Hetero

We are seeking a knowledgeable and dedicated IT Support professional to join our dynamic team. The ideal candidate will possess a thorough understanding of esse

Manufacturing Oversight Monitor manufacturing activities to ensure compliance with cGMP and approved procedures. Perform line clearance before the start of prod

Key Responsibilities: Execute API manufacturing activities as per approved Batch Manufacturing Records (BMRs), SOPs, and cGMP guidelines. Operate and monitor pr

Key Responsibilities:Oversee In-Process Quality Assurance (IPQA) activities during API manufacturing operations. Ensure compliance with cGMP, SOPs, and regulato

Designation: Manager ? QA QMS Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm Experience: 8?15 Years Key Responsibilities: Manage and oversee Quality Management

Role & responsibilities Prepare and compile regulatory dossiers for submissions to the US, EU, WHO, and other global markets. Support the preparation, review, and maintenance of Drug Master Files (DMFs). Review technical documents such as specifications, manufacturing process documents, and spike st

1. Follow shift schedule and production schedule as per process requirement. 2. Handling of plasma collection, sanitization, washing, cutting, pooling and thawi

-To perform operation, cleaning and changeover of the equipment like the Vial Washing Machine, Vial Depyrogenation tunnel, Vial Filling & Stoppering Machine, Vi

Job Description: Junior Technician Role: Junior Technician (Fitter / Electrician) Department: Engineering Maintenance (API) Experience: 01 Year (Fresher) Qualif

Role & responsibilities: Lead plant Safety & Environment operations and ensure compliance with applicable statutory and regulatory requirements. Develop, implem

Hiring for Sr Officer / Executive for Purchase Raw Materials Department : Purchase Raw Materials Position: Sr. Officer / Executive Experience: 25 Years Key Resp

1.Responsible to follow GLP practices in QC RM/PM testing laboratory of Hetero Plasma Sciences Private Limited, Kothur. 2.Responsible for calibration of analytical balance, pH meter and calibration. 3.Responsible for preparation of reagent solutions and volumetric solutions. 4.Monitoring area cleani

Verification of all material bills and processing inMIRO Verification of all service bills and processing inMIRO Verification and parking of employee reimbursement,travel expenses in FI module Review of vendor employee advances and clearing. Accounting ofmonth end entries like. salaries, PF, PT, ESI

Job Summary We are seeking a highly motivated Project Management Professional with 36 years of experience in the API/CDMO pharmaceutical industry. The ideal candidate should have exposure to Technology Transfer (TSD), Production, Quality Assurance (QA), or Quality Control (QC) and be capable of mana

The candidate will be responsible for implementing safety practices, environmental compliance, hazard control, and statutory requirements to ensure safe plant o

We are looking for a highly skilled and experienced Assistant Manager to join our team in the Regulatory Affairs department. The ideal candidate will have 2-5 years of experience in regulatory affairs, preferably in the pharmaceutical industry. Roles and Responsibility Compile and submit USDMF and E

We are looking for a highly skilled and experienced Assistant Manager to join our team in the Regulatory Affairs department. The ideal candidate will have 2-5 years of experience in regulatory affairs, preferably in the pharmaceutical industry. Roles and Responsibility Compile and submit USDMF and E

Job Description: Responsible for regulatory submissions and lifecycle management of API products for the China market . Prepare, compile, review, and submit China DMF dossiers in line with NMPA regulatory requirements. Handle new registrations, amendments, renewals, and annual maintenance of regulat

Job Description: Responsible for regulatory submissions and lifecycle management of API products for the China market . Prepare, compile, review, and submit China DMF dossiers in line with NMPA regulatory requirements. Handle new registrations, amendments, renewals, and annual maintenance of regulat

Majority of experience should be in Process safety and with minor in General Safety. Responsible to lead the cultural transformation on Process Safety management in sites. Responsible to review the new projects, new processes, modifications in point of change management before initiation of change.