249 Jobs in Boisar - Page 5

Responsibilities: * Collaborate with cross-functional teams on MEP projects * Design, test & maintain mechanical systems * Ensure compliance with safety standards * Optimize system performance through mechatronics integration Annual bonus

Role & responsibilities a. Recruitment and Induction b. Performance management c. Training and development d. Employee satisfaction e. Salary , benefits and administration f. Records and statutory g. Disciplinary process h. Grievance management i. Employee Engagement 1. Dept Organogram Update Preferred candidate profile 4. Profile: Exposure to all aspects of Recruitment, Life Cycle, Payroll, Induction, Compensation, Performance, Incentives, Training, Increments, Gradation, Attrition, IR, Liaison, Statutory Compliances and Legal Procedures. Must have full exposure to industrial statutory compliances. Preferred Candidate : Male preference

Execute preventive, predictive, and breakdown maintenance of production and utility equipment (e.g., HVAC, AHU, air compressors, chillers, boilers, WFI/RO systems, etc.). Troubleshoot mechanical, electrical, and instrumentation issues to minimize downtime. Prepare and maintain SOPs, maintenance logs, calibration records, and equipment qualification documents (IQ, OQ, PQ). Ensure compliance with cGMP, GDP, and safety standards. Participate in internal and external audits (e.g., USFDA, MHRA, WHO, etc.). Support installation and commissioning of new equipment and utilities. Assist in engineering change controls, validations, and equipment upgradation. Monitor energy consumption and suggest improvements for utility efficiency. Implement engineering best practices to reduce downtime and maintenance costs

Job Title: QC Executive Job Location: Boisar Years of Experience: 1-5years Salary: 1lacs-3lacs Working Days: Monday to Saturday Key Responsibilities: 1. Quality Inspection & Testing: Conduct inward inspection of raw materials to ensure they meet quality specifications. Perform in-process inspections to identify and resolve quality issues during production. Carry out pre-dispatch inspections to ensure final products meet customer and regulatory standards. Conduct online inspections to monitor and improve product consistency. 2. Testing Equipment & Analysis: Operate and maintain UTM (Universal Testing Machine) for mechanical property testing. Perform MFI (Melt Flow Index) testing to assess polymer flow characteristics. Use Viscometer to evaluate viscosity and flow behavior of materials. Record and analyze test results, preparing detailed quality reports. 3. Compliance & Documentation: Ensure compliance with industry quality standards and company policies. Maintain proper documentation of inspections, test results, and deviations. Report any non-conformities and assist in root cause analysis and corrective actions. 4. Process Improvement: Work closely with the production team to improve processes and minimize defects. Suggest and implement corrective and preventive actions for quality issues. Participate in audits and support continuous improvement initiatives. Key Skills & Competencies: Technical expertise in handling UTM, MFI, Viscometer, and other quality control instruments. Strong understanding of quality control processes, raw material testing, and finished goods inspection. Ability to analyze test results and implement corrective actions. Knowledge of ISO standards and quality assurance procedures. Strong attention to detail and problem-solving abilities. Proficiency in MS Office (Excel, Word) and ERP systems.

Plan and execute preventive maintenance schedules for critical equipment (HVAC, AHUs, boilers, chillers, WFI, RO systems, autoclaves, etc.). Troubleshoot and resolve breakdowns in coordination with cross-functional teams. Support IQ/OQ/PQ of new and existing equipment. Ensure timely calibration of instruments as per the calibration schedule. Monitor and manage the operation of utilities such as purified water systems, HVAC systems, compressed air, and electrical systems. Maintain utility logbooks and ensure adherence to SOPs and GMP norms. Maintain engineering documents like machine history cards, maintenance logs, and calibration records. Ensure compliance with cGMP, FDA, WHO, and other regulatory guidelines. Assist in new equipment installation and facility modifications. Coordinate with vendors and contractors for engineering projects.

Operate and monitor packing machinery for dry powder pharmaceuticals. Ensure that powder is packed in correct quantities, weights, and packaging specifications. Perform routine checks to maintain machinery in optimal working condition. Verify packaging materials, labels, and batch records to ensure compliance with regulatory and quality standards. Perform in-process inspections and checks to ensure proper filling, sealing, and labeling. Report any deviations or discrepancies to the supervisor and take corrective actions. Follow all GMP guidelines and maintain a clean and safe working environment. Ensure compliance with SOPs (Standard Operating Procedures) and regulatory requirements. Maintain proper documentation for all packing activities and related records. Work closely with production, quality control, and warehouse teams to ensure timely production schedules are met. Assist with training new staff on packing procedures and equipment. Participate in ongoing training to improve packing processes and stay current with industry best practices. Identify opportunities for process optimization and work with management to implement improvements.

