Compliance to cGMP and other regulatory requirement. To monitor the daily packing activates in primary packing in with compliance of cGMP norms. To execute packing inputs as per shift plan in Advanced & achieve it. Ensure compliance of the online Documents during packaging process. To ensure the
Shift Supervisor jobs in Dholka
42 shift supervisor opportunities in Dholka updated today
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· Page 1 / 3Job Description: • Compliance to cGMP and other regulatory requirement. • To monitor the daily packing activates in primary packing in with compliance of cGMP norms. • To execute packing inputs as per shift plan in Advanced & achieve it. • Ensure compliance of the online Documents during packagi
Major purpose of the Job: -Reviewing overall data management activities for assigned studies. RESPONSIBILITY: Clinical Data Management: -Preparation of DMP (Data Management Plan), Data Validation Plan (DVP) and Self-Evident Correction Convention (SECC). -Preparing & Updating of SOPs. -Ensuring S
To ensure achievement of planned productivity with quality compliance in respective shift. Work allocation & proper utilization of men & machine. Co-ordination with Tablet Mfg./Secondary packing/QA/QC/stores supply chain/BSR. To ensure availability of required packing material, Change Parts&
To meet agreed production targets with due compliance to regulatory norms. To ensure proper utilization and productivity of manpower and machines. To ensure all records/documents of department are maintained in compliance to regulatory. To ensure optimization of resources and reduction of waste/reje
Job Description: JOB RESPONSIBILITIES "Purification of recombinant vaccine candidates. • pH and conductivity meter calibration and operation • Stock buffers and working buffer preparation • Column packing for purification of vaccine projects • Column cleaning CIP, storage and maintenance • Protein c
Job Description: Major purpose of the Job: -Reviewing overall data management activities for assigned studies. RESPONSIBILITY: Clinical Data Management: -Preparation of DMP (Data Management Plan), Data Validation Plan (DVP) and Self-Evident Correction Convention (SECC). -Preparing & Updating of
Job Description: • To ensure achievement of planned productivity with quality compliance in respective shift. • Work allocation & proper utilization of men & machine. • Co-ordination with Tablet Mfg./Secondary packing/QA/QC/stores supply chain/BSR. • To ensure availability of required packin
Job Description: • To meet agreed production targets with due compliance to regulatory norms. • To ensure proper utilization and productivity of manpower and machines. • To ensure all records/documents of department are maintained in compliance to regulatory. • To ensure optimization of resources an
Job Description: 1. Planning and execution of Validation, Qualification, Re-Qualification and Re-Validation activities pertaining to Manufacturing facility at Dholka site in line with the cGMP requirements of national and international regulatory authorities. 2. To Perform Vendor Management Activity
Job Description: To assure Quality and cGMP compliance of the products being manufactured and Packed for Cephalosporin Block. • To review MMD-I / BPR and release of the batches for further processing stage like Granulation, compression, coating, inspection, filling and packing. • To ensure IPQA func
Job Description: • Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory. • To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP. • To follow safety Procedure in Microbiology laboratory (Main Pharma
Job Description: Manage day-to-day operations of the pharmaceutical stores and warehouse. Ensure proper receipt of raw materials, packaging materials, finished goods, engineering materials, and consumables. Verify incoming materials against purchase orders, delivery documents, specifications, quanti
Job Description: 1. Process Improvement • Achieve measurable improvements in manufacturing cycle times or process, online documentation and productivity. • Implement continuous improvement initiatives to enhance operational performance. 2. Capacity Utilization • Achieve alignment between production
Job Description: "• Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory. • To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP. • To follow safety Procedure in Microbiology laboratory (Main Pharm
• Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory. • To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP. • To follow safety Procedure in Microbiology laboratory (Main Pharma-QC) • To attend
1. Process Improvement • Achieve measurable improvements in manufacturing cycle times or process, online documentation and productivity. Implement continuous improvement initiatives to enhance operational performance. 2. Capacity Utilization • Achieve alignment between production schedules, inventor
"• Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory. To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP. To follow safety Procedure in Microbiology laboratory (Main Pharma-QC) • To attend the
Job Description: Principal Tasks & Responsibilities New & Renewal Dossier Filings: Prepares, reviews, and submits new and renewal registration dossiers to support SBU targets across specified countries. MoH & Customer Query Resolution: Drafts and shares pre-registration responses to cust
Description Manage day-to-day operations of the pharmaceutical stores and warehouse. Ensure proper receipt of raw materials, packaging materials, finished goods, engineering materials, and consumables. Verify incoming materials against purchase orders, delivery documents, specifications, quantity, a
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Team Leadership Lead, coach, and develop a team of transition team members. Allocate work, monitor progress, and ensure timely completion of deliverables. Review work quality, resolve escalations, and drive process improvements. Provide regular updates to management on transition status and risks. A
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Estimated salary for Shift Supervisor in Dholka
₹5,40,000 – ₹8,60,000/year
Estimation confidence: Low
Estimate based on market data for Dholka. Actual salaries may vary depending on experience, company, and area.
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