Regional Serialization Lead

Job Posted 2 Days Ago Posted 2 Days Ago
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Hiring Remotely in United Kingdom
Remote
Senior level
Biotech
Our Mission is to enable our customers to make the world healthier, cleaner and safer.
The Role
The Regional Serialization Lead will manage serialization responsibilities for the European region, supporting the Serialization Roadmap and ensuring system performance. The role involves collaborating with global and regional sites on compliance, conducting audits, leading system maintenance, and facilitating process improvements while keeping stakeholders informed.
Summary Generated by Built In

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Summary:

Manage the Serialization responsibilities in the European region working closely with the Global System Owner, Business Owner and Regional Packaging Sites. Support and deliver the Serialization Roadmap through governance, addressing the impact of changes and delivering through change control. Ensure optimal system performance and provide exceptional support to sites. Communicate frequently with sponsors and partners at all levels to provide updates on compliance and serialization.

What You Will Do:

Site Based Activity Support (as needed)

Enter data and configuration into site systems. Assist in equipment installation, qualification, and commissioning.

Systems and Processes

Provide leadership for serialization systems supporting configuration, maintenance and testing, partner with IT in coordination of system updates and collaborate with the Engineering and IT teams to ensure uptime and operability.

Documentation

Define global system use, acquire, document and share knowledge solutions and uthor procedures and training documentation in the Document Management systems.

Compliance - Audits

Ensure solutions align with global regulatory requirements (e.g., EU FMD, US DSCSA), stay up to date on evolving legislation, provide regulatory support, conduct internal evaluations to ensure alignment with all compliance requirements and provide serialization support for external site audits including customer and regulatory agencies. 

Knowledge Building, Sharing and Communication

Develop a deep understanding of the deployed Serialization solution, stay informed about trends, changes and preferred solutions related, rovide relevant and timely information to regional and global sites and facilitate and participate in serialization program meetings

Problem Solving - Improvement

Partner with internal teams, external vendors, and trading partners to resolve serialization issues, facilitate global improvements, assist with developing/implementing site improvements abd support cost conscious upgrades delivering improvements without disruption.

Growth Opportunities

Implement programs to measure serialization performance, address exceptions, and ensure systems are functioning as intended and develop and implement Key Performance Indicators

How Will You Get ThereEducation:

  • B.Sc. in a Technical Proficiency preferred

Experience: Minimum requirements

  • 5 years of pharmaceutical manufacturing and/or packaging experience
  • 5 to 7 years direct serialization experience, preferably including Track & Trace

Preferred competencies

  • Strong critical thinking and problem-solving.
  • Direct-Indirect leadership experience
  • Experienced addressing management and internal customers ensuring desired outcomes
  • Experience with change processes/controls
  • Experience with Computer Systems Validation and Continuous Process Validation
  • Experience in protocol and test script preparation
  • Experience with product labeling, bar code standards and grading
  • Experience with vendor management, including selection & qualification
  • Proficient Project Management capabilities.
  • Ability to balance multiple priorities
  • Excellent verbal and written communication
  • Ability to interact with people at all levels of the organization
  • Ability to influence internal/external partners
  • Strong organization skills.

Top Skills

Computer Systems Validation
Continuous Process Validation
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The Company
HQ: Waltham, MA
100,000 Employees
Hybrid Workplace

What We Do

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.

Why Work With Us

You will join a company which every colleague has the opportunity to create possibilities, for oneself, for our customers and patients. There is no more exciting place to be than at the forefront of solving problems which help improve lives around the world. As a company, we are committed to supporting your career aspirations and your journey.

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