Purification Production Supervisor

Description

Position Summary: Supervises and executes weekly and monthly manufacturing programs, ensuring regulatory compliance and staff training in a pharmaceutical company. Key Highlights: 1. Leadership and supervision of sterile drug manufacturing processes. 2. Compliance with and execution of manufacturing programs and regulatory requirements. 3. Development and updating of SOPs and staff training. Pharmaceutical Company Seeks Purification Production Supervisor ***Requirements:*** · Bachelor's degree in Chemical Sciences, Biological Sciences, or Biotechnology (degree certificate required) · 2 years of experience in sterile drug and/or biological product manufacturing · Experience in injectable product manufacturing · English level A2 (preferred) · Training in Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) · Knowledge of Quality Management Systems (QMS) · Basic microbiology concepts ***Main Responsibilities:*** · Implement and execute weekly and monthly manufacturing programs · Ensure all activities comply with GMP, GDP, and internal and regulatory guidelines throughout the production process · Verify that manufacturing and packaging processes meet specified parameters, process controls, and current qualification status of areas and equipment · Report activity progress to immediate supervisor timely and accurately · Develop, update, and maintain departmental SOPs, and track training and competency development for assigned personnel ***Activities:*** · Request weekly production schedule from management and assign daily tasks to staff · Request consumables required for production areas · Supervise and ensure accurate recording of activities in master documentation (Manufacturing Instructions, batch records, and GDP forms) · Support operators in operating process equipment · Verify equipment settings and product specifications for in-process and finished products · Report equipment damage or potential operational risks · Ensure timely closure and submission of manufacturing files to Quality Assurance · Daily reporting of activities, process times, absences, and disabilities · Report critical or major deviations related to production documents, manufacturing, or QMS · Draft, verify validity of, and update departmental SOPs · Train and coach technical and operational staff per the procedures matrix ***Key Competencies:*** · Process Control and Execution · Results Orientation / Goal Achievement · Leadership and Process Supervision · Conflict Management · Tactical or Operational Decision-Making · Working Under Pressure · Accountability · Regulatory Compliance Service-Oriented Attitude Salary: $21,000\.00 per month Benefits: * Major medical expense insurance Work Location: On-site employment