At a Glance
- Tasks: Lead a global team in IT compliance and validation, ensuring quality deliverables.
- 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 collaboration.
- Qualifications: Bachelor’s degree and 10+ years in computer system validation required; strong leadership skills essential.
- Other info: Must reside near Raleigh, NC, Billingham, UK, or Copenhagen, Denmark; U.S. citizenship required.
The predicted salary is between 48000 - 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.
FUJIFILM Diosynth Biotechnologies | Global Lead, IT Compliance and Validation employer: FUJIFILM Diosynth Biotechnologies
Contact Detail:
FUJIFILM Diosynth Biotechnologies Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land FUJIFILM Diosynth Biotechnologies | 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 computer system validation (CSV) and compliance within the pharmaceutical industry. Being knowledgeable about ISO and cGMP 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
Since this role involves communication with both technical and non-technical stakeholders, practice articulating complex IT concepts in simple terms. This skill will be essential during interviews.
We think you need these skills to ace FUJIFILM Diosynth Biotechnologies | Global Lead, IT Compliance and Validation
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description and understand the key responsibilities and qualifications required for the Global Lead, IT Compliance and Validation position. Tailor your application to highlight how your experience aligns with these requirements.
Highlight Relevant Experience: In your CV and cover letter, emphasize your 10+ years of industry-relevant experience in computer system validation, particularly in the pharmaceutical sector. Provide specific examples of your achievements in team management and compliance.
Showcase Leadership Skills: Since this role involves managing a global team, be sure to illustrate your leadership and mentorship capabilities. Discuss any previous experiences where you successfully led teams or projects, focusing on collaboration and communication.
Tailor Your Communication: Given the need to communicate effectively with both technical and non-technical stakeholders, ensure that your application reflects your ability to present complex topics clearly. Use language that demonstrates your understanding of both IT and business strategies.
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 and Validation
Make sure you have a solid grasp of compliance and validation processes, especially in the pharmaceutical industry. Be ready to discuss your experience with ISO and cGMP standards, as well as any relevant projects you've worked on.
✨Communicate Effectively
You will need to communicate with both technical and non-technical stakeholders. Practice explaining complex topics in simple terms, and be prepared to present your ideas confidently during the interview.
✨Demonstrate Continuous Improvement Mindset
Highlight your commitment to continuous improvement in processes and methodologies. Share specific examples of how you've implemented changes that led to better outcomes in previous roles.