556 Job openings found

A "FACT Chemist" (often referring to a Formulation, Analytical, Compliance, and Technology Chemist or simply a specialized Manufacturing Chemist) in a personal care products company is responsible for developing, testing, and ensuring the quality of cosmetic products such as lotions, shampoos, and skincare items. They bridge the gap between R&D and mass production, ensuring products are ...

Position:       EHS Manager Location:      Vapi Experience:  10 - 12 Years Industries:   Pharma - API Responsibilities: Ensure compliance with EHS regulations, Factory Act, GPCB, and Pollution Control Board requirements. Manage statutory approvals, hazardous waste disposal, and EHS documentation. Conduct risk assessments (HAZOP/HIRA), incident investigations, and implement CAPA. Handle GMP, regulatory, safety, and customer audits and ensure ...

Designation: QA/QCExperience: 0-2 yearsLocation:Palghar Department: QA & QC Role Summary: The QA & QC – Junior will handle daily IQC, PQC & OQC Of Material and FG Products. Also Manage Quality Related Documents.Key Responsibilities:•Perform incoming inspection of raw materials•Conduct in-process inspections during manufacturing•Perform final inspection of finished Product•Use measuring instruments (vernier caliper, ...

Description: Position:         Sr. Manager - Manufacture & Operation Location:        Ahmedabad Experience:    15 - 20 Years Industries:     Pharma   Responsibilities:         Develop and implement corporate manufacturing strategies aligned with business goals. Monitor production performance across multiple manufacturing sites. Support plant leadership teams to achieve productivity and efficiency targets. Drive continuous improvement ...

Urgent Opening  -Chemist / Officer Experience - 1 Year to 5 years of experiencelocation - Kodadara Jolwa , suratRotational Shift Time - 6am to 2pm2pm to 10pm10pm to 6amGeneral shift - 9am to 6pmCanteen facilityDepartment - Production Department    Operate and monitor production equipment under supervision Follow GMP/GLP guidelines and other industry regulations ...

IPQA activities, Plant round, Online BMR review, Line clearance, Samplingof APIs, Analytical data review, Batch release, APQR preparation. People who have faced regulatory audits like EDQM would be givenpreference.  Process & cleaning validation, including cleaning matrix preparation QMS documentation management; SOP preparation, review, and training IPQA activities to ensure GMP compliance during manufacturing. Regulatory inspection exposure ...

Project Manager – Pharma ProjectsAn Electrical or Mechanical Project Manager in the pharmaceutical industry manages theplanning, design, and implementation of formulation projects (OSD/Injectable) for newmanufacturing facilities, upgrades, or existing plants, ensuring compliance with strictindustry standards and regulations. Key responsibilities include design, contractorsupervision, cost management, and troubleshooting to support production processes, withsignificant overlap ...

  Job Title: Production Officer Location: Sayakha GIDC, Dahej, BharuchIndustry: Chemical ManufacturingExperience Required: 3 to 6 YearsQualification: M.Sc. Chemistry / M.E. Chemical EngineeringSalary (CTC): Will be disclosed at the time of interview Job Summary We are seeking a qualified and experienced Production Officer to oversee and manage production operations in a chemical manufacturing unit. ...

Key Responsibilities Assist in implementation and monitoring of GMP, SOPs, and quality systems Support preparation, review, and control of QA documentation Assist in batch record review and compliance checks Participate in internal audits and inspection readiness activities Support handling of deviations, change controls, and CAPA Assist in raw material, in-process, and finished goods release documentation Coordinate with ...

Key Responsibilities Assist in implementation and monitoring of GMP, SOPs, and quality systems Support preparation, review, and control of QA documentation Assist in batch record review and compliance checks Participate in internal audits and inspection readiness activities Support handling of deviations, change controls, and CAPA Assist in raw material, in-process, and finished goods release documentation Coordinate with ...