Career Opportunities: ASSISTANT MANAGER (6834)
Job Description Print Preview
Department Details
Role Summary
Generic Formulations - Supervisor Packing
Key Responsibilities
• Responsible for Packing of solid oral dosage forms.
• Candidate must have faced major regulatory audits (like USFDA, MHRA etc.)
• Preparation and updatation standard procedures (SOP/EOP/IOP/SCP) for different activities, as per regulatory requirements.
• Team Development through technical and procedural training.
• To ensure the compliance of standard procedures by the team.
• Implementation of GMP norms in daily production activities.
• Assure the real time data capturing and other GDP principles by the team at production.
• To ensure online up-date of Packing records.
• Execution of Equipment Qualification.
• Equipment upkeeping through on time completion of machine maintenance in co-ordination with Engineering persons.
• Candidate shall be responsible to maintain change part inventory at minimum level.
• Person shall have responsibility to handle the Quality management system (QMS) activities in Trackwise.
• Candidate should have SAP knowledge and shall be responsible to update the production related activities in SAP.
• Responsible for execution and completion of daily production plan.
• Should have good communication skill to co-ordinate with internal stake holders like Warehouse, QA, QC, Maintenance to meet daily production plans.
• Candidate shall be responsible for deliverance of exhibit/process validation batches as per committed timeline.
• Preparation and updatation of Batch Packing records considering the regulatory requirements.
• To update reporting manager about availability of spares and consumables on shop floor.
• To prioritize and practice the safety principles and company policies in factory premises.
• To work upon Operational Excellence projects.
Educational Qualifications
Required Education Qualification: B.Pharma
Required Experience: 4 - 10 years
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Department Details
Role Summary
Generic Formulations - Supervisor Packing
Key Responsibilities
• Responsible for Packing of solid oral dosage forms.
• Candidate must have faced major regulatory audits (like USFDA, MHRA etc.)
• Preparation and updatation standard procedures (SOP/EOP/IOP/SCP) for different activities, as per regulatory requirements.
• Team Development through technical and procedural training.
• To ensure the compliance of standard procedures by the team.
• Implementation of GMP norms in daily production activities.
• Assure the real time data capturing and other GDP principles by the team at production.
• To ensure online up-date of Packing records.
• Execution of Equipment Qualification.
• Equipment upkeeping through on time completion of machine maintenance in co-ordination with Engineering persons.
• Candidate shall be responsible to maintain change part inventory at minimum level.
• Person shall have responsibility to handle the Quality management system (QMS) activities in Trackwise.
• Candidate should have SAP knowledge and shall be responsible to update the production related activities in SAP.
• Responsible for execution and completion of daily production plan.
• Should have good communication skill to co-ordinate with internal stake holders like Warehouse, QA, QC, Maintenance to meet daily production plans.
• Candidate shall be responsible for deliverance of exhibit/process validation batches as per committed timeline.
• Preparation and updatation of Batch Packing records considering the regulatory requirements.
• To update reporting manager about availability of spares and consumables on shop floor.
• To prioritize and practice the safety principles and company policies in factory premises.
• To work upon Operational Excellence projects.
Educational Qualifications
Required Education Qualification: B.Pharma
Required Experience: 4 - 10 years
-
- The job has been sent to
Department Details
Role Summary
Generic Formulations - Supervisor Packing
Key Responsibilities
• Responsible for Packing of solid oral dosage forms.
• Candidate must have faced major regulatory audits (like USFDA, MHRA etc.)
• Preparation and updatation standard procedures (SOP/EOP/IOP/SCP) for different activities, as per regulatory requirements.
• Team Development through technical and procedural training.
• To ensure the compliance of standard procedures by the team.
• Implementation of GMP norms in daily production activities.
• Assure the real time data capturing and other GDP principles by the team at production.
• To ensure online up-date of Packing records.
• Execution of Equipment Qualification.
• Equipment upkeeping through on time completion of machine maintenance in co-ordination with Engineering persons.
• Candidate shall be responsible to maintain change part inventory at minimum level.
• Person shall have responsibility to handle the Quality management system (QMS) activities in Trackwise.
• Candidate should have SAP knowledge and shall be responsible to update the production related activities in SAP.
• Responsible for execution and completion of daily production plan.
• Should have good communication skill to co-ordinate with internal stake holders like Warehouse, QA, QC, Maintenance to meet daily production plans.
• Candidate shall be responsible for deliverance of exhibit/process validation batches as per committed timeline.
• Preparation and updatation of Batch Packing records considering the regulatory requirements.
• To update reporting manager about availability of spares and consumables on shop floor.
• To prioritize and practice the safety principles and company policies in factory premises.
• To work upon Operational Excellence projects.
Educational Qualifications
Required Education Qualification: B.Pharma
Required Experience: 4 - 10 years
