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Director, Digital and Business Excellence - North America Sterile
Greenville, North Carolina, USA
·
On-site
·
Full-time
·
1mo ago
必須スキル
Lean methodologies
Six Sigma
Strategy deployment
Value stream mapping
Kaizen
Standard work
A3 problem solving
Program management
Financial Analysis
Benefits realization
Change Management
Data Analysis
Statistical tools
Communication
Coaching
Sterile manufacturing
Aseptic fill-finish operations
GxP compliance
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Position Summary:
The Director, PPI Business System – North America Sterile is accountable for end-to-end deployment and execution of the PPI business system across the NA Sterile network (GVL core, with scope expansion to RDG and PLN), delivering measurable improvements in throughput, OEE, right-first-time, deviation reduction, cycle time, service level, and COGS. The role translates operational and compliance challenges into a prioritized portfolio of PPI and digital initiatives, leads cross-functional multi-site execution from opportunity framing through sustained adoption, and ensures Finance-verified benefits aligned with site AOPs and NA Sterile savings targets.
Given the complexity of sterile manufacturing, this role requires deep technical understanding of sterile fill-finish operations to identify root causes, challenge standards, and drive practical, compliant improvements on sterile lines.
Key Responsibilities:
1.
NA Sterile PPI & Digital Program Delivery:
-
Lead the full lifecycle of network PPI and digital initiatives (charter → design → implementation → sustainment), ensuring on-time, on-budget delivery with verified impact.
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Translate NA Sterile priorities into clear charters, scope, milestones, resource plans, and success criteria using PPI standards and divisional templates.
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Own the integrated program plan, dependency management, and RAID discipline; escalate risks/issues with mitigation options and clear decision asks.
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Coordinate site teams and enabling functions (Operations, Quality, Tech Transfer, Engineering, Supply Chain, IT, etc) to deliver compliant and scalable outcomes.
2.
NA Sterile Roadmap & Portfolio Management:
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Build and maintain a prioritized, value-based pipeline aligned with NA Sterile strategy, PPI savings targets, and divisional standards.
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Define annual and multi-year plans: sequencing, capacity needs, key milestones, and readiness requirements (people/process/data/validation).
-
Provide leadership with clear visibility on constraints, trade-offs, and dependencies to enable realistic commitments and fast decisions.
3.
Business Case & Benefits Realization:
-
Co-develop business cases with site leaders, process owners, and Finance; define assumptions, value drivers, measurement methods, and accountable benefit owners.
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Establish a benefits cadence (monthly) and ensure baseline, go-live, stabilization, and run-rate benefits are documented and Finance-validated.
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Ensure accurate input to divisional dashboards and governance reviews, with a single source of truth for KPIs and benefits.
4.
Sterile Line Technical Excellence & Problem Solving:
-
Provide hands-on technical leadership to identify and remove constraints on sterile lines (e.g., line performance losses, aseptic interventions, contamination risks, batch release delays).
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Drive root-cause problem solving using A3, data analysis, and structured experimentation while ensuring compliance with GxP and site procedures.
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Translate sterile technical opportunities into scalable standards (standard work, centerlines, critical parameter management) embedded into daily management.
5. Change Management, Adoption & Standard Work
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Lead change management: stakeholder mapping, communication plans, training strategy, and adoption KPIs.
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Ensure SOP/WI updates, training completion, and readiness checks are in place prior to go-live; treat adoption as a delivery milestone.
-
Embed improvements and digital solutions into tier routines, visual management, leader standard work, and accountability mechanisms to prevent “one-off” gains.
6. Governance, Compliance, Data & Standards
-
Apply the DPD PPI & Digital governance model, delivery gates, and documentation standards, ensuring audit readiness.
-
Ensure compliance with GxP, data integrity, cybersecurity, privacy, and EHS, partnering with Quality/Validation and Cybersecurity to define and execute required validation activities.
-
Confirm data readiness and KPI definitions, partnering with IT/OT and Data & Analytics to maintain consistent definitions and basic governance controls.
Qualifications & Requirements:
Education & Experience
-
Advanced degree + 6 years, or Bachelor’s + 8 years leading Continuous Improvement/Lean business systems across end-to-end value streams; multi-site leadership preferred.
-
Preferred fields: Engineering, Science, Operations, or related.
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Six Sigma Black Belt (or equivalent) required.
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Demonstrated success delivering year-over-year measurable results in productivity, quality, and cost in regulated manufacturing.
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Strong sterile manufacturing domain expertise required (aseptic fill-finish operations, sterile processing, contamination control, line performance drivers, deviation/CAPA, change control, batch release constraints).
Technical & Functional Skills
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Expert knowledge of Lean/PPI: strategy deployment, VSM, kaizen, standard work, A3 problem solving.
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Strong business/financial acumen: productivity funnel management and benefits realization with Finance.
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Strong program management: planning, dependency/RAID management, governance cadence, and stakeholder alignment.
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Digital enablement leadership is a plus: ability to build a prioritized digital pipeline and partner effectively with IT/OT, data engineering/analytics teams, Quality/Validation, and process owners in a regulated environment.
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Data-driven decision making; comfort with statistical tools and CI software.
Leadership & Behavioral Competencies
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Trusted leader able to influence across functions and levels; strong communication and executive presence.
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Strong coaching capability and ability to build CI and digital execution muscle in a matrix environment.
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High standards on safety, quality, compliance, and disciplined execution.
Travel
- Ability to travel up to 50% across the NA Sterile network.
総閲覧数
1
応募クリック数
0
模擬応募者数
0
スクラップ
0
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Thermo Fisherについて

Thermo Fisher
PublicThermo Fisher Scientific Inc. is an American life science and clinical research company. It is a global supplier of analytical instruments, clinical development solutions, specialty diagnostics, laboratory, pharmaceutical and biotechnology services.
10,001+
従業員数
Waltham
本社所在地
$200B
企業価値
レビュー
3.0
10件のレビュー
ワークライフバランス
3.5
報酬
3.8
企業文化
3.2
キャリア
3.5
経営陣
2.1
45%
友人に勧める
良い点
Good benefits and compensation
Nice people to work with
Learning opportunities and skill development
改善点
Poor management and leadership issues
Disengaged or unsupportive management
Frequent reorganizations and chaos
給与レンジ
2,092件のデータ
Junior/L3
Mid/L4
Senior/L5
Junior/L3 · CLIENT SERVICES PROJECT MANAGER III
1件のレポート
$79,685
年収総額
基本給
$79,685
ストック
-
ボーナス
-
$79,685
$79,685
面接体験
8件の面接
難易度
3.0
/ 5
期間
14-28週間
内定率
12%
体験
ポジティブ 12%
普通 63%
ネガティブ 25%
面接プロセス
1
Application Review
2
Recruiter Screen
3
Hiring Manager Interview
4
Panel Interview
5
Final Interview
6
Offer
よくある質問
Technical Knowledge
Behavioral/STAR
Past Experience
Culture Fit
Industry Specific
ニュース&話題
Thermo Fisher Scientific launches Applied Biosystems™ PowerFlex™ Thermal Cycler - BioSpectrum India
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News
·
3d ago
Ninety One North America Inc. Makes New Investment in Thermo Fisher Scientific Inc. $TMO - MarketBeat
MarketBeat
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·
3d ago
Ninety One UK Ltd Has $517.14 Million Stock Position in Thermo Fisher Scientific Inc. $TMO - MarketBeat
MarketBeat
News
·
3d ago
Thermo Fisher Scientific Inc. $TMO Stock Holdings Lifted by Ninety One SA Pty Ltd - MarketBeat
MarketBeat
News
·
3d ago