Quality Validation Specialist - Projects - 1yr Fixed Term Contract in Hatfield

Quality Validation Specialist - Projects - 1yr Fixed Term Contract in Hatfield

Hatfield Temporary 40000 - 50000 € / year (est.) No home office possible
Eisai

At a Glance

  • Tasks: Provide quality oversight and validation expertise for exciting facility expansion projects.
  • Company: Join Eisai, a leading pharmaceutical company with a patient-first philosophy.
  • Benefits: Competitive salary, electric vehicle charging, onsite perks, and learning opportunities.
  • Other info: Inclusive and collaborative work environment at our EU Headquarters.
  • Why this job: Make a real impact in healthcare while working on innovative projects.
  • Qualifications: Knowledge of quality control systems and validation requirements is essential.

The predicted salary is between 40000 - 50000 € per year.

The Company Eisai is a leading research based pharmaceutical organisation with an extensive portfolio across the Oncology, Neurology and Pain therapy areas. Eisai Manufacturing is the hub of Eisai’s production and supply chain. We make tablets, package these into blisters, label and package vials and bottles. We also manage the wider medicines supply chain and other companies who undertake work on our behalf. By joining Eisai, you will be working for an organisation with a human healthcare philosophy, which means that we put the patient first in everything we do.

Your new role This role is responsible for providing Quality oversight, validation expertise and strategic support for the successful delivery of EML’s facility expansion projects. The role ensures that all qualification and validation activities associated with new facilities, utilities, warehouse operations, and packaging lines are planned and executed in accordance with EML procedures, regulatory expectations, and industry standards. The job holder will support the development and implementation of validation strategies for the new UK cold‑chain warehouse, new vial packaging line, new auto‑injector packaging line, and associated facility and utility upgrades, ensuring compliance with GMP, GDP, Annex 15, GAMP 5, and EMLs procedures. The role will provide Quality review and approval of validation documentation, risk assessments, commissioning and qualification deliverables, and ensure that systems, equipment and facilities are introduced in a compliant and controlled manner. It will also contribute to the creation, review and maintenance of validation‑related policies, procedures and templates to ensure they remain aligned with current regulatory and project requirements. The job holder will act as a Quality Subject Matter Expert (SME) for qualification, validation, and CSV within the scope of the facility expansion projects, ensuring the application of data integrity principles and supporting successful project execution from design through to handover and operational readiness.

What are we looking for?

  • Ability to establish and maintain effective working relationships and communication links within EML, affiliated organisations and other customers
  • Ability to understand and analyse user requirements to facilitate changes and system improvements
  • Proficient knowledge of electronic systems, CSV and GAMP requirements
  • Working knowledge of facility and utility systems such as HVAC, compressed air, environmental monitoring systems
  • Good understanding of the requirements of data integrity and application to system management
  • Good understanding of Quality Control Systems and analytical software and electronic Quality Systems
  • Good technical and scientific judgement
  • Ability to interpret complex data and present key findings
  • Ability to describe technical information in easy-to-understand terms.
  • Computer literate e.g. Word, Excel and PowerPoint
  • Good understanding of GMP Guidelines and Regulations
  • Knowledge of the qualification and validation requirements for equipment and electronic systems
  • Maintain knowledge and understanding of technical advancements in electronic systems

What we offer in return Eisai offers a competitive salary and excellent wider benefits package that includes:

  • Electric charging points for Electric/Hybrid vehicles
  • Discretionary Bonus
  • Free onsite parking
  • Subsidised onsite restaurant and coffee shop
  • Learning and development opportunities
  • Retail discounts
  • Well-being & mental health awareness programmes
  • Multi-faith prayer room

You will also be based out of our excellent EMEA Knowledge Centre (EKC) facility, which is our EU Headquarters, and offers an inclusive, and collaborative working environment.

What you need to do next If you are interested in this position, please click ‘apply now’ at the top of this advert. Upon submitting your application, you will be asked to complete your profile and upload a copy of your CV along with any additional information to support your application. If you have any questions, please contact us on TalentAcquisition@eisai.net

Eisai Recruitment Statement Diverse perspectives and experiences are critical to our success, and we welcome applications from all people from all backgrounds with the experience and skills needed to perform this role. We look forward to receiving your application.

Eisai EMEA EDI Commitment Statement We believe that diverse and inclusive teams promote wellbeing, learning and innovation, helping Eisai serve our patients, their families, our employees, and society. Our commitment is:

  • to embrace and celebrate our differences, respecting and valuing each other.
  • to include equity, diversity, and inclusion practices in all that we do so everyone has a full sense of belonging.
  • to value individual talent where every employee can be themselves and thrive in an environment of openness, trust, and integrity.

Quality Validation Specialist - Projects - 1yr Fixed Term Contract in Hatfield employer: Eisai

Eisai is an exceptional employer that prioritises a human healthcare philosophy, ensuring that patient care is at the forefront of all operations. With a strong commitment to employee well-being, Eisai offers a competitive salary, comprehensive benefits including learning and development opportunities, and a collaborative work environment at the EMEA Knowledge Centre. Employees can thrive in a culture that values diversity, inclusion, and personal growth, making it a rewarding place to build a career in the pharmaceutical industry.

Eisai

Contact Detail:

Eisai Recruiting Team

StudySmarter Expert Advice🤫

We think this is how you could land Quality Validation Specialist - Projects - 1yr Fixed Term Contract in Hatfield

Tip Number 1

Network like a pro! Reach out to current or former employees at Eisai on LinkedIn. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.

Tip Number 2

Prepare for the interview by brushing up on your knowledge of GMP guidelines and validation processes. We want to see that you can talk the talk and walk the walk when it comes to quality oversight.

Tip Number 3

Show off your problem-solving skills! Be ready to discuss how you've tackled challenges in previous roles, especially those related to quality control and compliance. Real-life examples will make you stand out.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re genuinely interested in joining our team at Eisai.

We think you need these skills to ace Quality Validation Specialist - Projects - 1yr Fixed Term Contract in Hatfield

Quality Oversight
Validation Expertise
GMP Compliance
GDP Compliance
Annex 15 Knowledge
GAMP 5 Knowledge
Risk Assessment

Some tips for your application 🫡

Tailor Your CV:Make sure your CV is tailored to the Quality Validation Specialist role. Highlight relevant experience and skills that match the job description, especially around validation expertise and compliance with GMP guidelines.

Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about quality oversight and how your background aligns with Eisai's human healthcare philosophy. Keep it concise but impactful!

Showcase Your Technical Skills:Don’t forget to mention your proficiency in electronic systems and your understanding of GAMP requirements. These are key for the role, so make sure they stand out in your application.

Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets to the right people. Plus, it shows you’re serious about joining our team!

How to prepare for a job interview at Eisai

Know Your Quality Standards

Familiarise yourself with GMP, GDP, and Annex 15 guidelines. Be ready to discuss how these standards apply to the role of a Quality Validation Specialist and share examples of how you've ensured compliance in past projects.

Showcase Your Technical Knowledge

Brush up on your understanding of electronic systems, CSV, and GAMP requirements. Prepare to explain complex technical concepts in simple terms, as this will demonstrate your ability to communicate effectively with both technical and non-technical stakeholders.

Prepare for Scenario-Based Questions

Expect questions that assess your problem-solving skills and judgement in quality oversight. Think of specific situations where you had to analyse user requirements or implement system improvements, and be ready to walk through your thought process.

Highlight Your Collaborative Skills

Eisai values effective communication and teamwork. Prepare examples of how you've built relationships within teams or with external partners, and be ready to discuss how you can contribute to a collaborative working environment.