Hiring: Director Analytical Research & Development - CDMO Company: Randstad USA Location: High Point, NC Job Posted Time: 2026-09-03 14:41:45 Employment Type: Contract Target Skills & Keywords : R, Regulatory Compliance About the job Experience: •10+ years, M.S. with 15+ years, or B.S. with 20+ years of pharmaceutical chemical process development experience. Required Skills: •Direct and mentor Analytical Associate Directors and scientific staff, managing departmental resources, project workflows, and site execution timelines. •Serve as the primary technical client liaison and subject matter expert for small-molecule API analytical development. •Oversee analytical project quoting, budgeting, invoicing, contract discussions, and resource reconciliation. •Ensure strict adherence to global regulatory guidelines (FDA, ICH, USP, EP, JP) and cGMP standards. •Partner with executive site leadership across Chemical Development and Quality to guide long-range business planning and site strategy. Qualifications: •Ph.D. with 10+ years, M.S. with 15+ years, or B.S. with 20+ years of pharmaceutical chemical process development experience. •Proven leadership and direct management experience in a cGMP pharmaceutical R&D or manufacturing setting. •Deep expertise in small-molecule analytical techniques (HPLC, GC, LC/GC-MS, IR) and handling Out-of-Specification (OOS) investigations. •Advanced knowledge of compendial methods, SOP development, and regulatory compliance. Compensation: •$178,000 - $200,000 / year Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!