Jobs at Mopson Pharmaceutical Limited

Key Responsibilities

• Production Oversight: Manage the production line from raw materials to finished products, ensuring adherence to GMP guidelines and other regulatory standards.
• Quality Control: Conduct regular inspections, testing, and validation of equipment, processes, and products to maintain established quality standards.
• Process Optimization: Collaborate with the production team to develop and optimize manufacturing processes, identify areas for improvement, and implement innovative solutions.
• Documentation and Record Keeping: Maintain accurate documentation of production activities, including batch records and inventory management.
• Compliance: Ensure compliance with regulatory requirements, including those related to safety, security, and environmental regulations.
• Staff Training and Supervision: Provide training and support to production staff on pharmaceutical processes, safety protocols, and best practices.
• Problem-Solving: Address any production-related issues promptly and implement corrective actions as necessary.
• Inventory Management: Monitor inventory levels, assist in managing raw materials, and ensure the availability of necessary supplies.
• Collaboration: Work collaboratively with the quality assurance team to investigate and resolve product quality issues.

Requirements

• The candidates should possess a Bachelor's Degree in relevant fields with 0 - 2 years work experience.

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Job Summary

• Quality Assurance (QA) Manager will beresponsible for ensuring that products and processes meet quality standards and regulatory requirements.
• They oversee the development and implementation of quality management systems, monitor testing, and lead the QA team.Key responsibilities include reviewing documentation, handling deviations, managing audits, and providing training.

Key Responsibilities

• Quality Management System (QMS) Development and Implementation: Establishing and maintaining the company's QMS to ensure compliance with regulatory standards (e.g., GMP, GDP).
• Compliance: Staying up-to-date on regulatory changes and ensuring that all processes and products meet current regulations.
• Team Leadership: Managing the QA team, providing guidance and support, and ensuring that team members are competent and motivated.
• Documentation Review and Approval: Reviewing and approving documentation related to manufacturing, testing, and release of products.
• Deviation Management: Investigating and managing deviations from standard operating procedures (SOPs).
• Audit Management: Preparing for and leading regulatory inspections and customer audits.
• Quality Metrics and Reporting:Implementing and monitoring quality metrics, and reporting findings to management.
• Continuous Improvement: Identifying areas for improvement in quality systems and processes.
• Training and Development:Providing training to staff on quality procedures and regulations.
• Supplier Quality: Working with suppliers to ensure the quality of raw materials and components.
• Product Release: Approving the release of products for distribution.
• Collaborative Work: Working with cross-functional teams to address quality issues and ensure timely resolution.
• Risk Management: Identifying and mitigating potential risks to product quality.

Qualifications and Skills

• Candidate should possess a Bachelor's Degree with 5 - 6 years work experience.
• Knowledge: In-depth knowledge of GMP, GDP, GLP, and other relevant regulations.
• Skills: Strong leadership, communication, and interpersonal skills;excellent analytical and problem-solving skills.