74 Job openings found

Qualification: Graduate and Material management diploma can be preferable.Experience: min 7 to 12 years experience in overall store activities in chemical industry.Work location: Nerul Plant location in MumbaiReporting to Stores manager Job Responsibilities:➢ Ensure availability of required raw materials by continuous follow up with Purchase as per production plan so that ...

Responsibility:  To maintain the entire documentation as per cGMP and ISO 9001:2015 on daily and fortnightly basis. To supervise the Shift Inspector and Assembly Supervisor. To prepare necessary documentations for new product development trials. Responsible for auditing OPC and preparing the related documents. Responsible to take the trials of new ...

Sr. Manager- Quality Assurance (QA QC)   Job Responsibilities?:-  Planning and execution of daily QA, QC operation activities for production in Injectable section to smooth Functioning work culture.  To prepare and review the   SOPs of QA QC departments. Ensure qualification/ validation status of equipment’s   QA, QC of Internal and external Manufacturing as per SOP.  Experience of handling ...

Technical Function – Operation Of Distillation / MEE/ Filtration Area Responsibility – Recovery Plant 1. Verification of Distillation / Verification MEE/ Verification Filtration 2. Verification of Document Process 3. Plant document as per CGMP.     Technical Function – Operation Of Distillation / MEE/ Filtration Area Responsibility – Recovery Plant 1. Verification of Distillation / ...

To understand, communicate and prepare a system to meet the desired production of each product as per the plan agreed by SCM team.   To manufacture all products of high quality by complying with CGMP and safety systems at Udaipur Plants.   To Plan and set production targets and ensure achieving the same for ...

Position:          Quality Head Location:         Bhopal Experience:     18 - 25 Years Industries:       Pharma  Responsibilities: Lead the QA/QC functions for biological and insulin product lines, ensuring compliance with global regulatory standards (FDA, EMA, etc.) and cGMP requirements. Develop, implement, and maintain robust quality management systems, policies, and procedures for manufacturing and testing. Drive cross-functional collaboration ...

Internal Job Description Education / Experience  M.Sc. Analytical/Organic Chemistry/Inorganic Chemistry  Min. 5 years’ Experience in a Quality Control/Analysis laboratory in a cGMP/ISO environment, with exposure to method development and validation activities  Technical skills &  Competencies / Language Technical competence.  Leadership skills.  Analytical ability.  Planning ability.  Communication skills.  Problem solving.  Team building.  KEY ACCOUNTABILITIES  Analysis and approval  Sampling, analysis and ascertaining quality of raw materials, packaging ...

A "QC Manager - Sterile Formulation" job description entails overseeing all quality control operations within a sterile injectable drug manufacturing facility, ensuring that all products meet stringent regulatory standards by managing testing procedures for raw materials, in-process samples, and finished products, while maintaining compliance with cGMP guidelines and conducting thorough ...

Generic Implement Quality Assurance activities for Pharmaceutical at Ankleshwar adhering to standard operating procedures with optimum utilization of resources to ensure consistent good quality of products to meet with customers’ requirements, living Group’s Values and Code of Ethics. Specific additions (if needed)   KEY ACCOUNTABILITIES Quality Management/Continuous Improvement Line Clearance and shop floor compliance Assisting in Complaint ...

Description: Handling BMR- BPR Preparation Filling records as per cGMP RM - PM dispensing Validation Track & Trace Coordination with QA/QC Maintenance Dept, Maintain product quality and process safety Manpower Planning Perform other activities allocated by Production Head    Description: Handling BMR- BPR Preparation Filling records as per cGMP RM - PM dispensing Validation Track & Trace Coordination with QA/QC Maintenance Dept, Maintain product quality and process safety Manpower ...