Kerja Sepenuh Masa Supervisor - Leader, Production, Gaji tinggi MYR 3,075 di Pharmaniaga LifeScience Selangor - Maukerja

Leader:

1) To assist the team leader, monitor and operate the activities in SVI to ensure products are manufactured within an established standard time and ensure timely delivery of quality goods with minimum defects to serve sales demand at the right cost.

2)Monitor and execute the operational activities, cleaning and disinfection, and changeover of equipment in critical areas such as Dispensing, Mixing, Sterilization, Component Preparation and Filling.

3)To assist team leader on overall SVI activities, manpower management (e.g. overtime works) and material management (raw material, packaging material & consumable items) to ensure the smoothness of overall daily activities.

4) To execute the monthly & weekly SVI schedule/plan activities and ensure the daily output to achieve the daily targeted output.

5)Monitor and ensure discipline, attendance, and working hours of all subordinates/ process technician are according to company policies. To report/ notify the team leader accordingly for next action.

6)To ensure timely update documentation including but not limited to SOPs, logbooks, Forms and Batch Manufacturing Record (BMR).

7)Ensure accurate and timely data ready for entry into SAP systems to support material traceability, and overall process control.

8)Execution of manufacturing processes in accordance with approved Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), and other controlled documents.

9)Perform preliminary verification and review of but not limited to logbooks, Forms and Batch Manufacturing Record (BMR) to ensure data integrity and completeness.

10)Assist on timely closure of deviations, CAPAs, change controls and audit findings related to production operations when required.

11)Assist for troubleshooting, equipment failure recovery, and abnormal situations, subsequently reporting to the immediate superior, Executive/Head of Section.

12)Provide support to QC, Engineering and Technical Services on any inspection/sampling, preventive maintenance, equipment calibration, and validation support. Ensure to notify the respective team leader/ superior prior to the coordination and assistance.

13)Ensure cleanroom aseptic behavior, hygiene practices, and gowning compliance are strictly followed by all production personnel.

14)Oversee and suggest competency development of Technicians by organizing structured on-the-job training (OJT) and refresher sessions.

15)Assist on the compilation and report of daily production target, shift performance, and equipment downtime trends to the superior.

16)Assist on line readiness and act as line SME (subject matter expert) during internal and external audits, regulatory inspections, or validation protocol reviews.

17) Ensure subordinates/ process technician on the proper use and availability of PPE, appropriate tools, and consumable materials at required process area.

18) To uptake Production Team Leader responsibilities if required due to absence or as and when required.

19) To uptake the responsibilities of Insulin / PFS Biopharma section in the absence of respective process leader or as and when required.

Supervisor:

1.To assist the Head of Section/Executive, supervise and monitor the whole Insulin Biopharma activities to ensure products are manufactured within an established standard time and ensure timely delivery of quality goods with minimum defects to serve sales demand at the right cost.

2.Supervise the operation, cleaning, and changeover of equipment in critical areas such as Dispensing, Mixing/Formulation, Sterilization, Component Preparation and Filling.

3.To coordinate overall Insulin Biopharma activities, manpower management (e.g. overtime works) and material management (raw material, packaging material & consumable items) to ensure the smoothness of overall daily activities.

4.To implement monthly & weekly Insulin Biopharma schedule/plan activities and monitor the daily output to ensure daily targeted output are achieved and monitor manpower requirement for the month.

5.Monitor and ensure discipline, attendance, and working hours of all subordinates are according to company policies.

6.To check, review and timely update documentation including but not limited to SOPs, logbooks, Forms and Batch Manufacturing Record (BMR).

7.Ensure accurate and timely data entry into SAP systems to support material traceability, and overall process control.

8.Oversee the execution of manufacturing processes in accordance with approved Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), and other controlled documents.

9.Perform verification and final review of but not limited to logbooks, Forms and Batch Manufacturing Record (BMR) to ensure data integrity and completeness.

10.Assist timely closure of deviations, CAPAs, change controls and audit findings related to production operations using TrackWise.

11.Provide first-level support and decision-making for troubleshooting, equipment failure recovery, and abnormal situations, subsequently reporting to the immediate superior, Executive/Head of Section.

12.Coordinate and liaise with QC, Engineering and Technical Services on any inspection/sampling, preventive maintenance, equipment calibration, and validation support.

13.Ensure cleanroom aseptic behavior, hygiene practices, and gowning compliance are strictly followed by all production personnel.

14.Oversee and suggest competency development of Process Leaders and Technicians by organizing structured on-the-job training (OJT) and refresher sessions.

15.Provide and assist with relevant training as per but not limited to training need matrices (TNM) in compliance with Quality Management System requirements.

16.Compile and report daily production target, shift performance, and equipment downtime trends to the Head of Section/Executive.

17.Provide and support line readiness and act as line SME (subject matter expert) during internal and external audits, regulatory inspections or validation protocol reviews.

17.Ensure proper use and availability of PPE, appropriate tools, and consumable materials at required process area.

18.To uptake Executive/Head of Section responsibilities if required due to absence or as and when required.

19.To uptake the responsibilities of SVI / PFS Biopharma section in the absence of respective Supervisor or as and when required.

Job Types: Full-time, Contract

Pay: RM1,950.00 - RM3,075.00 per month

Benefits:

• Free parking
• Health insurance
• Maternity leave
• Meal allowance
• Professional development

Education:

• Diploma/Advanced Diploma (Preferred)

Experience:

• Training & Development: 2 years (Preferred)

Work Location: In person