Job description
What You Need to Know:
Here’s your chance to step into a dynamic Validation Engineer position within a cGMP regulatory environment. If you’re an energetic, experienced engineer ready for a new challenge, this role offers variety and the opportunity to make an impact across multiple specialised validation areas.
Your New Job:
You’ll be responsible for supporting various validation projects, particularly around sterilisation, cleaning processes, temperature mapping, and more. This position will see you collaborating closely with different departments and contributing to compliance and continuous improvement efforts. Strong teamwork and independent working skills are key for success.
Key Duties and Responsibilities:
What Are We Looking For?
Apply for This Job:
Apply for this job now or get in touch with Consultant Name on Consultant Phone Number for more information.
Compliance Statement:
By applying, you are giving consent for Matrix Recruitment to contact you about this job. We collect your data for recruitment purposes only and will retain it for the duration required as outlined in our privacy policy. All CVs are treated in strict confidence and will not be submitted to any client without your prior knowledge and permission. Please note that due to the high volume of applications, we can only respond to candidates who meet the criteria for the role.
We Value Your Trust.
Here’s your chance to step into a dynamic Validation Engineer position within a cGMP regulatory environment. If you’re an energetic, experienced engineer ready for a new challenge, this role offers variety and the opportunity to make an impact across multiple specialised validation areas.
Your New Job:
You’ll be responsible for supporting various validation projects, particularly around sterilisation, cleaning processes, temperature mapping, and more. This position will see you collaborating closely with different departments and contributing to compliance and continuous improvement efforts. Strong teamwork and independent working skills are key for success.
Key Duties and Responsibilities:
- Prepare, review, and execute validation documentation and cycle development studies.
- Support and manage change controls and technical issue resolution.
- Engage with cross-functional teams during qualification activities.
- Lead or participate in investigations, root cause analysis, and technical reviews.
- Serve as validation representative on wider projects and forums.
- Uphold cGMP standards and manage documentation, risk assessments, and compliance actions.
- Participate in regulatory audits and submissions as required.
- Foster a safe and compliant work culture.
What Are We Looking For?
- Relevant qualification in Applied Pharmaceutical/Biological/Chemical sciences or Engineering.
- Significant experience in a comparable validation or engineering role within a GMP environment.
- Knowledge of CTU equipment qualification, thermal mapping, process/equipment validation, and deviation/change control management.
- Experience with technical/project leadership.
- Proficiency in data analysis, report writing, and Microsoft Office applications.
- Excellent communication and interpersonal skills.
- Evidence of ongoing professional development desirable.
Apply for This Job:
Apply for this job now or get in touch with Consultant Name on Consultant Phone Number for more information.
Compliance Statement:
By applying, you are giving consent for Matrix Recruitment to contact you about this job. We collect your data for recruitment purposes only and will retain it for the duration required as outlined in our privacy policy. All CVs are treated in strict confidence and will not be submitted to any client without your prior knowledge and permission. Please note that due to the high volume of applications, we can only respond to candidates who meet the criteria for the role.
We Value Your Trust.
