The document outlines the responsibilities of a Quality Control Supervisor position at PT. Biotis Pharmaceuticals Indonesia. The supervisor will oversee quality control activities to ensure compliance with Good Manufacturing Practice and Good Laboratory Practice. Key responsibilities include supervising laboratory testing, approving quality control procedures, collecting and analyzing data, and ensuring quality control supports production. The position requires a pharmacy or apothecary degree and 2 years laboratory experience. Duties are focused on maintaining and improving quality systems.
The document outlines the responsibilities of a Quality Control Supervisor position at PT. Biotis Pharmaceuticals Indonesia. The supervisor will oversee quality control activities to ensure compliance with Good Manufacturing Practice and Good Laboratory Practice. Key responsibilities include supervising laboratory testing, approving quality control procedures, collecting and analyzing data, and ensuring quality control supports production. The position requires a pharmacy or apothecary degree and 2 years laboratory experience. Duties are focused on maintaining and improving quality systems.
The document outlines the responsibilities of a Quality Control Supervisor position at PT. Biotis Pharmaceuticals Indonesia. The supervisor will oversee quality control activities to ensure compliance with Good Manufacturing Practice and Good Laboratory Practice. Key responsibilities include supervising laboratory testing, approving quality control procedures, collecting and analyzing data, and ensuring quality control supports production. The position requires a pharmacy or apothecary degree and 2 years laboratory experience. Duties are focused on maintaining and improving quality systems.
The document outlines the responsibilities of a Quality Control Supervisor position at PT. Biotis Pharmaceuticals Indonesia. The supervisor will oversee quality control activities to ensure compliance with Good Manufacturing Practice and Good Laboratory Practice. Key responsibilities include supervising laboratory testing, approving quality control procedures, collecting and analyzing data, and ensuring quality control supports production. The position requires a pharmacy or apothecary degree and 2 years laboratory experience. Duties are focused on maintaining and improving quality systems.
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JOB DESK
PAGE 1 FROM 5
Job Desk No. :
QC SUPERVISOR Effective Date :
PT. BIOTIS PHARMACEUTICALS INDONESIA Review Date :
DEPARTMENT: SECTION: Supersedes : New
QUALITY CONTROL Date :
DISUSUN OLEH (Written By) : DIPERIKSA OLEH (Checked By) : DISETUJUI OLEH (Approved By) :
Sussi W. K Ita R Ita R
Quality Manager HRD Staff HRD Staff
IDENTIFICATION OF POSITION Position Name: Supervisor Report to : Quality Manager Supervise : Microbiology and Chemical Lab Analyst
JOB SUMMARY Ensuring that all of the functions of quality control system is implemented at PT. Biotis Pharmaceuticals Indonesia (BPI). Responsible for the laboratory testings and the quality of output with goal to support the quality management system. Organize all of the work plans in quality control department. Support all the departments in line with production and quality system. Conducts the jobs based on Good Manufacturing Practice and Good Laboratory Practice requirements.
DESCRIPTION OF DUTIES AND RESPONSIBILITIES
Prepare documents regarding quality control methods and standards. Supervise and monitoring all of quality control activities regarding media and equipments preparation, laboratory testings, cleaning, and maintenance. Ensure all testing and observation process appropriate with the established procedures. Ensure all quality control activities appropriate with the quality management system. Ensure all quality control activities support the production lines. Responsible to establish inspection protocols, define sampling procedures, and determine equipments and mechanism to be used in testing process. Responsible to approve specification, sampling methods, testing methods, and other quality control procedures. Responsible the work, such as the implementation of calibration, qualification, and validation as well as the implementation of employee training both job skills and general
Job Desk Code xxxx Dated xx/yy/zzzz Confidential
JOB DESK PAGE 2 FROM 4
Job Desk No. :
QC SUPERVISOR Effective Date :
PT. BIOTIS PHARMACEUTICALS INDONESIA Review Date :
DEPARTMENT: SECTION: Supersedes : New
QUALITY MANAGEMENT QUALITY CONTROL Date :
WRITTEN BY : CHECKED BY : APPROVED BY :
Sussi W. K …………Name………….. …………Name…………..
Quality Manager Position Position
(CPOB) and then documenting it.
Responsible for collecting and saving data and analysis regarding all results in quality control laboratory. Suggest improvements for better and effective laboratory work mechanism. Suggest training requirement and planning for the improvement of personnel’s capabilities. Overseeing the administrative implementation of the QC Department's activities, all records ranging from tool usage notes, room records, reagent usage records, and media for product testing or retesting activities, as well as drug raw materials. Communicate and work together with all departments with the goal of optimum product quality. Develop and document various processes and prepare final reports.
JOB REQUIREMENTS TERMS
CRITERIA Sex Male or Female Age 25 – 30 years Formal Education Min. Graduated from Pharmacy/Apothecary Work Experience At least 2 years in laboratory working experience. Other Requirements Having knowledges in Good Laboratory Practice and Good Manufacturing Practice.
Job Desk Code xxxx Dated xx/yy/zzzz Confidential
JOB DESK PAGE 3 FROM 4
Job Desk No. :
QC SUPERVISOR Effective Date :
PT. BIOTIS PHARMACEUTICALS INDONESIA Review Date :
DEPARTMENT: SECTION: Supersedes : New
QUALITY MANAGEMENT QUALITY CONTROL Date :
WRITTEN BY : CHECKED BY : APPROVED BY :
Sussi W. K …………Name………….. …………Name…………..
Quality Manager Position Position
Having capability to prepare and conduct analysis methods.
Having good leadership and communication manner. Team work oriented. Good analyzing and interpretation skill.
AUTHORITIES To conduct all the work plans in quality control department. To establish inspection protocols, define sampling procedures, and determine equipments and mechanism to be used in testing process To supervise all of the laboratory quality testing process. To analyze and interpretate all of laboratory testing results. To have suggestions regarding improvement of quality control department.
DELEGATION Analyst
HISTORY Revision Effective date Reason of Change New
DISTRIBUTION QMD Manager HRD Manager
Job Desk Code xxxx Dated xx/yy/zzzz Confidential
JOB DESK PAGE 4 FROM 4
Job Desk No. :
QC SUPERVISOR Effective Date :
PT. BIOTIS PHARMACEUTICALS INDONESIA Review Date :
DEPARTMENT: SECTION: Supersedes : New
QUALITY MANAGEMENT QUALITY CONTROL Date :
WRITTEN BY : CHECKED BY : APPROVED BY :
Sussi W. K …………Name………….. …………Name…………..
Quality Manager Position Position
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