Project Manager

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Project Manager Regular Full-Time Professional Boulder, CO, US 6 days ago Requisition ID: 1817 Salary Range: $157,227.00 To $178,972.00 Annually Project Manager Regular Full-Time Boulder, CO, US Salary Range: $157,227.00 – $178,972.00 /year EQUAL OPPORTUNITY EMPLOYER Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices. JOB SUMMARY Corden Pharma Colorado, Inc. seeks Project Manager in Boulder, CO to: Review and update standard operating and quality assurance procedures. Monitor performance of quality control systems to ensure effectiveness and efficiency. Analyze quality control test results and provide feedback and interpretation to production management or staff. Develop project plan including resources, timing, milestones, and deliverables for company’s contractual commitments. Track, monitor, and report key performance metrics including expenditures vs. budget. Manage and control multiple projects to meet objectives. Act as a liaison between the company and customer project manager to ensure mutual agreement of contract scope and schedule. Develop and distribute periodic reports on project performance, issues, risks, and schedules of key activities, events, or milestones. Identify, escalates, and facilitate resolution of manufacturing, supply chain, or quality issues that may adversely affect project performance goals. Ensure risk assessments and appropriate risk mitigation plans are established for projects at every phase of the contract. Collaborate with R&D, Quality, and Operations to understand critical quality product requirements. Assist with the preparation of RFPs. JOB REQUIREMENTS Requires a Master's degree in Regulatory Affairs, Quality Assurance Compliance, or related and 3 years of related experience which must include some experience in each of the following skills: Designing and executing synthetic routes for small molecule APIs, including flow chemistry and batch chemistry, with a focus on scale-up from lab to GMP manufacturing. Manage end-to-end tech transfers of drug substance and drug product manufacturing processes, including documentation package preparation, process fit assessments, and site-to-site alignment. Overseeing manufacturing campaigns within GMP environments, including deviation tracking, batch record reconciliation, and ensuring adherence to regulatory and internal quality systems. Setting up and managing stability studies for drug substances/products in accordance with ICH Q1A(R2) including sample pull schedules, data trending, and report generation. Coordinating with analytical teams to ensure analytical methods are fit-for-purpose, validated per ICH Q2(R1) standards, and successfully transferred to internal or external QC labs; and Managing qualified external labs for product release and stability testing while ensuring timely material delivery and risk mitigation in sourcing plans. This posting will expire on July 22, 2026 BENEFITS 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service #J-18808-Ljbffr