Validation Specialist

Hyper Recruitment Solutions Ltd; England; On-site; GBP 35,000 - 55,000; Full time

Job summary

An established industry player in the pharmaceutical sector is seeking a Validation Specialist to enhance their quality assurance team. In this pivotal role, you will utilize your technical and regulatory expertise to ensure compliance with stringent manufacturing processes. This position involves conducting validation for equipment and systems, managing validation projects, and developing comprehensive Site Validation Master Plans. Join a dynamic team dedicated to excellence in pharmaceutical manufacturing, where your contributions will have a significant impact on product quality and regulatory compliance. If you are passionate about ensuring the highest standards in the life sciences, this opportunity is perfect for you.

Qualifications

• Relevant degree in Chemical Engineering or related field.
• Proven experience in pharmaceutical validation processes.

Responsibilities

• Conduct validation processes for equipment and systems.
• Manage validation projects ensuring compliance with standards.

Skills

Pharmaceutical Validation

GMP

Regulatory Compliance

Data Analysis

Education

Degree in Chemical Engineering

Degree in Pharmaceutical Sciences

Degree in Mechanical Engineering

Tools

Validation Protocols

Computer System Validation

Job description

14325Permanent Competitive Site Based Herefordshire, United Kingdom Updated on: 06-03-2025

ROLE OVERVIEW

A leading pharmaceutical company based in the Hertfordshire area is seeking a Validation Specialist to join their dynamic team. This role offers the chance to leverage your technical and regulatory expertise in a rewarding environment. As the Validation Specialist, you will play a crucial role in ensuring the quality and compliance of pharmaceutical manufacturing processes.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Validation Specialist will be varied; however, the key duties and responsibilities are as follows:

1. Conducting validation processes for equipment, systems, and cleaning procedures to ensure compliance with regulatory standards.
2. Managing validation projects from planning through execution and reporting, ensuring timely and budget-compliant completion.
3. Developing and managing Site Validation Master Plans and performing quality and compliance gap assessments.
4. Writing, reviewing, and approving validation protocols (IQ/OQ/PQ) and reports.

ROLE REQUIREMENTS:

To be successful in your application to this exciting role as the Validation Specialist, we are looking to identify the following on your profile and past history:

1. Relevant degree in Chemical Engineering, Pharmaceutical Sciences, Mechanical Engineering, or a related field.
2. Proven industry experience in pharmaceutical validation processes, including GMP.
3. A working knowledge and practical experience with regulatory guidelines such as MHRA, FDA, and EMA standards.

Key Words:
Validation Specialist / Pharmaceutical Validation / GMP / Equipment Validation / Process Validation / Cleaning Validation / Computer System Validation / Regulatory Compliance / Validation Protocols / Data Analysis

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.