3406 Job openings found

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, ...

We have an urgent opening for the position of Asst. Manager / Manager – Quality Assurance Auditor for a leading producer of specialty chemicals for the Ambernath location. Designation: Asst. Manager / Manager – Quality Assurance Auditor Job Location: Ambarnath Education: M.Sc./ B.Sc. with any Specialization Certificate in Pharma Audit  Skills: Familiar with applicable and appropriate regional ...

Position:          Assist. Manager -QA Location:         Silvassa Experience:     10- 15 Years Industries:      Pharma Formulation Responsibilities: QMS,Cleaning validation, Process validation,Technology Transfer,SOP Prepration,Qualification,Audit Compliance,Media Fill Validation ISO/GMP Systems: Maintenance and continuous improvements in procedures and documentation, certification and compliance. Customer registrations, Handling customer audits and complaints, CAPAs and closures. FG/RM/PM specifications, Test ...

Responsible for Planning of Pharma  Machines(Injectable dry powder and liquid filling) & All types  of Machines (washing,sealing,capping & labeling). Maintaining good quality of machine and components as per  company standards Preparation of costing sheets for individual machines and for projects for cost benefits and for healthy negotiation with vendors to get the higher discounts on existing ...

JOB PURPOSE     Implement and monitor packing activities adhering to Regulatory, GQS and HSE requirement with proper utilization of resources, maintaining consistent good quality of product to meet with the customers’ requirements and fulfill the organization’s objectives, living Group’s Values and Code of Ethics.   REQUIREMENTS Education / Experience Graduate in Pharmacy 3 to 5 years ...

Position:          QA Manager  Location:         Vapi Experience:     10- 15 Years Industries:       Pharma API Responsibilities: ISO/GMP Systems: Maintenance and continuous improvements in procedures and documentation, certification and compliance. Customer registrations, Handling customer audits and complaints, CAPAs and closures. FG/RM/PM specifications, Test plans and Customer order review Vendor qualifications, audits and ratings. USFDA, ...

Job Description: He will report to the Technical Manager and will be a key member of the team at head office. He will assist the Technical Manager in all routine tasks related to factory/technical issues of the entire formulations business. Coordinate and monitor production at own factory and other third party factories ...

Position:          Sr. Executive/Asst. Manager -QA Location:         Vapi Experience:     4- 8 Years Industries:      Medical Device Responsibilities: Should have experience in Medical Device Coordinate with Certification body for Certification / Surveillance Audit. Conduct Internal Quality audit as per define timeline. Document and Data control by periodic review of SOPs, Formats. Develop, ...

Position:           Maintenance Engineer Location:          Thumb near by Vapi Experience:       1-2  Years Industries:        Metal   Responsibilities: Carry out routine maintenance work Preventive Plan Maintenance Basic knowledge of Transformer, Air Compressor, Lift & D.G. Troubleshooting skills & root cause analysis Advanced knowledge of mechanical & electrical. Responsible for installation & Maintenance of industrial Equipment's. Understanding ...

 Position:          QA Executive Location:          Silvassa Experience:      7 -10 Years Industries:       Pharma Formulation    Responsibilities:         Preparing and implementing quality assurance policies and procedures. Performing routine inspections and quality tests. Identifying and resolving workflow and production issues. Ensuring that standards and safety regulations are observed. Addressing and discussing issues and proposed solutions with superiors. Documenting quality assurance ...