Strategic Sourcing Manager

Role Description The Owner role at ORDON is a full-time remote leadership position responsible for overseeing strategy, operations, and client engagement for GMP consultation services. Daily activities include defining business goals, developing service offerings, and ensuring that all client projects meet GMP, quality, and regulatory standards. The Owner will lead business development efforts by identifying new opportunities, preparing proposals, and maintaining strong relationships with existing and prospective clients. This role includes managing financial performance, budgeting, and resource allocation, as well as guiding contractors or partner consultants to deliver consistent, high-quality work. The Owner will also represent ORDON in industry forums, maintain awareness of evolving GMP regulations, and drive continuous improvement in internal processes and client solutions.QualificationsExtensive knowledge of GMP regulations and quality systems in human, veterinary, or cosmetics pharmaceuticals, with proven experience in compliance, audits, and regulatory interactions.Strong business leadership and entrepreneurship skills, including strategic planning, financial management, and decision-making in a consulting or service-based environment.Demonstrated client relationship management skills, including needs assessment, solution design, proposal development, and long-term account stewardship.Experience in quality assurance, risk management, and SOP development, including the ability to design, review, and optimize documentation and operational workflows.Ability to design and deliver training, workshops, and educational materials on GMP topics to diverse audiences with varying levels of expertise.Excellent written and verbal communication skills, with the ability to present complex regulatory and technical information clearly and concisely.Proven ability to work independently in a remote setting, prioritize multiple projects, and meet deadlines with minimal supervision.Bachelor’s degree or higher in Pharmacy, Chemistry, Life Sciences, Engineering, or a related field; advanced certifications in quality or regulatory affairs are a plus.Previous experience in consulting, pharmaceutical manufacturing, or regulatory affairs is strongly preferred.