Production Officer

Production Officer,Production Planning,Man power Handling , GMP,BMR,SOP,Process COsmetic Healthcare Industry. Silvassa location1)IPQA (3.0lac p..a)2)Production Officer (2 lac to 4.0lac p.a.) BSC Chemistry & B.pharma

Role & responsibilities Production Officer - Compression Preferred candidate profile Exposure of Fette, Sejong, Legacy, Korsch, Cadmach or any other machine having Automatic Weight Control / Compaction Force Control, Handling of QMS Work (CCP,CAPA, Deviation, Investigation & Documentation)

Title: Senior Officer - Quality ControlDate: Sep 25, 2025Location: Dadra - Quality ControlCompany: Sun Pharmaceutical Industries LtdJob Summary:The QC Analyst is responsible for performing analytical testing of raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with USFDA regulations, cGMP standards, and internal...

Company DescriptionNavneet Education Limited, established by the Gala Family in 1959, is a prominent educational content provider in both print and digital mediums. The company also manufactures scholastic paper stationery and publishes general and children's books. Navneet is a leading brand for educational products in India, with a significant market share...

Roles and ResponsibilitiesImplement QA/QC Policy of the company.To ensure that all RM/PM received adhere to the standard specification.To ensure that all finished goods manufactured in the factory adhere to the standard product specification.To ensure that all the operation/process is as per formulation and standard.To conduct finished product analysis as...

Job Title: Packing Supervisor – OSD (USFDA Approved Plant)Job Location: DadraJob SummaryThe Packing Supervisor will oversee and manage the packaging operations of oral solid dosage pharmaceutical products in compliance with USFDA, cGMP, and company standards. This role ensures timely execution of packing activities, adherence to quality and safety norms,...

Role & responsibilitiesDocumentation Issuance & Control Issue Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and logbooks to production as per SOP. Maintain master documents for BMR, BPR, SOPs, and other controlled documents with proper version control. Implement and maintain document control systems as per GDP and cGMP requirements.Batch...

Conduct FPA & in-process quality checksMaintain daily MIS reports for quality trackingEnsure documentation and production approvalsAssist in RCA & support CAPA implementationMaintain inspection recordsSupport internal audits and document reviews

Job SummaryThe QC Analyst is responsible for performing analytical testing of raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with USFDA regulations, cGMP standards, and internal specifications. This role is critical in maintaining product quality, safety, and efficacy.Key ResponsibilitiesAnalytical...

Role & responsibilitiesMicrobiological Analysis Conduct microbial limit test, sterility test, endotoxin testing, and bioburden analysis on raw materials, in-process, and finished products. Perform water testing for purified water and potable water systems as per pharmacopeial standards. Conduct environmental monitoring of cleanrooms and controlled areas,...