Oaks, CA headquarters. You will join the Pre-Pivotal Drug Product Technologies organization and work on oral solid dosage form development for early-stage clinical studies.

You will execute formulation experiments, support digital platform initiatives, and document results for cross-functional teams in a GMP/SOP-driven environment.