At a Glance
- Tasks: Lead validation compliance activities and ensure adherence to GMP and GxP standards.
- Company: Join a leading Animal Health Operations team in the UK.
- Benefits: Fixed-term contract until 2027 with competitive salary and professional growth opportunities.
- Other info: Collaborative environment with opportunities for continuous learning and development.
- Why this job: Make a real impact in animal health while ensuring quality and compliance.
- Qualifications: Degree in science or engineering; extensive validation experience required.
The predicted salary is between 50000 - 60000 ÂŁ per year.
We are now hiring a QA Validation Compliance Lead for our Animal Health Operations in the UK. This role is responsible for managing Validation Compliance activities for the Pirbright site, ensuring that all validation processes, documentation and systems meet GMP, GxP and corporate requirements. This is a fixed‑term contract until 31st December 2027.
Tasks & Responsibilities
- Validation Compliance Oversight
- Manage Validation Compliance activities to ensure operational site objectives are met within agreed timelines.
- Exchange knowledge and expertise with cross‑functional teams, ensuring the site is supported by an expert and flexible Validation Compliance function.
- Plan, resource and manage external contractors’ scopes of work, ensuring effective oversight and communication.
- Oversight and approval of validation activities and documentation applicable to the Pirbright site.
- Serve as Compliance and Regulatory Subject Matter Expert for validation and qualification aspects of projects.
- Approve internal procedures and policies related to validation.
- Oversee compliance of validation processes and support the definition of validation strategies.
- Maintain oversight and ownership of Site Validation Master Plans.
- Validation Documentation & Quality Support
- Ensure validation documentation meets corporate procedures, policies and GMP regulations.
- Work closely with the Validation Execution team and other site functions to ensure best practices in validation documentation and generation of protocols and reports.
- Manage compliance‑related project activities, ensuring alignment with regulatory timelines and requirements.
- Conduct periodic reviews of validation systems and ensure validated status is maintained.
- Provide site visibility of validation performance through monthly KPI reporting and annual reviews.
- Audits & Regulatory Support
- Support Quality Management System activities including audits, inspections, CAPAs, Change Controls and Risk Assessments.
- Participate in vendor audits and support corporate Supplier & Service Provider Audits.
- Ensure adherence to BI and regulatory requirements related to validation.
- Provide SME support during external and internal inspections.
- Cross-Functional Collaboration
- Work with colleagues, contractors, suppliers, stakeholders and process owners to understand validation needs and requirements.
- Join cross‑functional development teams for review and approval of modifications to equipment, processes and systems.
- Share expertise to drive continuous improvement and aligned validation practices across the site.
- Industry & Compliance Monitoring
- Investigate trends in validation and regulatory expectations, updating local systems accordingly.
- Perform gap analyses to assess compliance risk and propose improvements.
- Attend seminars and training events to remain up to date with industry expectations and regulatory changes.
Requirements
- Education
- Degree qualified in a related science or engineering discipline, or formal qualification relating to validation or quality.
- Skills & Experience
- Extensive experience in validation roles or other relevant experience.
- Previous experience in a pharmaceutical or GMP‑regulated environment desirable.
- Strong experience with validation and qualification, including Equipment, CSV, Facilities & Utilities, Process Validation and Cleaning Validation.
- Experience in aseptic production and biologics beneficial.
- Strong understanding of current GMPs, validation requirements and risk assessment principles.
- Proven ability to work autonomously and lead within a team environment.
- Strong written and verbal communication skills.
- Excellent organisational skills and attention to detail.
- Strong analytical and problem‑solving abilities.
- Ability to manage time and resources efficiently and adapt to changing priorities.
- Ability to influence and collaborate effectively with other departments.
- Proactive mindset with capability to identify issues and drive appropriate solutions.
- Strong computer literacy (MS Office, Teams, other GxP systems).
A Disclosure and Barring Service (DBS) check will be required for the successful candidate. Any offer of employment will be subject to satisfactory DBS certificate.
QA Validation Compliance Lead employer: Boehringer Ingelheim
Contact Detail:
Boehringer Ingelheim Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA Validation Compliance Lead
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those who work at companies you're interested in. A friendly chat can open doors and give you insider info that could help you stand out.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Tailor your answers to show how your experience aligns with their values and needs. We want to see that you’re not just a fit on paper but also a great match for the team!
✨Tip Number 3
Practice makes perfect! Do mock interviews with friends or use online platforms. The more comfortable you are speaking about your skills and experiences, the more confident you'll be when it counts.
✨Tip Number 4
Don’t forget to follow up after interviews! A quick thank-you email can leave a lasting impression and shows your enthusiasm for the role. Plus, it keeps you on their radar as they make their decision.
We think you need these skills to ace QA Validation Compliance Lead
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the QA Validation Compliance Lead role. Highlight your experience in validation and compliance, especially in GMP-regulated environments. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Share specific examples of your past experiences that relate to the responsibilities listed in the job description.
Showcase Your Attention to Detail: In a role focused on compliance and validation, attention to detail is key. Make sure your application is free from typos and errors. We appreciate candidates who take the time to present their best work!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Boehringer Ingelheim
✨Know Your Validation Stuff
Make sure you brush up on your knowledge of validation processes, GMP, and GxP regulations. Be ready to discuss how you've applied these in previous roles, especially in a pharmaceutical or GMP-regulated environment.
✨Showcase Your Collaboration Skills
This role involves working with cross-functional teams, so be prepared to share examples of how you've successfully collaborated with others. Highlight any experiences where you exchanged knowledge or drove continuous improvement.
✨Prepare for Compliance Questions
Expect questions about compliance-related project activities and how you've managed them. Think of specific instances where you ensured alignment with regulatory timelines and requirements, and be ready to discuss the outcomes.
✨Demonstrate Your Problem-Solving Abilities
Be ready to talk about challenges you've faced in validation roles and how you approached solving them. Use the STAR method (Situation, Task, Action, Result) to structure your answers and show your analytical skills.