Back to Job SearchROLE OVERVIEW
We are currently looking for a Validation Engineer to join a leading pharmaceutical manufacturing environment to support key automation revamping projects. This is an exciting full-time opportunity for a proactive and experienced professional to collaborate with our client’s team and contribute to impactful projects that enhance process efficiency and compliance.
An ideal candidate will possess a strong background in Qualification & Validation activities, with the ability to operate autonomously and communicate effectively with stakeholders at all levels. The role requires a quick ramp-up and a flexible approach, including a mix of onsite and remote work, within a dynamic and fast-paced setting.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the Qualification & Validation SME will be varied however the key duties and responsibilities are as follows:
- Define and develop the Qualification & Validation (Q&V) strategy for assigned projects.
- Lead and execute qualification activities, including mechanical qualification and Computer System Validation (CSV).
- Write, review, and maintain all relevant documentation such as protocols, qualification reports, and validation reports.
- Manage Q&V projects from initiation through to closure, ensuring timelines and quality standards are met.
- Communicate and collaborate with project stakeholders to ensure alignment and project success.
- As the Qualification & Validation SME, you will take overall responsibility for validation deliverables and project execution.
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the Qualification & Validation SME we are looking to identify the following on your profile and past history:
- A Degree or higher level in a relevant field (e.g., Pharmaceutical Chemistry, Quality Assurance, Quality Management).
- Proven experience of 4–5 years in Qualification & Validation, with a strong emphasis on CSV; manufacturing experience is highly advantageous.
- Demonstrable ability to develop Q&V strategies, execute validation activities, and compile comprehensive documentation.
- Fluency in French (mandatory) and good written English skills.
- Ability to work independently with minimal onboarding, adapting quickly to project needs and environment.
Key Words: Qualification / Validation / CSV / Automation / Manufacturing / Validation Strategy / Stakeholder Communication / Pharmaceutical
"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career."
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
