Back to Job SearchROLE OVERVIEW
An exciting opportunity for a Validation & Qualification Specialist to join a leading pharmaceutical organization focusing on biological drug substance validation. This role offers the chance to be part of a dynamic team, supporting routine validation activities while contributing to crucial quality assurance processes within a renowned biotech environment. You will play an integral role in ensuring compliance with GMP standards and facilitating the qualification of key equipment and processes.
Our client is seeking a proactive and dependable professional to support site validation efforts, with flexibility around the role’s transitional nature and upcoming project pipeline. This position provides an excellent platform for those looking to deepen their expertise in biological pharmaceutical validation within an innovative company.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the Validation & Qualification Specialist will be varied however the key duties and responsibilities are as follows:
• Perform routine qualification and validation activities related to small-scale equipment, process parameters, and building validation to ensure compliance with GMP standards.
• Validate drug substance production equipment, including vessels, bioreactors, and transfer lines, supporting manufacturing consistency and quality.
• Conduct periodic review activities and support project-related activities depending on integration and skills development.
• Support qualification efforts during site validation projects and collaborate with internal stakeholders to meet project requirements.
• As the Validation & Qualification Specialist, you will work independently, managing multiple tasks simultaneously while maintaining high standards of quality and compliance.
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the Validation & Qualification Specialist we are looking to identify the following on your profile and past history:
• A Degree or higher level in Engineering or a relevant field.
• Proven experience in pharmaceutical Qualification & Validation, with a solid understanding of GMP requirements and validation strategies.
• Ability to work with multiple internal stakeholders across departments and fluently communicate in French; basic to intermediate English skills are acceptable.
Key Words: Validation / Qualification / GMP / Pharmaceutical / Biotech / Bioreactors / Equipment Validation / Remote Work / Stakeholder Collaboration / Biological Drug Substance
"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.
