Job Description
Our company are a leading manufacturing pharmaceutical firm dedicated to delivering high-quality products while adhering to the highest safety and regulatory standards. We are currently seeking an experienced and dynamic Quality Control Area Manager to join our team. This role is critical in maintaining our operations’ efficiency and ensuring compliance with Good Manufacturing Practices (GMP) standards.
Key Responsibilities:
Area Management:
Oversee operations to ensure efficiency and minimize downtime Team Development:
Align team objectives with site goals and provide performance feedback Training:
Train new staff and maintain up-to-date training documentation Performance Management:
Implement the performance management process and handle employee relations issues Quality Assurance:
Ensure GMP compliance in testing of water samples, intermediates, and finished products Environmental Monitoring:
Lead departmental meetings and address adverse trends through CAPA's QMS Compliance:
Ensure adherence to CAPA's, change controls, and deviations Technical Support:
Enhance test methods and ensure robustness in procedures Documentation:
Develop and maintain specifications and SOP's per GMP guidelines Batch Release:
Manage timely release of batches in line with commitments Safety Leadership:
Promote safety and maintain proper documentation in the lab Audit Support:
Assist in inspections and implement corrective actions for any findings Continuous Improvement:
Identify opportunities for productivity enhancement and cost savings Qualifications: Bachelor’s degree in a relevant field (e.g., Life Sciences, Quality Control, or related discipline) Significant experience in a quality control or quality assurance role within a regulated environment Strong understanding of GMP, pharmacopoeial standards, and quality management systems Excellent leadership, communication, and interpersonal skills Proven ability to manage teams, drive performance and facilitate training Proficiency in SAP or similar laboratory information management systems
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Oversee operations to ensure efficiency and minimize downtime Team Development:
Align team objectives with site goals and provide performance feedback Training:
Train new staff and maintain up-to-date training documentation Performance Management:
Implement the performance management process and handle employee relations issues Quality Assurance:
Ensure GMP compliance in testing of water samples, intermediates, and finished products Environmental Monitoring:
Lead departmental meetings and address adverse trends through CAPA's QMS Compliance:
Ensure adherence to CAPA's, change controls, and deviations Technical Support:
Enhance test methods and ensure robustness in procedures Documentation:
Develop and maintain specifications and SOP's per GMP guidelines Batch Release:
Manage timely release of batches in line with commitments Safety Leadership:
Promote safety and maintain proper documentation in the lab Audit Support:
Assist in inspections and implement corrective actions for any findings Continuous Improvement:
Identify opportunities for productivity enhancement and cost savings Qualifications: Bachelor’s degree in a relevant field (e.g., Life Sciences, Quality Control, or related discipline) Significant experience in a quality control or quality assurance role within a regulated environment Strong understanding of GMP, pharmacopoeial standards, and quality management systems Excellent leadership, communication, and interpersonal skills Proven ability to manage teams, drive performance and facilitate training Proficiency in SAP or similar laboratory information management systems
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