Intern, Pharmaceutical Engineering, Drug… at Revolution… · Redwood…

Summary: Revolution Medicines is focused on developing innovative therapies for patients with cancer. The intern will play an important role as engineering support within the Drug Product team, working closely with scientists and process engineers to support clinical-stage and late-stage process developments. Responsibilities: - Support formulation and process development and optimization studies conducted according to the principles of Quality by Design (QbD), using tools such as OFAT (one factor at a time) experiments and DOE (Design of Experiments) - Review protocols, manufacturing batch records, and development, campaign, and technical reports for clinical-stage and late-stage manufacturing - Analyze data and perform statistical analysis to support process development and optimization, process capability, and process range justification - Build and maintain databases to manage and track experimental data and results for multiple Programs - Conduct literature reviews and stay updated on the latest advancements in drug product development and manufacturing Required Qualifications: - Working towards a BS or MS or Ph. D in Chemical Engineering, Pharmaceutical Sciences, or related discipline - Strong problem-solving skills with sound technically driven decision-making ability - Effective written and verbal communication skills and interpersonal skills - Ability to review and interpret technical documents and protocols - Strong organizational skills and attention to detail - Ability to work collaboratively in a team environment Preferred Qualifications: - Familiarity with regulatory requirements and guidelines in the pharmaceutical industry - Knowledge of Quality by Design (QbD) principles and tools such as OFAT and DOE a plus - Proficiency in statistical analysis software (JMP) a plus Required Skills: Chemical Engineering, Pharmaceutical Sciences, Quality by Design (QbD), One Factor At a Time (OFAT) experiments, Design of Experiments (DOE), Statistical analysis, JMP software, Regulatory requirements in pharmaceutical industry, Technical document review, Effective written communication, Effective verbal communication Benefits: Competitive cash compensation, Robust equity awards, Strong benefits, Significant learning and development opportunities