Join a highly respected pharmaceutical organization renowned for its commitment to quality, safety, and innovation. With an emphasis on compliance and excellence, this company offers an inclusive and supportive environment where your expertise will directly contribute to patient safety and product quality. You’ll have the chance to work alongside dedicated professionals and develop your career in a business that values integrity and growth.
Onsite full-time - 10am - 7pm working hours
Responsibilities / Role
In this role, you will:
Ensure compliance with statutory regulations and GMP/GDP requirements. Implement and maintain the company’s Quality Management System.
Investigate non-compliance issues and manage corrective actions.
Approve raw materials, intermediates, and finished products.
Organize and audit manufacturing documentation and records.
Perform internal audits and manage change control procedures.
Oversee validations for equipment, facilities, and processes.
Qualifications & Experience
Degree in Pharmaceutical Sciences (minimum BSc) or related discipline.
At least 6 months’ experience within a GMP-regulated pharmaceutical environment.
Solid understanding of Quality Management Systems, SOPs, validation protocols, and regulatory guidelines.
Additional Skills
Strong knowledge of QMS and validation protocols.
Ability to review and approve technical documentation.
Experience with internal audits, supplier assessments, and CAPA systems.
Familiarity with raw material testing and compliance standards.
Experience with HVAC systems operation.
Knowledge of MHRA requirements and product recalls.
Proficiency in environmental monitoring techniques.
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