Operator - Assistant / Associate - Sterile Manufacturing @ Amneal

We are looking for competent, dynamic and motivated candidates for Manufacturing- QMS Injectable department for Amneal Pharmaceutical Pvt. Ltd (Injectable units, SEZ-Matoda Plant,Ahmedabad)Job DescriptionKey Responsibilities:Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility.Responsible for...

Amneal Pharma Walk-in Drive @ Pharma-SEZ, Matoda, Ahmedabad, (Gujrat) for Production department (Injectable/ Sterile) on 2nd November 2025 (Sunday)We are looking for suitable candidates for injectable/ sterile manufacturing units for Ahmedabad location.Interview Details:Date: 2nd November, 2025 (Sunday),Time: 09:00 AM to 05:00 PMInterview Venue :Amneal...

Key Responsibilities Strategic Leadership & Technical OversightDrive the MSTG strategy for injectable manufacturing, aligning with corporate goals and regulatory expectations.Lead cross-functional teams in the design, development, and optimization of manufacturing processes.Provide technical leadership during product lifecycle stages including development,...

We are Hiring | Assistant Manager/ Deputy Manager - HVAC Process Engineer (SME)Job overview:We are looking for an Assistant Manager/ Deputy Manager - HVAC Engineer (SME) with strong experience in pharmaceutical HVAC system design, execution, and validation.The role involves supporting greenfield and brownfield pharma projects while ensuring compliance with...

Responsible for document management like BMRs, BPRs, master SOPs etc..Responsible for preparation & review of the master documents of production.Responsible to ensure UAF working in area.Responsible for the handling of change control, deviations, investigation & CAPA, etc.Responsible to check that all the records and logbooks related to manufacturing,...

Key Responsibilities:1. Process Design & OptimizationLead the design, development, troubleshooting and optimization of aseptic filling processes for vials, PFS, bags, and cartridges.Review and provide support to validate process parameters (e.g., filling speed, accuracy, container closure integrity) ensuring product quality and sterility...

WL Protocol Execution at each siteReview of outcome of protocol-based studies as outlined in the FDA commitment.Protocol based retrospective review of investigations (deviations, OOS and OOAL) of product batches within shelf life.Protocol based Retrospective review of investigations related to market complaints.Protocol for Material system assessment and...

Job Responsibility:Supervision of manufacturing, processing, packaging and holding of drug product as per define and approved procedures for stability batches and commercial batches.Maintaining the area and equipment in orderly manner as per cGMP requirements in a good state of repair and sanitized condition.To perform online documentation with respect to...

Job DescriptionTo work in collaboration with US team members to create the highest quality documents and timely delivery of outputs consistently.Prepare and review PPQP, PPQR, PSP, PSR, CPVP, BBHS, regulatory modules (for submission/validation batches).Prepare and review Cleaning Validation documents (Matrix, CVP, CVSR & CVR's) in addition to timely...

Plan, execute, and monitor capital projects for pharma manufacturing facilities (API/Formulations).Oversee design, installation, and commissioning of utilities, HVAC, cleanrooms, and automation systems.Ensure compliance with cGMP, EHS, and global regulatory standards throughout project lifecycle.Prepare project budgets, timelines, and resource allocation...