Oversee the daily operations of the packaging department, ensuring the timely and efficient packing of pharmaceutical products. Supervise and guide the packing team to ensure adherence to production schedules. Ensure the packing area is organized, clean, and compliant with GMP (Good Manufacturing Practice) guidelines. Coordinate with other departments like Quality Control, Supply Chain, and Production to align on daily targets and deliveries. Ensure that the packaging process adheres to all GMP, GLP (Good Laboratory Practice), and regulatory requirements (FDA, WHO, etc.). Monitor and ensure that proper documentation is maintained for each batch (batch records, labeling, and packaging). Conduct in-process checks to ensure that the packing is done in accordance with the standard operating procedures (SOPs). Oversee the operation and maintenance of packing equipment and machinery. Ensure that packing machines are calibrated and maintained properly. Coordinate with maintenance staff for the timely servicing and repair of equipment. Monitor and maintain the efficiency of packing lines and troubleshoot any issues that may arise during production. Identify areas of improvement in the packing process to enhance productivity. Assist in implementing continuous improvement projects to optimize packing operations. Maintain adequate inventory levels of packing materials (bottles, cartons, labels, etc.). Work with the supply chain department to ensure smooth availability of materials and resolve any shortages or delays.

Role & responsibilities In-Process Checks. Process Validation Support. Documentation & GMP Compliance. Training & Audit Readiness Continuous Improvement Preferred candidate profile More than 10 years of experience in OSD Formulation is preferred. Should be B.Pharm & M.pharm qualified. Immediate joiner or max 30 days joining is preferred

Responsibilities: * Ensure optimal plant performance through preventative & breakdown maintenance * Collaborate with cross-functional teams on capital projects * Manage utility systems & machinery maintenance Annual bonus

Location: Boisar Experience: Fresher - 2 yrs Job Responsibilities: * Conducting plant trials at the manufacturing site as needed. * Performing material characterization using Differential Scanning Calorimetry (DSC) and Thermogravimetric Analysis (TGA). * Working with Smart Polymers and Polymer Synthesis processes. * Handling Extrusion Molding operations. * Supporting R&D initiatives to enhance material properties and product performance. * Collaborating with cross-functional teams to optimize formulations and manufacturing processes. Desired Candidate Profile: * Educational Background: B tech / M tech in Polymers, Material Science, Technical Skills: * Strong knowledge of DSC, TGA, Smart Polymers, Polymer Synthesis, and Extrusion Molding. * Hands-on experience with polymer material testing and processing techniques. Other Requirements: * Ability to conduct trials and research at plant locations. * Strong problem-solving and analytical skills. * Good communication and teamwork skills. If you are interested, please share your updated resume with us at recruitment@illusiondental.com or WhatsApp 8657025718.

Role & responsibilities Office Administration: Oversee day-to-day administrative tasks in the factory/office. Maintain office supplies, equipment, and facility infrastructure. Manage housekeeping, security, and pantry services. Documentation & Records: Maintain proper filing and documentation for administrative and operational records. Assist in preparing reports, presentations, and correspondence. Ensure all statutory records and licenses are updated and compliant. Vendor Management: Coordinate with external vendors and service providers. Process purchase orders and verify vendor invoices. Track and manage vendor contracts and renewals. HR & Payroll Support (as needed): Assist HR with attendance records, leave management, and onboarding documentation. Support coordination for training, audits, and employee engagement events. Compliance & Safety: Ensure adherence to facility safety standards and regulatory compliance. Maintain visitor and gate pass records. Coordinate with government bodies and local authorities when required. Travel & Logistics: Arrange travel, accommodation, and transportation for staff and visitors. Manage courier and logistics-related activities. Qualifications & Skills: Bachelor's degree in Business Administration or relevant field. 4+ years of experience in administrative roles, preferably in a manufacturing/industrial setting. Proficiency in MS Office (Word, Excel, PowerPoint). Good communication and interpersonal skills. Strong organizational and time management abilities.

