Validation Specialist – Pharma
Validation Specialist – Pharma

Validation Specialist – Pharma

Full-Time 32000 - 54000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Join our team as a Validation Specialist, focusing on production and process validation.
  • Company: Be part of a leading Pharmaceutical Manufacturer known for specialist pharmaceuticals.
  • Benefits: Enjoy a competitive salary of £37K - £45K with standard day shifts and occasional flexibility.
  • Why this job: This role offers a chance to make a real impact in a dynamic environment.
  • Qualifications: Degree level education or equivalent experience in Pharmaceutical Production is required.
  • Other info: Experience in Lean Six Sigma methodologies is a plus!

The predicted salary is between 32000 - 54000 £ per year.

Do you have experience of production and process validation? Are you looking for a new challenge with a leading Pharmaceutical Manufacturer?A manufacturer of specialist pharmaceuticals is currently seeking a Validation Specialist to join the production team at their site in Guildford. The role will involve taking on production and process validation responsibility for the production team. This is a permanent, full-time role. Predominantly standard day shifts Monday to Friday, with a requirement for occasional weekend or night shifts. £37K – £45KRole OverviewResponsible for validation activities to support new products/processes in compliance with cGMP and all relevant guidelines.Supporting the QA team to generate documentation (IQ, OQ, PQ, RQ etc.)Provide technical expertise and troubleshooting issues related to production and processes and identify areas for improvement.RequirementsEducated to Degree level or equivalent in relevant discipline or equivalent relevant experience in Pharmaceutical Production.Strong experience in troubleshooting and continuous improvement with respect to processes used in cGMP Production.Previous experience in production and process validation specifically is essential (as opposed to QC/Method Validation).Knowledge of and experience with Lean Six Sigma and similar methodologies is highly beneficial.For more information, please contact Louis Williams. #J-18808-Ljbffr

Validation Specialist – Pharma employer: JobLeads GmbH

Join a leading Pharmaceutical Manufacturer in Guildford, where we prioritise employee growth and development within a collaborative work culture. As a Validation Specialist, you will benefit from competitive salaries, standard day shifts, and opportunities to engage in continuous improvement initiatives, all while contributing to the production of specialist pharmaceuticals that make a difference in people's lives.
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Contact Detail:

JobLeads GmbH Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Validation Specialist – Pharma

Tip Number 1

Make sure to highlight your specific experience in production and process validation during any conversations you have. This role requires a strong background in these areas, so be ready to discuss your previous projects and how they relate to the responsibilities of the Validation Specialist position.

Tip Number 2

Familiarise yourself with cGMP guidelines and Lean Six Sigma methodologies. Being able to demonstrate your knowledge and application of these standards can set you apart from other candidates and show that you're well-prepared for the challenges of the role.

Tip Number 3

Network with professionals in the pharmaceutical industry, especially those who work in validation roles. Engaging with others in the field can provide valuable insights and may even lead to referrals or recommendations for the position at StudySmarter.

Tip Number 4

Prepare to discuss your troubleshooting skills and examples of continuous improvement initiatives you've led. The hiring team will be looking for candidates who can not only validate processes but also enhance them, so come equipped with relevant examples.

We think you need these skills to ace Validation Specialist – Pharma

Production and Process Validation
cGMP Compliance
Documentation Generation (IQ, OQ, PQ, RQ)
Technical Expertise in Pharmaceutical Production
Troubleshooting Skills
Continuous Improvement Methodologies
Lean Six Sigma
Attention to Detail
Analytical Skills
Problem-Solving Skills
Communication Skills
Team Collaboration
Adaptability to Shift Patterns

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in production and process validation. Use specific examples that demonstrate your expertise in cGMP compliance and any relevant methodologies like Lean Six Sigma.

Craft a Strong Cover Letter: Write a cover letter that clearly outlines your motivation for applying to the Validation Specialist role. Mention how your background aligns with the job requirements and express your enthusiasm for working with a leading Pharmaceutical Manufacturer.

Highlight Relevant Experience: In your application, emphasise your previous roles related to validation activities. Detail your experience with documentation such as IQ, OQ, PQ, and RQ, and provide examples of how you've contributed to continuous improvement in production processes.

Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in the pharmaceutical industry.

How to prepare for a job interview at JobLeads GmbH

Showcase Your Validation Experience

Make sure to highlight your specific experience in production and process validation during the interview. Be prepared to discuss past projects where you successfully implemented validation protocols and how they contributed to compliance with cGMP standards.

Demonstrate Problem-Solving Skills

Since troubleshooting is a key part of the role, come equipped with examples of challenges you've faced in previous positions. Explain how you identified issues and the steps you took to resolve them, showcasing your analytical thinking and technical expertise.

Familiarise Yourself with Lean Six Sigma

If you have experience with Lean Six Sigma methodologies, be ready to discuss how you've applied these principles in your work. If not, do some research on the basics so you can speak knowledgeably about continuous improvement processes.

Prepare for Technical Questions

Expect to answer technical questions related to validation documentation such as IQ, OQ, PQ, and RQ. Brush up on these concepts and be ready to explain their importance in the validation process, as well as any relevant experiences you have had with them.

Validation Specialist – Pharma
JobLeads GmbH
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  • Validation Specialist – Pharma

    Full-Time
    32000 - 54000 £ / year (est.)

    Application deadline: 2027-07-31

  • J

    JobLeads GmbH

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