Quality Control Job Vacancies in Alwar

**We Are Hiring Fabrication Quality Head - Alwar**We are looking for an experienced **Fabrication Quality Head** to lead quality operations at our **heavy fabrication shop in Alwar**. **Key Responsibilities** Lead quality for heavy fabrication operations (laser cutting, bending, welding) Resolve existing welding issues and upgrade welding processes Train welders, track welding parameters, and develop skill matrices Handle **customer audits, third-party inspections, and PDI** Establish strong **in-house quality standards** and ensure smooth handover to clients Supervise the quality team and manage customer communication **Requirements** Welding Engineer (or equivalent qualification) **10-15 years of hands-on experience** in heavy fabrication / construction equipment / similar industries Strong expertise in welding processes and fabrication quality Experience in **customer handling, audits, and team supervision** **Location:** Alwar **Salary:** 35,000 - 60,000 per month (based on experience & skills)If you know someone suitable, feel free to **tag or share** this opportunity.

Role & responsibilitiesQA DocumentationPreparation, review, control, and archival of SOPs, STPs, GTPs, Specifications, and Protocols.Ensure compliance of documentation with cGMP, GLP, and regulatory requirements.Handling of document control system including issuance, reconciliation, and retrieval.Support audit readiness by maintaining updated quality documents.Review of analytical reports, logbooks, and batch-related records.QA Validation & QualificationExecution of Equipment Qualification (IQ/OQ/PQ) for analytical instruments.Preparation and review of validation protocols and reports for process and analytical methods.Cleaning validation and utility qualification support.Preparation of Validation Master Plan (VMP).Coordination with QC and Engineering teams for validation activities as per regulatory guidelines.Quality Management System (QMS)Handling of deviations, CAPA, Change Control, OOS, and OOT investigations.Conduct internal audits and ensure compliance with QMS requirements.Risk assessment and root cause analysis for quality incidents.Monitoring and trending of quality metrics.Preparation and review of quality reports and audit documentation.IPQA (In-Process Quality Assurance)Line clearance and in-process checks during analytical and lab activities.Monitoring of sample handling, testing procedures, and documentation practices.Verification of compliance to SOPs and regulatory guidelines during operations.Review of batch records and analytical test data.Ensuring adherence to Good Laboratory Practices (GLP).QC InstrumentationOperation, calibration, and maintenance of analytical instruments such as HPLC, GC, UV, FTIR, etc.Execution of analytical method validation and instrument qualification.Preparation of calibration and maintenance records.Troubleshooting of instruments and ensuring uptime.Compliance with data integrity and regulatory standards.QC MicrobiologyEnvironmental monitoring and microbial testing.Sterility testing, MLT, BET, and water analysis.Media preparation and growth promotion testing.Handling of microbial cultures and documentation.Ensuring GLP compliance in microbiology laboratory operations.Preferred candidate profileBachelors / Masters Degree in Pharmacy, Microbiology, Biotechnology, Chemistry28 years of experience in QA/QC within a Pharma industrySound knowledge of cGMP, GLP, Data Integrity, and regulatory requirements.