CSV Lead

CSV Lead

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

  • Tasks: Lead the Computer System Validation strategy for advanced therapy software solutions.
  • Company: Join a pioneering company in cell and gene therapy, making medicine accessible and affordable.
  • Benefits: Enjoy remote work, competitive salaries, top-notch home office equipment, and quarterly social events.
  • Why this job: Be part of a mission-driven team that impacts healthcare while developing your expertise in CSV.
  • Qualifications: Relevant degree in science or tech; experience with QMS in pharma or clinical settings.
  • Other info: Opportunity to work from the London office and access comprehensive healthcare benefits.

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

Blackfield Associates have collaborated with the lead developer of critical manufacturing management systems for advanced therapies in search for a full time remote CSV Lead. About the company: Our client company is founded by Cell and Gene Therapy (CGT) This company is creating a portfolio of software solutions such as electronic Batch Manufacturing Records (eBMR) They provide cell and gene therapy manufacturers with methods to scale their operations Their mission is to make medicine deliverable, available, and affordable. Responsibilities include: Develop, implement, and oversee the risk-based Computer System Validation (CSV) strategy for deploying the company’s main paper-based computer system Provide expert guidance to ensure business compliance with CSV standards, 21 CFR Part 11, and Eudralex Annex 11 regulatory requirements. Prepare documentation in alignment with the V-Model approach outlined in GAMP 5. Serve as a subject matter expert (SME) in CSV and data integrity for client projects, managing associated budgets effectively. Create, review, and execute validation lifecycle deliverables following the V-Model within GAMP 5 and GxP Good Practices. Lead investigations into validation-related non-conformances to identify and address root causes. Assist the project management team in maintaining and managing validation timelines. Advise on GxP compliance and industry best practices. Collaborate with stakeholders, including IT and Quality teams, to track progress and ensure successful completion of validation activities. Desired criteria: Hold a relevant degree in a scientific or technical discipline. Demonstrate the ability to clearly and concisely articulate system integrations. Possess experience with Quality Management Systems (QMS) in pharmaceutical and/or clinical environments. Exhibit a strong eagerness to learn continuously and embraces knowledge beyond a single area of expertise. Effectively explain and communicate complex system behaviours with clarity and precision. Excel in both collaborative team settings and independent work, maintaining strong organisational skills and self-motivation. Additional benefits: Join quarterly social events, whether it’s team-building exercises, dinners, or simply unwinding with a drink or two. Benefit from market-competitive salaries with regular pay reviews to recognize and reward great work. Receive top-of-the-line equipment for your home office setup to maximise productivity. If desired, able to utilise the London office near Oxford street Access to BUPA healthcare Pension matched to 3% and then an increase to 5% after probation completion Life insurance

CSV Lead employer: Blackfield Associates

At Blackfield Associates, we pride ourselves on being an exceptional employer, particularly for our remote CSV Lead role. Our commitment to employee growth is evident through regular pay reviews and access to top-tier equipment for your home office, ensuring you can perform at your best. With a vibrant work culture that includes quarterly social events and the option to utilize our London office, we foster collaboration and community while driving innovation in the cell and gene therapy sector.
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Contact Detail:

Blackfield Associates Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land CSV Lead

✨Tip Number 1

Familiarize yourself with the latest regulations and standards related to Computer System Validation (CSV), especially 21 CFR Part 11 and Eudralex Annex 11. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance and industry best practices.

✨Tip Number 2

Highlight your experience with Quality Management Systems (QMS) in pharmaceutical or clinical environments during networking opportunities. Engaging with professionals in these fields can lead to valuable connections and insights that may help you land the CSV Lead position.

✨Tip Number 3

Prepare to discuss specific examples of how you've managed validation lifecycle deliverables and addressed non-conformances in past roles. Being able to articulate these experiences clearly will showcase your expertise and problem-solving skills.

✨Tip Number 4

Emphasize your eagerness to learn and adapt in your conversations with potential employers. The ability to embrace knowledge beyond a single area of expertise is highly valued, especially in a rapidly evolving field like cell and gene therapy.

We think you need these skills to ace CSV Lead

Computer System Validation (CSV)
Risk Management
Regulatory Compliance (21 CFR Part 11, Eudralex Annex 11)
GAMP 5
Validation Lifecycle Management
Data Integrity
Quality Management Systems (QMS)
Project Management
Root Cause Analysis
Stakeholder Collaboration
Technical Documentation
Communication Skills
Analytical Skills
Organizational Skills
Self-Motivation

Some tips for your application 🫡

Understand the Role: Make sure to thoroughly read the job description for the CSV Lead position. Understand the responsibilities and desired criteria, so you can tailor your application to highlight relevant experiences.

Highlight Relevant Experience: In your CV and cover letter, emphasize your experience with Computer System Validation (CSV), Quality Management Systems (QMS), and any regulatory compliance knowledge you possess. Use specific examples to demonstrate your expertise.

Showcase Communication Skills: Since the role requires clear articulation of complex system behaviors, include examples in your application that showcase your ability to communicate effectively, both in writing and verbally.

Tailor Your Documents: Customize your CV and cover letter to reflect the language and key terms used in the job description. This will help your application stand out and show that you are a good fit for the company’s culture and mission.

How to prepare for a job interview at Blackfield Associates

✨Understand CSV Standards

Make sure you have a solid grasp of Computer System Validation (CSV) standards, especially 21 CFR Part 11 and Eudralex Annex 11. Be prepared to discuss how these regulations impact the deployment of software solutions in the pharmaceutical industry.

✨Familiarize with GAMP 5

Since the role involves preparing documentation aligned with the V-Model approach outlined in GAMP 5, review this framework thoroughly. Be ready to explain how you would apply it in real-world scenarios during your interview.

✨Showcase Your Problem-Solving Skills

Prepare examples of past experiences where you led investigations into validation-related non-conformances. Highlight your ability to identify root causes and implement effective solutions, as this will demonstrate your expertise and proactive approach.

✨Communicate Clearly

As the role requires explaining complex system behaviors, practice articulating technical concepts in a clear and concise manner. This will help you convey your knowledge effectively and show that you can communicate well with both technical and non-technical stakeholders.

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