ROLE OVERVIEW
An exciting opportunity for a Director of GMP Operations to join a leading BioPharma Contract Development and Manufacturing Organisation (CDMO) based in Kent. Our client is seeking a dynamic leader to oversee and direct manufacturing processes, ensure compliance with strict industry standards, and drive operational excellence within their state-of-the-art facility.
This senior role offers a chance to influence strategic growth, optimise manufacturing efficiency, and lead multidisciplinary teams in a regulated environment. If you are a proven leader with extensive experience in biologics, pharmaceuticals, or biotech manufacturing, this could be the perfect fit for your career advancement.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the Director of GMP Operations will be varied however the key duties and responsibilities are as follows:
* Establish and manage a strategic direction for all manufacturing areas, aligning plans with broader business objectives and future growth initiatives.
* Oversee all aspects of production, ensuring products are manufactured and stored in compliance with documentation standards, quality protocols, and regulatory guidelines.
* Collaborate with Engineering, Maintenance, and Validation teams to maintain facilities and equipment, ensuring validations are completed and standards are met.
* Provide leadership and technical expertise across departments such as Process Development, Tech Ops, and Analytical Services to build capabilities for BioPharma CDMO services.
* As the Manufacturing Director, you will act as a key member of the senior management team, driving continuous improvement programs, managing budgets, and ensuring maximum asset utilization while maintaining cGMP standards.
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the Director of GMP Operations we are looking to identify the following on your profile and past history:
* A Degree or higher level in Business Management, Industrial Engineering, Life Sciences, or a related field.
* Proven leadership experience of at least 10 years in a high-volume manufacturing facility within the biotech, pharmaceutical, or medical device sectors.
* Extensive knowledge of cGMP standards, EU GMP/MHRA guidelines, and Quality Management Systems, including CAPA management, deviations, and audits.
1. WHAT’S IN IT FOR YOU?
This role offers a unique chance to lead within a cutting-edge, regulated environment, with the opportunity to shape strategic growth initiatives and influence industry standards. You will join a company committed to operational excellence and continuous development, in a facility that values innovation, safety, and quality.
Key Words: Leadership / Manufacturing / BioPharma / CDMO / GMP / Regulatory Compliance / Operational Excellence / Team Management / Strategic Planning / Continuous Improvement
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.