Role & responsibilities Manage cost control initiatives, analyze invoices, reduce leakages Handle GRN, vouchers, petty cash, inward/outward registers Oversee attendance records and coordinate payroll inputs Liaison with government bodies and external agencies Ensure smooth functioning of front desk, security, housekeeping, pantry, stationery supply Manage admin budget planning and vendor payments Maintain communication services (mobile connections, billing) Preferred candidate profile 3-8 years in factory / plant administration, facility management, office admin Local candidates from Boisar, Palghar, Tarapur MIDC, Vasai preferred

Supervise day-to-day operations of the external preparation manufacturing section. Ensure proper execution of batch manufacturing processes as per Batch Manufacturing Records (BMRs) and Standard Operating Procedures (SOPs). Coordinate with Quality Assurance (QA), Quality Control (QC), Warehouse, and Maintenance for smooth operations. Monitor equipment calibration, cleaning, and maintenance to ensure readiness for production. Ensure proper line clearance, area cleaning, and equipment readiness before starting manufacturing operations. Review and maintain manufacturing documentation, including BMRs, logbooks, and deviation reports. Handle in-process checks and ensure process parameters are maintained within specified limits. Train and guide operators and junior staff in GMP practices and SOP adherence. Investigate deviations and support in root cause analysis and implementation of CAPA. Ensure compliance with EHS (Environment, Health, and Safety) standards within the manufacturing area.

Supervise day-to-day operations of Dry Powder Filling, Mixing, and Packing activities. Ensure batch manufacturing records (BMR) and other documentation are filled accurately and in a timely manner. Ensure cleanroom discipline and maintain the required environmental conditions in the production area. Coordinate with QA, QC, Maintenance, and Warehouse departments for uninterrupted production. Follow and enforce adherence to Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP). Perform and supervise line clearance, cleaning, and sterilization procedures for equipment and areas. Maintain production logs, equipment usage logs, and cleaning records . Participate in investigations (deviations, incidents, and OOS) and implement corrective/preventive actions. Train new operators and assistants in processes and GMP standards. Monitor and report on yield, wastage, and productivity metrics. Ensure compliance with regulatory and safety requirements (USFDA, MHRA, WHO, EHS, etc.).

Manpower Resources India Pvt. Ltd is a leading Executive Search & Selection company, caters to recruitment services in Manufacturing, Infrastructure, Engineering & Healthcare domain. We have been mandated by a large conglomerate into Stainless Steel Manufacture. Job Title : Engineer / Sr. Engineer / Assistant Manager / Deputy Manager EHS Department : SRM / Bright Bar / Fastener / Pipe Plant Location : Boisar, Maharashtra Experience : Minimum 3 + Years Qualification : BE / B.Tech in Mechanical, Production, or Metallurgy OR B.Sc. / Diploma in Mechanical Engineering Mandatory: Diploma in Industrial Safety from a recognized institute Role & Responsibility Safety Officer - EHS audit trackers sent to respective Bay owners & Monthly EHS review report/PPT). - Monthly EHS monitoring & Audits of all respective area is done and reports submitted to all concerned HODs/Bay Owners for necessary action/compliances. - Co-ordination with Bay Owners/HODS for necessary compliances against raised EHS related Issues/Observation/Non-Conformances in his respective units/area. - Co-ordination with out-sourced agency during Periodical Environmental Monitoring in the respective units - Preparation of Monthly EHS review report/PPT for CMD Sir/TOP Management, under guidance of Head (EHS) - Calculation of OT hours and cost & provide input to functional head for necessary action. - Monitoring of EHS statutory requirements & their status of Compliances and report to HOD (EHS) for further action/coordination with MPCB/DISH. - Monitoring the Work Permit System for elimination of Unsafe work condition & Unsafe work acts. - Scheduled EHS training (Induction of new joiners, EHS training & Awareness to existing workmen, Tool Box training etc. on various topics & covering the all respective workmen - Organize the EHS related event Celebration like National Safety Day, World Environment Day etc. - Conducting the Weekly EHS Committee Meeting for review the EHS related issues and their action plan/taken - Quarterly Mock drill for prevention of fire & handling of emergency situation - Periodical Monitoring & maintenance of Fire Extinguishers placed in various sections of all respective units. - For implementation of ISO 14001 & OHSMS 45001 certification & Coordination with consultants & Bay owners - Coordination with competent agency during their visit at plant site for inspection of Lifting Tools & Tackles, Safety Audits and related tasks. - Prepare the List of Contents of First Aid Box. Decide the location of its availability point. Weekly check and replenish the items below the minimum level or expired. - In case of accidents occur, attend the accident place and provide necessary first aid. If requires take the injured person to OHC/Hospital for further treatment. Records such accidents in Accident register. - Investigate the root cause and take appropriate corrective action to avoid reoccurrences and maintain

