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- Tasks: Lead and supervise validation activities for GMP systems in the pharmaceutical industry.
- Company: Join Almac, a leader in pharmaceutical services with a commitment to excellence.
- Benefits: Enjoy staff discounts, professional coaching, healthcare schemes, and a pension plan.
- Why this job: Be a key player in ensuring compliance and quality in a dynamic industry.
- Qualifications: Degree in relevant field or significant experience in Computerised Systems Validation required.
- Other info: Apply by 8PM on February 4, 2025, and tailor your CV to stand out!
The predicted salary is between 43200 - 72000 £ per year.
Validation Technical Leader (Computerised Systems Validation) Location: Craigavon Hours: 37.5 Salary: Competitive Business Unit Sciences Open To: Internal & External Applicants Ref No.: HRJOB10245/1 Please note this is a re-advertisement, if you have applied for this position recently there is no need to re-apply The Role The primary purpose of this role is to perform, and supervise staff in, activities within the validation lifecycle of all GMP systems requiring validation. Is your CV ready If so, and you are confident this is the role for you, make sure to apply asap. This role is specifically in relation to Computerised Systems Validation (CSV) in accordance with pharmaceutical industry regulations and guidance. Systems will range from standalone equipment to complex multi-site enterprise level systems. The post holder will be a positive role model, demonstrating excellence in technical and practical knowledge, customer care, planning, QA and results delivery. This role assumes an excellent understanding and demonstrated knowledge of CSV within the validation lifecycle. This allows the Technical Leader to not only perform their own activities but also provide advice to others from system selection through to delivery and ongoing compliance. The post-holder will be considered the CSV SME and will be required to attend and present at technical meetings and audits/inspections. Please see attached job description for further details Key Requirements Applicants must have eligibility to work in the UK OR possess a valid work permit that will allow you to take up full time, permanent employment in the UK Essential Criteria Degree (or equivalent) in Analytical Chemistry, Chemistry, Biochemistry, Engineering, IT or a related field OR significant relevant experience may be considered in lieu of Degree Level Qualification Significant Experience in a CSV role within the Pharmaceutical Industry Experience Reviewing and approving cGMP Validation Documentation Understanding of Pharmaceutical Industry Regulations and Guidance related to CSV/DI Please see attached job description for further details of essential and desirable criteria. Apply Now Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible. Closing Date We will no longer be accepting applications after 8PM on Tuesday 04 Feb 2025 RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CVs received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation. Skills: Computer System Validation Validation Quality Compliance GMP Experience Benefits: Staff Discounts Professional Coaching Employee Recognition Rewards for Years Of Service Group Healthcare Scheme Pension Scheme
Validation Technical Leader (Computerised Systems Validation) employer: Almac Group Ltd
Contact Detail:
Almac Group Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Validation Technical Leader (Computerised Systems Validation)
✨Tip Number 1
Familiarize yourself with the latest regulations and guidance related to Computerised Systems Validation (CSV) in the pharmaceutical industry. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in this field.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who specialize in CSV. Attend relevant conferences or webinars to connect with potential colleagues and learn about industry best practices.
✨Tip Number 3
Prepare to discuss specific examples from your past experience where you successfully managed validation processes or overcame challenges in CSV. Being able to articulate these experiences will set you apart as a candidate.
✨Tip Number 4
Showcase your leadership skills by highlighting any experience you have in supervising teams or mentoring others in the validation lifecycle. This is crucial for the Technical Leader role and will demonstrate your readiness for the position.
We think you need these skills to ace Validation Technical Leader (Computerised Systems Validation)
Some tips for your application 🫡
Tailor Your CV: Make sure to customize your CV to highlight your experience in Computerised Systems Validation (CSV) and how it aligns with the requirements of the role. Emphasize your understanding of pharmaceutical industry regulations and any relevant projects you've worked on.
Highlight Relevant Experience: Clearly outline your significant experience in a CSV role within the pharmaceutical industry. Include specific examples of validation documentation you have reviewed and approved, as well as any technical meetings or audits you have participated in.
Use Clear Formatting: Ensure your CV is easy to read by using clear headings, bullet points, and consistent formatting. This will help the hiring team quickly identify your qualifications and experience related to the role.
Submit in PDF Format: When you're ready to apply, upload your CV in PDF format if possible. This ensures that your formatting remains intact and looks professional when viewed by the hiring team.
How to prepare for a job interview at Almac Group Ltd
✨Showcase Your CSV Expertise
Make sure to highlight your experience in Computerised Systems Validation. Be prepared to discuss specific projects you've worked on, the challenges you faced, and how you ensured compliance with pharmaceutical industry regulations.
✨Demonstrate Leadership Skills
As a Validation Technical Leader, you'll need to show that you can lead and supervise others. Share examples of how you've successfully managed teams or projects in the past, focusing on your ability to mentor and guide staff.
✨Prepare for Technical Questions
Expect to be asked technical questions related to GMP systems and validation documentation. Brush up on relevant regulations and guidance, and be ready to explain how you apply this knowledge in practical scenarios.
✨Engage in the Interview
Interviews are a two-way street. Prepare thoughtful questions about the company's approach to validation and how they support their employees' professional development. This shows your interest in the role and helps you assess if it's the right fit for you.
