Global Lead, IT Compliance and Validation
Global Lead, IT Compliance and Validation

Global Lead, IT Compliance and Validation

Stockton-on-Tees Full-Time 43200 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead a global team in IT compliance and validation, ensuring quality deliverables and collaboration.
  • Company: Join FUJIFILM Diosynth Biotechnologies, a trusted partner transforming lives through innovative solutions.
  • Benefits: Enjoy a hybrid work environment with opportunities for mentorship and professional growth.
  • Why this job: Be part of a fast-growing company that values your potential and encourages you to push boundaries.
  • Qualifications: Bachelor’s degree and 10+ years in computer system validation; strong leadership and communication skills required.
  • Other info: Must reside near Raleigh, NC, Billingham, UK, or Copenhagen, Denmark; U.S. citizenship or eligibility required.

The predicted salary is between 43200 - 72000 £ per year.

The Global leader of IT Compliance & Validation is not directly accountable for a separate budget, but will contribute to the budget process and is responsible for transparency of cost and continuous optimization in their unit. The role includes responsibility for the management and development of the direct reports – in respect to quality of deliverables and cooperation. As a Global Leader you will be responsible for a global team of between 3-8 direct reports – potentially situated across geographic sites. The role includes taking responsibility for delivery and services with impact to business units. Although a hybrid role, the incumbent must reside near one of the following site locations: Raleigh, NC area, Billingham, UK area, Copenhagen, Denmark area You will have the opportunity to work in close relationship with other leaders cross sites and IT functional towers. Principal Accountabilities: Develop global validation team and supporting global processes. Support the organization and computerized system validation team on compliance and regulatory requirements. Mentorship of internal resources. Continuous improvement of CSV delivery methodologies, internal processes and collaboration with ITQ. Develop vendor assurance practice. Verify external CSV resource requirements and deliverables. Coordinate IT audit responses supporting customer and regulatory agency audits and inspections. Background and Education Requirements: Bachelor’s degree in engineering, computer science or similar is required 10+ years industry relevant experience in computer system validation Must also have strong knowledge of documentation standards in particular ISO and cGMP A proven understanding of GAMP A high level of understanding within production and IT Projects Proven team management experience. Ability to lead and develop/mentor a team Excellent communication and interpersonal skills, with the ability to effectively communicate with technical and non-technical stakeholders Desired Experience: Knowledge and experience within the Pharmaceutical industry Overall understanding of the IT strategy and how it supports the business strategy Must be able to present topics with authority to auditors We are a trusted CDMO partner for life. At FUJIFILM Diosynth Biotechnologies (FDB), we encourage you to discover what inspires you every day, to follow your passion and your power – what we call Genki. The work we do has the potential to transform people’s lives and to impact where it matters most. Each day is an opportunity to push the boundaries of your potential, so join our Global IT Team as the Lead for IT Compliance and Validation and become part of a fast-growing global company, united by Genki. As part of any recruitment process, FUJIFILM Diosynth Biotechnologies collects and processes personal data relating to job applicants. The organisation is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations and may share this as part of the global recruitment process with hiring managers in Europe and the United States. FDBU works with technical data, technology and materials that are subject to U.S. export laws and regulations. This position will require access to technical data, technology and source code that is controlled under U.S. export laws and regulations, including but not limited to the International Traffic in Arms Regulations at 22 C.F.R. Parts 120 – 130 and Export Administration Regulations in 15 C.F.R. Part 730 – 774, as may be amended. To conform to these laws and regulations, applicants must be U.S. citizens, lawful permanent residents of the U.S., protected individuals as defined by 8 USC 1324(b)(a)(3) (i.e., asylees and refugees) or otherwise eligible for an export authorization from the U.S. Department of State or U.S. Department of Commerce. Offers of employment will be contingent on the Company’s ability to secure an export authorization. FDBU is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, sexual orientation, gender identify or any other protected class. If an accommodation to the application process is needed, please e-mail FDBUHR@fujifilm.com. To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.

Global Lead, IT Compliance and Validation employer: FUJIFILM Diosynth Biotechnologies

At FUJIFILM Diosynth Biotechnologies, we pride ourselves on being an exceptional employer that fosters a culture of innovation and collaboration. Our Global IT Team thrives in a dynamic environment where mentorship and professional growth are prioritized, allowing you to develop your skills while making a meaningful impact in the pharmaceutical industry. With locations in Raleigh, NC, Billingham, UK, and Copenhagen, Denmark, we offer a hybrid work model that supports work-life balance, ensuring you can pursue your passion and power—what we call Genki—while contributing to life-changing projects.
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Contact Detail:

FUJIFILM Diosynth Biotechnologies Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Global Lead, IT Compliance and Validation

✨Tip Number 1

Make sure to highlight your experience in managing global teams, especially if you've worked with remote teams across different geographic locations. This will show that you can handle the complexities of a global role.

✨Tip Number 2

Familiarize yourself with the latest trends and regulations in IT compliance and validation, particularly in the pharmaceutical industry. Being knowledgeable about ISO, cGMP, and GAMP standards will set you apart.

✨Tip Number 3

Prepare to discuss your mentorship style and how you've developed internal resources in previous roles. This is crucial as the position emphasizes team development and quality deliverables.

✨Tip Number 4

Be ready to demonstrate your communication skills by providing examples of how you've effectively communicated with both technical and non-technical stakeholders. This is key for a leadership role that requires collaboration across various teams.

We think you need these skills to ace Global Lead, IT Compliance and Validation

Leadership Skills
Team Management
Computer System Validation (CSV)
Regulatory Compliance Knowledge
ISO Documentation Standards
cGMP Knowledge
GAMP Understanding
Project Management
Interpersonal Skills
Communication Skills
Continuous Improvement Methodologies
Vendor Assurance Practices
Audit Coordination
Technical and Non-Technical Stakeholder Engagement
Problem-Solving Skills
Adaptability

Some tips for your application 🫡

Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Global Lead, IT Compliance and Validation position. Tailor your application to highlight your relevant experience in compliance, validation, and team management.

Highlight Relevant Experience: In your CV and cover letter, emphasize your 10+ years of industry-relevant experience, particularly in computer system validation and the pharmaceutical industry. Provide specific examples of how you've led teams and managed projects successfully.

Showcase Communication Skills: Since the role requires excellent communication with both technical and non-technical stakeholders, include examples in your application that demonstrate your ability to convey complex information clearly and effectively.

Tailor Your Documents: Customize your CV and cover letter for this specific role. Use keywords from the job description, such as 'GAMP', 'ISO', and 'cGMP', to ensure your application stands out and aligns with what the company is looking for.

How to prepare for a job interview at FUJIFILM Diosynth Biotechnologies

✨Showcase Your Leadership Skills

As a Global Leader, it's crucial to demonstrate your ability to manage and develop a team. Prepare examples of how you've successfully led teams in the past, focusing on mentorship and collaboration.

✨Understand Compliance Standards

Familiarize yourself with ISO, cGMP, and GAMP standards. Be ready to discuss how you have applied these standards in previous roles, especially in relation to computer system validation.

✨Communicate Effectively

You will need to interact with both technical and non-technical stakeholders. Practice explaining complex topics in simple terms, and be prepared to present your ideas confidently.

✨Demonstrate Continuous Improvement Mindset

Highlight your experience with process optimization and continuous improvement methodologies. Share specific examples of how you've enhanced delivery methodologies or internal processes in your previous roles.

Global Lead, IT Compliance and Validation
FUJIFILM Diosynth Biotechnologies
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