Senior Director of Program Management, Global Operations

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🕒 June 18

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Logo of JSR Micro, Inc.

JSR Micro, Inc.

51 - 200 employees

🏭 Manufacturing

Semiconductor • Manufacturing • Technology

JSR Micro, Inc. is a leading supplier of high-performance semiconductor lithography materials. With over 30 years of excellence in manufacturing and innovation, JSR Micro focuses on developing advanced electronic materials, particularly for the semiconductor industry. The company recently expanded its capabilities by acquiring Yamanaka Hutech Corp. , a manufacturer of high-purity chemicals for semiconductors, which strengthens its market position and aligns with its growth strategy. JSR Micro is recognized for its commitment to sustainability and quality, as evidenced by its recent awards for outstanding performance in front-end quality.

📋 Description

• provides enterprise-level leadership across KBI’s Program Management Office • overseeing complex, multi-modality programs spanning Drug Substance (BDS), Drug Product (DP), and Fill/Finish partner networks • accountable for program execution and client delivery, as well as PMO strategy, operational excellence, and organizational maturity • serves as a senior client executive partner, ensuring alignment across KBI, clients, and strategic collaborators • manages project timelines through all phases of development, from project award and kick-off through close-out • develops, manages, and updates project plans in a timely manner • communicates project status, progress, timelines, changes in schedule, and technical and/or quality issues • schedules, facilitates and documents program related client team meetings • leads cross-functional teams without direct authority • analyzes risk, establishes contingency plans and identifies trigger events and responsibility for initiating mitigating action.

🎯 Requirements

• Masters of Business Administration (MBA), Masters of Science (M.Sc) or Doctorate (Ph.D.) required • Bachelor’s degree (B.Sc) in science or related discipline with >15 years relevant industry experience accepted in lieu of advanced degree • PMP certification (current or planned in the immediate future) • Minimum 15 years industry experience, with 8 years or more direct project management experience • Prior experience effectively managing projects in pharmaceutical or biotech company, CDMO, CRO or related experience required • Experience with client contract negotiations required • Previous personnel management (>5 years) is essential • Demonstrated experience in building project management tools/templates, improving project systems and implementing best practices • Adaptability and flexibility including the ability to manage deadline pressure, ambiguity and change • Ability to build teams and generate a spirit of collaboration while coordinating diverse activities and groups.

🏖️ Benefits

• annual bonus structure for all employees • medical, dental, and vision coverage • paid PTO and holidays • Sabbatical program • 401K matching with 100% vesting in 60 days • employee recognition programs

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