?ENSURE ALL TRAINING ON EQUIPMENT, PROCESSES, AND FACILITY AND
SAFETY PROCEDURES ARE MAINTAINED AND UP TO DATE AT ALL
TIMES.?PERFORM DAY-TO-DAY MANUFACTURING AND CLEANING ACTIVITIES TO
MEET SCHEDULES WHILE MAINTAINING A HIGH LEVEL OF GMP COMPLIANCE.?TO
AID WITH TROUBLESHOOTING AND RESOLVING OPERATIONAL PROBLEMS DURING
PACKAGING.?ENSURE ALL DOCUMENTATION IS COMPLETED TO THE REQUIRED
STANDARD AND WITHIN THE SPECIFIED TIMELINES.?REVIEW BATCH RECORDS
AND OTHER MANUFACTURING PROCESS RECORDS AS REQUIRED.?ROUTINELY DRAFT
AND REVISE STANDARD OPERATING PROCEDURES AND MASTER BATCH
RECORDS.?TO AID IN DEVIATION INVESTIGATIONS AND CLOSURES.?SUPPORT
CONTINUOUS IMPROVEMENT INITIATIVES BY IDENTIFYING AREAS NEEDING
IMPROVEMENT, RECOMMENDING STRATEGIES FOR IMPROVEMENT, AND IMPLEMENTING
THOSE STRATEGIES ONCE APPROVED.?MAINTAIN A HIGH, AND CONTINUOUSLY
IMPROVING, LEVEL OF GMP COMPLIANCE TO ENSURE PATIENT SAFETY AND TO
MINIMIZE RISK TO THE COMPANY BUSINESS. ?SUPPORT REGULATORY LICENSURE
ACTIVITIES, INCLUDING AGENCY INSPECTIONS. ?REPORT TO AREA SUPERVISOR
ON A REGULAR BASIS ON LINE PERFORMANCE AND REPORT ANY ISSUES THAT NEED
TO BE RESOLVED.?TO TRAIN AND BE CROSS FUNCTIONAL ACROSS ALL
MANUFACTURING AREAS OF THE PACKAGING AND WAREHOUSE FACILITY.?TO
PERFORM ANY OTHER TASK OR DUTIES AS ASSIGNED BY AREA SUPERVISOR.
REQUIREMENTS
EDUCATION: ?THIRD LEVEL QUALIFICATION IN A SCIENTIFIC OR ENGINEERING
DISCIPLINE OR EQUIVALENT EXPERIENCE WOULD BE DESIRABLE. SKILLS:
?**APPLY ON THE WEBSITE** YEARS? EXPERIENCE IN PACKAGING
OPERATIONS IN A GMP ENVIRONMENT.?MUST BE ABLE TO WORK WITHIN AND
ADAPT TO COMPLEX ELECTRONIC SYSTEMS SUCH AS SAP.?EXPERIENCE WITH
WAREHOUSE EQUIPMENT AND SYSTEMS PREFERRED.?SHOULD BE KNOWLEDGEABLE
OF REGULATORY AND GMP REQUIREMENTS.JOB DESCRIPTION
?ENSURE ALL TRAINING ON EQUIPMENT, PROCESSES, AND FACILITY AND
SAFETY PROCEDURES ARE MAINTAINED AND UP TO DATE AT ALL
TIMES.?PERFORM DAY-TO-DAY MANUFACTURING AND CLEANING ACTIVITIES TO
MEET SCHEDULES WHILE MAINTAINING A HIGH LEVEL OF GMP COMPLIANCE.?TO
AID WITH TROUBLESHOOTING AND RESOLVING OPERATIONAL PROBLEMS DURING
PACKAGING.?ENSURE ALL DOCUMENTATION IS COMPLETED TO THE REQUIRED
STANDARD AND WITHIN THE SPECIFIED TIMELINES.?REVIEW BATCH RECORDS
AND OTHER MANUFACTURING PROCESS RECORDS AS REQUIRED.?ROUTINELY DRAFT
AND REVISE STANDARD OPERATING PROCEDURES AND MASTER BATCH
RECORDS.?TO AID IN DEVIATION INVESTIGATIONS AND CLOSURES.?SUPPORT
CONTINUOUS IMPROVEMENT INITIATIVES BY IDENTIFYING AREAS NEEDING
IMPROVEMENT, RECOMMENDING STRATEGIES FOR IMPROVEMENT, AND IMPLEMENTING
THOSE STRATEGIES ONCE APPROVED.?MAINTAIN A HIGH, AND CONTINUOUSLY
IMPROVING, LEVEL OF GMP COMPLIANCE TO ENSURE PATIENT SAFETY AND TO
MINIMIZE RISK TO THE COMPANY BUSINESS. ?SUPPORT REGULATORY LICENSURE
ACTIVITIES, INCLUDING AGENCY INSPECTIONS. ?REPORT TO AREA SUPERVISOR
ON A REGULAR BASIS ON LINE PERFORMANCE AND REPORT ANY ISSUES THAT NEED
TO BE RESOLVED.?TO TRAIN AND BE CROSS FUNCTIONAL ACROSS ALL
MANUFACTURING AREAS OF THE PACKAGING AND WAREHOUSE FACILITY.?TO
PERFORM ANY OTHER TASK OR DUTIES AS ASSIGNED BY AREA SUPERVISOR.
REQUIREMENTS
EDUCATION: ?THIRD LEVEL QUALIFICATION IN A SCIENTIFIC OR ENGINEERING
DISCIPLINE OR EQUIVALENT EXPERIENCE WOULD BE DESIRABLE. SKILLS:
?**APPLY ON THE WEBSITE** YEARS? EXPERIENCE IN PACKAGING
OPERATIONS IN A GMP ENVIRONMENT.?MUST BE ABLE TO WORK WITHIN AND
ADAPT TO COMPLEX ELECTRONIC SYSTEMS SUCH AS SAP.?EXPERIENCE WITH
WAREHOUSE EQUIPMENT AND SYSTEMS PREFERRED.?SHOULD BE KNOWLEDGEABLE
OF REGULATORY AND GMP REQUIREMENTS.
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Type: Permanent
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Category: Others
