We are seeking a motivated and enthusiastic Validation Engineer/Specialist to join our on-site team. This is a fantastic opportunity for an individual looking to develop their validation expertise and contribute provide crucial business support.
As part of a small and collaborative engineering team, you will work closely with our existing Manufacturing and Process Engineers to complete the necessary validation documentation and support ongoing projects. This role offers a unique chance to gain hands-on experience across the validation lifecycle in a dynamic environment.
Key Responsibilities:
- Support the validation activities for our new and existing equipment.
- Take ownership of and progress validation projects.
- Create and execute validation documentation including IQ, OQ, PQ, and URS.
- Manage the approval process for validation documents through collaboration with QA, QC, and Manufacturing departments.
- Provide support to the existing engineering team to progress validation tasks for NPI.
- Contribute to the overall validation workload, helping to address projects that have been put on hold.
- Ensure all validation activities are conducted in compliance with relevant regulations and internal procedures.
Qualifications and Experience:
- A degree in a Science, Engineering, or a related technical discipline.
- Initial exposure to /experience of validation principles within a regulated environment (e.g., pharmaceutical, medical device, food).
- Strong attention to detail and a commitment to producing high-quality documentation.
- Excellent organizational and time management skills.
- Good communication and interpersonal skills, with the ability to work effectively within a team.
- A proactive approach to learning and problem-solving.
- Ability to follow procedures and work within a structured framework.
- Must be able to work full-time on-site.
