1 Opening(s)
1.0 Year(s) To 7.0 Year(s)
1.80 LPA TO 2.40 LPA
Minimum 2 to 5 Years Experience
Must have experience in operating Coating machines
Experience in machine setting and operation.
Records and maintains the production batch record during the coating operation.
Observes machine gauges and equipment calibration status and reports any deviations to Superiors.
Operates auxiliary equipment used in coating pans and Spray Gun setup.
Cleans and ...
3 Opening(s)
4.0 Year(s) To 6.0 Year(s)
3.50 LPA TO 4.00 LPA
Hiring for Starch powder, liquid Glucose Manufacturing Industry
Position:- Production Assistant Manager & Supervisor
(Products - liquid Glucose, Sorbital, DMH, DAH, M alto Destine)
Education: - B.E chemical / Bcs Chemistry
Experience: - Min 2 to 8 Years in a chemical factory, Food Industry, and Pharma Industry
Job Description:
Plan and execute production plan to meet marketing requirements following ...
4 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.40 LPA TO 5.00 LPA
Hiring for API / Pilot Plant
Designation: Production Executive/ Sr. Executive
Qualification: B.Sc. / M.Sc chemistry
Designation: Executive/ Sr. Executive.
Experience: Minimum 2 to 8 years in must have experience in API Production / Pilot Plant
Equipment handled -: Reactors, Centrifuge, Dryers, Sifter, and Blender etc.
Job Profile:
Responsible For All Activity in Plant during Shift as an Officer.
Ensuring that ...
1 Opening(s)
1.0 Year(s) To 7.0 Year(s)
1.80 LPA TO 2.40 LPA
Minimum 2 to 5 Years Experience
Must have experience in operating Coating machines
Experience in machine setting and operation.
Records and maintains the production batch record during the coating operation.
Observes machine gauges and equipment calibration status and reports any deviations to Superiors.
Operates auxiliary equipment used in coating pans and Spray Gun setup.
Cleans and ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 3.00 LPA
1.Quality Control functions in Pharmaceutical manufacturing facility.
2.Testing and analysis of various raw materials and finished products.
3.Must be versatile with documentation as per GMP (Good Manufacturing Practice) including preparation of BMR, Analytical documents and other relevant statutory procedures.
4. Should have hands-on experience with statutory compliances, analytical instruments, with good knowledge of ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
6.00 LPA TO 10.00 LPA
Leading and Management of IPQA team.Performing IPQA activity (Line clearance, in-process checks, sampling, etc.) at shop floor for Dispensing, Manufacturing, and Packing area.Review of executed Batch Processing Records and related cGMP documents for the on-time release of the batch.Preparation of SOP for execution on shop floor IPQA related activities.
Review of ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
2.10 LPA TO 3.60 LPA
Receiving Monthly & daily Production plan from Production Manager.
Manufacturing of batch as per MBR.
Temperature & Relative Humidity monitoring in manufacturing area.
Maintaining logbooks(General cleaning logbook,Equipment calibration & cleaning logbook,).
Preparation of daily production & manpower Record.
Online the Batch Manufacturing Record (BMR).
In process checks of all stages of manufacturing & packing of Tablet, ...
8 Opening(s)
0 To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Department - QA
Job Locaion - ambernath
Willingness should be there to work in all shifts
Job Description
Experience in issuing of line clearance at every step of Batch Manufacturing
Hands on performing In-process quality assurance checks for Tablets, Capsules and Intermediates.
Stability Sample Handling as well as Stability Chamber.
Monitoring and Executing Process Validation and Sampling of the same.
Carry out In-house Calibration and External Calibration of Balance, Instrument, Equipments, LAF and HVAC validation.
Periodic checking of Retention Sample and Handling of the same.
Documentation of Records.
BMR and BPR Preparation and reviewing.
Carry out Destruction Activities for Rejected and Expired Raw and Packing Materials.
Preparation of PQR & APQR.
1 Opening(s)
0 To 2.0 Year(s)
0.00 LPA TO 2.40 LPA
Executing production activities as per approved Batch Manufacturing Records (BMR) and Standard Operating Procedures (SOP).
Monitoring production parameters such as temperature, humidity, and pressure during manufacturing.
Maintaining accurate records, including logbooks, BMR, and cleaning checklists.
Conducting in-process checks to ensure quality standards are met at each stage of production.
Coordinating with Quality Assurance (QA), ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
3.60 LPA TO 5.40 LPA
Job Description:1. Responsible for Overall QA activities & to look after QMS compliance in accordance with ISO 13485/cGMP.2. Preparation & Up-gradation of SOP, Specifications3. Maintain the Records of BMR, BPR, Batch Inspection Documents4. Maintaining Document & Record Control5. Preparation & Up-gradation of Routine Validation Protocol & Reports.6. Handling CAPA, Non- ...