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Senior Data Controller - Job Opportunity at Teva Pharmaceuticals

Runcorn, United Kingdom
Full-time
Senior
Posted: May 25, 2025
On-site
£45,000 - £65,000 per year based on senior-level pharmaceutical data management roles in the Runcorn area, with potential for performance bonuses and comprehensive benefits packages typical of multinational pharmaceutical companies

Benefits

Access to comprehensive healthcare benefits as part of a global pharmaceutical leader
Professional development opportunities within a company serving 200+ million patients daily
International career mobility across nearly 60 countries
Exposure to World Health Organization Essential Medicines List production processes
Opportunity to contribute to affordable healthcare accessibility mission

Key Responsibilities

Drive strategic master data governance across manufacturing operations to ensure optimal product flow and accurate financial costing that directly impacts business profitability
Lead cross-functional stakeholder coordination with Manufacturing Science & Technology, Supply Chain, Quality Control & Services, Regulatory Affairs, and Operations to maintain data integrity standards
Provide critical data analysis and oversight that supports executive decision-making for costing reviews and financial planning across all SKUs
Execute workflow management for master data creation and maintenance in MDG systems, ensuring operational continuity and compliance
Establish and monitor key performance indicators for master data maintenance, driving continuous improvement initiatives
Identify and resolve data gaps through proactive risk management, ensuring regulatory compliance and operational accuracy
Manage complex master data requirements for manufacturing, filling, and packing operations within MES/SAP systems
Coordinate master data alignment with new product introduction timelines, supporting business growth and market expansion strategies

Requirements

Education

Relevant degree or extensive experience in a similar role

Experience

Extensive experience in a similar role

Required Skills

SAP systems including SAP Enterprise master data (MDG) SAP S4 HANA ABAP report writing Quality systems, Regulatory process, Glorya, Trackwise and other local processes Work to tight timescales, balance priorities Analytical skills and problem solving Use of analytical tools (such as but not exclusively) – Excel, BI data warehouse Good attention to detail Ability to manipulate data Flexible with respect to work load and responding to various demands Ensure compliance of data at all times
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Sauge AI Market Intelligence

Industry Trends

The pharmaceutical industry is experiencing unprecedented digital transformation, with master data management becoming critical for regulatory compliance under evolving FDA and EMA guidelines. Companies are investing heavily in SAP S/4HANA migrations to improve data integrity and real-time analytics capabilities. Generic pharmaceutical manufacturers are facing increased pressure to optimize operational efficiency while maintaining strict quality standards, making master data controllers essential for cost management and regulatory compliance in an increasingly competitive market. The integration of artificial intelligence and machine learning in pharmaceutical manufacturing is creating new demands for clean, structured master data, positioning data controllers as strategic enablers of digital innovation initiatives.

Role Significance

Typically works within a team of 3-8 data management professionals, collaborating across multiple departments and serving as a key liaison between IT, operations, and business stakeholders
This is a senior individual contributor role with significant cross-functional influence and responsibility for critical business systems. The position requires independent decision-making and strategic thinking, with direct impact on manufacturing operations and financial reporting.

Key Projects

SAP S/4HANA implementation and optimization projects for manufacturing operations Master data governance framework development and continuous improvement initiatives New product introduction data setup and validation processes Regulatory compliance audits and data integrity remediation projects Cross-functional process improvement initiatives involving supply chain and quality systems

Success Factors

Deep technical expertise in SAP MDG and S/4HANA systems combined with strong understanding of pharmaceutical manufacturing processes and regulatory requirements Exceptional stakeholder management skills to coordinate across diverse functional areas while maintaining data quality standards under tight deadlines Proactive problem-solving approach with ability to identify and resolve data inconsistencies before they impact operations or compliance Strong analytical mindset with proficiency in data manipulation tools and ability to translate complex technical concepts for business stakeholders

Market Demand

High demand driven by increasing regulatory requirements, digital transformation initiatives, and the critical need for data integrity in pharmaceutical manufacturing operations

Important Skills

Critical Skills

SAP MDG expertise is absolutely essential as this system forms the backbone of all master data operations, with advanced knowledge required for workflow creation and maintenance. This skill directly impacts operational efficiency and regulatory compliance. ABAP report writing capabilities are crucial for customizing data extraction and analysis processes, enabling the role holder to independently develop solutions for complex data requirements and support business intelligence initiatives. Analytical problem-solving skills are fundamental for identifying data inconsistencies, resolving conflicts between systems, and ensuring data integrity across complex pharmaceutical manufacturing processes.

Beneficial Skills

Experience with additional pharmaceutical systems like Glorya and Trackwise enhances ability to integrate data across quality and regulatory platforms Advanced Excel and BI tools proficiency enables sophisticated data analysis and reporting capabilities that support strategic decision-making Understanding of regulatory compliance frameworks provides context for data governance decisions and supports audit readiness

Unique Aspects

Direct involvement in manufacturing operations that impact millions of patients worldwide through essential medicine production
Exposure to complex international regulatory environments and multi-site data coordination across Teva's global network
Opportunity to work with cutting-edge SAP technologies in a highly regulated industry setting
Role combines technical expertise with business impact, offering visibility into pharmaceutical manufacturing operations and strategic decision-making

Career Growth

Progression to management roles typically occurs within 3-5 years, with opportunities for regional or global responsibilities within Teva's extensive international network

Potential Next Roles

Master Data Manager overseeing multiple sites or regions Data Governance Lead with enterprise-wide responsibilities Manufacturing Systems Manager combining data and process expertise Business Systems Analyst focusing on digital transformation initiatives

Company Overview

Teva Pharmaceuticals

Teva Pharmaceuticals is the world's leading manufacturer of generic medicines and a significant player in specialty pharmaceuticals, serving over 200 million patients daily across nearly 60 countries. The company plays a crucial role in global healthcare accessibility by producing many medicines on the WHO Essential Medicines List.

As a Fortune 500 company and global pharmaceutical leader, Teva offers exceptional stability and career growth opportunities, with strong market position in generic drugs and growing presence in specialty therapeutics
The Runcorn facility represents a key UK manufacturing hub for Teva's European operations, providing exposure to international supply chain management and regulatory compliance across multiple markets
Teva emphasizes mission-driven work focused on improving global health accessibility, fostering a collaborative environment that values diversity and inclusion while maintaining high standards for quality and compliance
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