Total 5 help desk specialist job vacancies in Singapore

Mission Description:

• Review and authorize the release of products and raw materials to ensure compliance with Quality standards.
• Provide Quality oversight during the manufacturing process to ensure adherence to established protocols.
• Conduct GEMBA walks and GMP inspections to assess compliance and identify areas for improvement.
• Revise, review, and approve various procedures, including SOPs, forms, and Manufacturing Batch Records to ensure accuracy and regulatory compliance.

Profile Requirement:

• Experience in Quality Assurance or Quality Control within a regulated industry.
• Strong understanding of product and raw material release processes.
• Familiarity with Good Manufacturing Practices (GMP) and continuous improvement methodologies.
• Excellent attention to detail and communication skills.

Mission Description:

• Develop and maintain the Master Production Schedule (MPS) to ensure efficient production flow and meet customer demand.
• Utilize JDE for managing Bill of Materials (BOM) and Material Requirements Planning (MRP) to ensure accurate inventory levels and resource allocation.
• Collaborate with cross-functional teams, including production, procurement, and logistics, to align production plans with operational goals.
• Analyze production data and metrics to identify trends, optimize processes, and drive continuous improvement.
• Support inventory management efforts, including tracking materials and finished goods to minimize waste and improve efficiency.
• Communicate production schedules and updates to relevant stakeholders to ensure alignment and transparency.

Profile Requirement:

• Experience in manufacturing planning, with a strong understanding of MPS and JDE systems.
• Proficiency in Bill of Materials (BOM) management and Material Requirements Planning (MRP).
• Strong analytical skills and attention to detail.
• Excellent communication and teamwork abilities.
• Ability to thrive in a fast-paced manufacturing environment.
• Can Start by November

Mission Description:

• Oversee Quality compliance in validation processes, with an emphasis on Data Integrity.
• Collaborate with Subject Matter Experts to conduct gap analyses and risk evaluations prior to qualification efforts.
• Participate in investigations of validation discrepancies, aiding in the review and approval of discrepancy reports and ensuring CAPA closures.
• Review and authorize various validation documentation, such as protocols and reports.
• Provide assistance and solutions for validation-related inquiries and challenges.
• Evaluate and approve routine SOPs, forms, and other relevant documents, including Manufacturing Batch Records.

Profile Requirement:

• Background in Quality Assurance or Quality Control within a regulated setting.
• Familiarity with validation processes and principles of Data Integrity.
• Strong analytical and problem-solving capabilities.
• Excellent communication and collaborative skills.
• Can start by November.

Mission Description:

• Lead and execute preventive maintenance and calibration maintenance workflows to ensure equipment operates efficiently and meets compliance standards.
• Oversee SAP integration and migration efforts related to maintenance, acting as the primary expert and administrator for the system.
• Collaborate with various teams to optimize maintenance operations and enhance overall efficiency.
• Provide training and support to team members on maintenance procedures and SAP functionalities.
• Analyze maintenance data to identify trends, streamline processes, and ensure adherence to regulatory requirements.
• Develop and maintain documentation and reporting systems related to maintenance activities.

Profile Requirement

• Strong experience in maintenance management, particularly in preventive and calibration processes.
• Expert-level proficiency in SAP integration and administration.
• Excellent analytical and problem-solving capabilities.
• Strong communication and leadership skills.
• Ability to work effectively in a dynamic environment.
• Can start by November.

Job Description:

• Review and approve electronic batch records to ensure compliance with regulatory standards
• Identify and address discrepancies or errors in electronic batch records
• Collaborate with production and quality teams to resolve issues related to electronic batch records
• Conduct internal audits of electronic batch records and document findings
• Provide training on electronic recordkeeping practices to relevant personnel
• Contribute to continuous improvement initiatives related to electronic batch record processes
• Maintain electronic record management systems and ensure data integrity

Requirement:

• Bachelor's degree in a relevant field (e.g., pharmaceutical sciences, chemistry, biology)
• Knowledge of regulatory requirements related to electronic batch records in the pharmaceutical industry
• Strong attention to detail and analytical skills
• Excellent communication and collaboration abilities
• Ability to work effectively in a team environment
• Prior experience in a pharmaceutical or related industry is a plus