Technical Operator

Position: Technical Operator - Assembly Quality and ProductionJob Location: Kotputli, Jaipur, Rajasthan (India)Work Duration: 8 hours/dayGender Requirement: Male OnlyJob Role: Responsible for operating, monitoring, and maintaining production machinery in the pharmaceutical unit. Involves work in assembly, quality control, and production processes to ensure smooth manufacturing operations as per industry standards.Stipend/Salary:ITI: ₹12,720/- (₹11,220 + ₹1,500)Diploma: ₹16,000/-Graduation: ₹15,050/-Additional benefits: Free canteen, transport, dress & shoes.Accommodation:First week free at the company guest house.Afterward, paid by candidate (shared room ₹1,000–1,200/month).Required Documents:All qualification certificatesAadhaar Card & PAN CardResume with email ID5 passport-size photosBank passbook/cancelled chequeKey Responsibilities 1. Machine Operation and Monitoring Operate pharmaceutical machinery such as capsule fillers, tablet press machines, blenders, granulators, blister packing machines, and coating systems, depending on the production line. Ensure proper machine start-up, calibration, and shut-down procedures are followed as per batch manufacturing records (BMR). Monitor production processes, machine speed, temperature, humidity, and pressure to ensure optimal performance. Detect any mechanical issues or irregularities in real-time and escalate to the maintenance or engineering team as needed. 2. Assembly Processes Perform manual or semi-automated assembly tasks including packing, labeling, and container sealing for tablets, capsules, syrups, or injectable products. Maintain hygiene and aseptic techniques during the assembly and handling of pharmaceutical products. Ensure correct usage and handling of primary and secondary packaging materials as per specifications. 3. Quality Control and Compliance Conduct in-process quality checks (IPC) including weight variation, hardness testing, visual inspection, and sealing integrity, as required by the batch protocol. Report and document any deviations, non-conformities, or quality concerns immediately to the Quality Assurance (QA) team. Record data accurately in logs, BMRs, and other documentation forms to ensure traceability and audit readiness. 4. Documentation and Record-Keeping Maintain production records, equipment usage logs, cleaning records, and batch processing documents with accuracy and in a timely manner. Follow GDP (Good Documentation Practices) to ensure data integrity and regulatory compliance. Support preparation for audits by maintaining clean, organized, and fully documented production areas. 5. Cleaning and Sanitization Perform cleaning and sanitization of equipment, production areas, and machinery according to cleaning SOPs. Conduct line clearance and area readiness checks before and after each production batch. Ensure compliance with cross-contamination prevention protocols and cleanroom procedures. 6. Safety and Environmental Control Follow all EHS (Environment, Health & Safety) protocols strictly, including wearing prescribed Personal Protective Equipment (PPE). Identify and report potential safety hazards and actively participate in safety drills and training. Handle pharmaceutical ingredients and hazardous materials with care and proper precaution. 7. Coordination and Communication Collaborate with QA, Maintenance, Warehouse, and Planning teams to ensure uninterrupted production. Communicate issues promptly to supervisors or team leaders for timely resolution. Participate in shift handovers and daily briefings to stay aligned with production targets and updates. 8. Continuous Improvement Suggest ideas to improve operational efficiency, reduce waste, and enhance product quality. Participate in root cause analysis (RCA), corrective and preventive action (CAPA) meetings, and lean manufacturing initiatives. Engage in cross-training to support multiple machines or production lines.Skills and Competencies Technical Knowledge: Familiarity with pharmaceutical machinery and production environments. GMP and Compliance Awareness: Understanding of Good Manufacturing Practices and industry regulations (e.g., WHO, USFDA, MHRA). Attention to Detail: Strong focus on quality, precision, and cleanliness. Problem-Solving: Ability to identify and resolve operational or equipment issues. Documentation: Ability to maintain accurate and compliant records. Teamwork: Collaborative approach in working with cross-functional teams. Basic Computer Skills: Proficiency in entering data in logbooks or electronic systems (if applicable). More information about this Technical Operator - Assembly Quality and Production JobPlease go through the below FAQs to get all answers related to the given Technical Operator - Assembly Quality and Production jobWhat are the job requirements to apply for this Technical Operator - Assembly Quality and Production job position? Ans: A candidate must have a minimum of fresher as an Technical Operator - Assembly Quality and Production What is the qualification for this job? Ans: The candidate can be a Graduate from any of the following: BSc What is the hiring Process of this job? Ans: The hiring process all depends on the company. Normally for an entry level, hiring the candidate has to go for Aptitude, GD (If they look for communication),Technical test and face to face interviews.This Technical Operator - Assembly Quality and Production is a work from home job? Ans: No ,its not a Work from Home Job. How many job vacancies are opening for the Technical Operator - Assembly Quality and Production position? Ans: There are immediate 1 job openings for Technical Operator - Assembly Quality and Production in our Organisation.

BSc(Chemistry / Applied Chemistry)

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