CSV Lead

CSV Lead

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

  • Tasks: Lead the Computer System Validation strategy and ensure compliance with industry standards.
  • 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 a growing field.
  • Qualifications: Relevant degree in a scientific or technical discipline; experience in Quality Management Systems preferred.
  • Other info: Opportunity to work from the London office and access comprehensive healthcare and pension plans.

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 the CSV Lead role. Our remote work culture fosters flexibility and collaboration, allowing you to thrive while contributing to groundbreaking advancements in cell and gene therapy. With competitive salaries, regular pay reviews, and access to top-notch home office equipment, we ensure our employees are well-supported, while also offering opportunities for professional growth and engaging social events that strengthen team bonds.
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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 any experience you have with Quality Management Systems (QMS) in pharmaceutical or clinical environments. Be prepared to discuss specific projects where you successfully implemented CSV strategies or managed validation timelines.

✨Tip Number 3

Showcase your ability to communicate complex system behaviors clearly. Prepare examples from your past work where you effectively articulated technical details to non-technical stakeholders, as this skill is crucial for collaboration with IT and Quality teams.

✨Tip Number 4

Demonstrate your eagerness to learn and adapt by discussing any recent training or certifications you've pursued in CSV or related fields. This will reflect your proactive approach to professional development and your readiness to embrace new challenges.

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
Analytical Skills
Communication 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 relevant scientific or technical qualifications. 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 company's mission and values. Mention your eagerness to learn and adapt, as well as your ability to work collaboratively and independently, which are key traits for this position.

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 Yourself 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

The company values candidates who can lead investigations into validation-related non-conformances. Prepare examples from your past experiences where you identified root causes and implemented effective solutions.

✨Highlight Collaboration Experience

Collaboration with IT and Quality teams is crucial for this role. Share specific instances where you successfully worked with cross-functional teams to track progress and ensure compliance with validation activities.

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