Validation Engineer

Hydrokem Aerosols Ltd; Birkenhead; On-site; GBP 30,000 - 45,000; Full time

Job summary

A manufacturing company in Wirral is seeking a Validation Officer to oversee equipment qualification and process validation, and ensure compliance with Quality Management System standards. The ideal candidate should have at least 3 years' experience in validation, strong knowledge of quality control processes, and excellent communication skills. This is a full-time position with responsibilities that include training staff and conducting audits.

Qualifications

• Minimum of 3 years of experience in a validation role, preferably in a manufacturing environment.
• Strong knowledge of Quality Control processes and procedures.
• Excellent written and verbal communication skills.

Responsibilities

• Compile validation protocols and ensure proper documentation.
• Conduct equipment qualification and process validation activities.
• Collaborate with various departments to ensure timely completion of validation tasks.
• Train production staff on in-process control and guidance on Batch Manufacturing Records (BMRs).
• Promote the Quality Management System (QMS) and coach staff on procedures.

Skills

Quality Control processes

Excellent communication skills

Team player

Problem-solving techniques

Job description

Hydrokem Aerosols Ltd, located on the Wirral, specialises in the manufacture of aerosol and bag on valve products. We supply to a wide range of market sectors including personal care, healthcare/medical devices, veterinary, household, automotive and technical. Hydrokem Aerosols is part of Clinimed Holding Limited, a group of companies founded in 1982.

If you have passion for learning and want to build a career with a company that values its employees and is dedicated to making a positive impact in the world, we encourage you to apply.

Job Summary

We are seeking a Validation Officer to oversee equipment qualification, process validation, and compliance with Quality Management System (QMS) standards. The role involves compiling validation protocols, conducting audits, training staff, and supporting regulatory and customer audits. The ideal candidate will have experience in a validation role within a manufacturing environment, strong knowledge of quality control processes, and excellent communication skills.

Main Duties & Responsibilities

• Compile validation protocols and ensure proper documentation.
• Conduct equipment qualification and process validation activities.
• Collaborate with various departments to ensure timely completion of validation tasks.
• Provide support to the Quality Manager as needed.
• Train production staff on in-process control and guide them in completing Batch Manufacturing Records (BMRs).
• Promote the Quality Management System (QMS) by coaching staff on Standard Operating Procedures (SOPs), documentation, and best working practices.
• Assist staff during investigations by applying problem-solving techniques.
• Support the deployment and implementation of new documentation.
• Assist with on-site customer and external regulatory audits.
• Conduct internal and supplier audits as per the audit plan.
• Collect and analyze data to prepare quality metrics.
• Provide Quality Assurance (QA) support across departments to ensure compliance with QMS, customer standards, and regulatory requirements.
• Manage change processes effectively through proper change controls, information dissemination, and staff training.

Personal Specifications

• Minimum of 3 years of experience in a validation role, preferably in a manufacturing environment.
• Strong knowledge of Quality Control processes and procedures.
• Excellent written and verbal communication skills.
• A strong team player with the ability to work independently when needed.

Additional Details

• Seniority level: Associate
• Employment type: Full-time
• Job function: Quality Assurance and Manufacturing
• Industries: Manufacturing, Pharmaceutical Manufacturing, and Chemical Manufacturing
• Location: Wirral, England, United Kingdom