
Global Program Management- Operation Excellence
3 days ago
COGS Analysis & Benchmarking:
Conduct detailed COGS breakdowns for biosimilar products (drug substance, drug product, packaging, logistics).
Identify quick wins and long-term structural changes for cost optimization.
Collaborate with Process Development and Manufacturing teams to optimize upstream and downstream processes, identify inefficiencies in the process and recommend cost saving measures
Drive implementation of single-use systems, continuous manufacturing, or other advanced bioprocessing technologies where feasible.
Optimize inventory and production planning to reduce waste and improve efficiency.
Quality & Regulatory:
~ Collaborate with Quality, Regulatory, and Compliance teams to ensure that cost-saving initiatives meet regulatory standards.
Financial Modeling & Reporting:
Perform variance analysis to detect discrepancies and implement corrective actions
Act as the liaison between R&D, Manufacturing, Quality, Procurement, Finance, and Commercial teams for COGS-related initiatives.
Bachelor's or Master's degree in Biotechnology, Biochemistry, Chemical Engineering , or related field.
MBA or specialized certifications in cost management or lean manufacturing preferred.
Experience:
~7–10+ years of experience in biopharmaceutical manufacturing or operations , with at least 3 years focusing on biosimilars.
~ Proven track record of leading successful COGS reduction initiatives.
Deep understanding of biosimilar development, manufacturing processes, and regulatory frameworks.
Financial acumen with experience in cost modeling and analytics.
Excellent communication and stakeholder management skills.
Key Performance Indicators (KPIs):
~% Successful implementation of identified cost-saving projects.
~ Regulatory compliance of implemented initiatives.
~ Competitive compensation and benefits package.
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