Join Our Team
- Production Manager
Job Responsibilities:
1.Coordinate all production activities comprehensively to ensure the execution of the production plan.
2.Organize and optimize production processes to continuously improve product quality.
3.Organize and optimize the production system and quality management system to ensure compliance and legality.
4.Organize and optimize the calculation of production efficiency, and establish a production staff evaluation system.Qualifications:
1.Master’s degree in Pharmaceutical Engineering, Pharmacy, Chemical Engineering, or related fields.
2.Familiar with chemical raw material synthesis processes, GMP management procedures, and national pharmaceutical regulations.
3.At least 4 years of experience in production management; candidates who have participated in on-site drug review are preferred.
4.Strong communication, coordination, and professional guidance skills.
- Production Technician
Job Responsibilities:
1.Work under the leadership and direction of senior management.
2.Strictly follow the operational procedures of the department, adhere to the company's safety, quality, and hygiene regulations, and willingly comply with work arrangements.
3.Strictly carry out operations according to the process requirements of the position.
4.Enhance efficiency awareness, strengthen coordination and cooperation, and ensure the timely completion of production tasks.
5.Constantly check the operational status of equipment, perform daily maintenance, report any issues promptly, and ensure safe production operations.
6.If any quality issues with the products are detected during the production process, stop production and deal with or report the issue promptly.
7.At the end of each day's process, ensure the work area and machinery are cleaned and cleared.Qualifications:
1.Bachelor’s degree in Pharmaceutical Engineering, Pharmacy, Chemical Engineering, or a related field, with over 2 years of work experience.
2.Candidates with experience in the synthesis of active pharmaceutical ingredients are preferred.
3.Experience participating in the construction of GMP production lines is preferred.
- Quality Management Specialist
Job Responsibilities:
1.Responsible for organizing the assessment of deviations in the company's production quality management process, conducting investigations into deviations, and tracking the implementation of measures.
2.Complete other daily tasks and various assignments delegated by leadership.Qualifications:
1.Bachelor’s degree in Pharmaceutical Engineering, Pharmacy, or a related field.
2.More than 2 years of experience in production quality management, including at least 1 year in QC management.
3.Familiar with national GMP regulatory requirements and experienced in GMP quality system audits.
4.Possess strong written communication skills to draft investigation and assessment reports.