Operate and monitor compression machines (e.g., Cadmach - ACC). Ensure smooth execution of batch production as per BMR/BPR and SOPs. Carry out in-process checks (IPC) like weight variation, hardness, thickness, friability, etc. Perform machine changeovers, cleaning, and line clearance. Maintain and update Batch Manufacturing Records (BMRs), logbooks, equipment usage logs. Adhere strictly to cGMP, GDP, and safety norms. Participate in audits (internal/external) and handle compliance requirements. Collaborate with QA, maintenance, and validation teams. Report deviations, breakdowns, and implement corrective/preventive actions (CAPA). Suggest and implement process improvements for yield and productivity.

Execute daily coating production activities as per batch production records (BPRs). Supervise the mixing, blending, and application processes for various coating formulations. Ensure proper setup and maintenance of coating equipment (e.g., mixers, spray booths, curing ovens). Monitor in-process parameters and adjust formulations or processes to maintain product quality. Ensure compliance with ISO, GMP, and EHS guidelines. Coordinate with QC and R&D teams for sampling, trials, and product validation Maintain accurate production records, logs, and shift reports. Assist in preparing Standard Operating Procedures (SOPs) and work instructions. Report deviations, rejections, and ensure corrective actions are taken. Monitor raw material usage, stock levels, and report shortages. Ensure timely requisition and transfer of materials from the store to production.

Monitor day-to-day operations to ensure adherence to GMP guidelines. Conduct routine inspections and walkthroughs on the shop floor. Identify non-compliance areas and coordinate corrective/preventive actions (CAPA). Review and update Standard Operating Procedures (SOPs), batch records, and other GMP-related documentation. Ensure proper documentation practices (GDP) are followed across departments. Assist in internal audits and regulatory inspections (e.g., FDA, MHRA, WHO, TGA). Coordinate audit responses and track closure of observations. Organize and conduct GMP training for staff at all levels. Promote a quality culture through awareness programs and initiatives. Participate in risk assessments and deviation investigations. Ensure timely reporting and escalation of critical quality issues. Recommend and implement process improvements related to GMP compliance. Support cross-functional teams in quality initiatives and validation activities.

Review and approve validation protocols (IQ/OQ/PQ), reports, and related documentation for manufacturing equipment, utilities, and processes. Provide QA oversight during the planning and execution of process validation and cleaning validation activities. Ensure all validation activities are conducted in accordance with current Good Manufacturing Practices (cGMPs), company policies, and industry standards. Participate in risk assessments (e.g., FMEA) to support validation strategy development. Support investigations and change controls related to validated systems or processes. Collaborate with Manufacturing, Engineering, QC, and Regulatory Affairs to ensure validation deliverables are aligned with product quality requirements. Maintain validation documentation and ensure data integrity in all QA records. Conduct QA review and approval of protocols and reports for re-validation and periodic reviews. Support internal and external audits and inspections, providing SME support for validation topics.

Maintain control of documents such as SOPs, work instructions, forms, policies, and records. Ensure documents are reviewed, approved, updated, and archived per document control procedures. Maintain the Document Control Register and Master List of Documents. Assist in the preparation of quality manuals, procedures, and other QMS documentation. Support the implementation and maintenance of ISO 9001 (or other applicable QMS standards). Assist in internal audits, including audit preparation, scheduling, and tracking corrective/preventive actions (CAPA). Monitor and report QMS performance through KPIs, nonconformance records, and continuous improvement initiatives. Coordinate Management Review Meetings and maintain related documentation. Ensure adherence to regulatory, statutory, and customer-specific quality requirements. Participate in external audits (e.g., certification audits, customer audits). Help prepare documentation for regulatory submissions or inspections as required. Maintain records related to quality objectives, customer complaints, NCRs, and audit findings. Generate reports on QMS performance, deviations, and document revisions. Ensure traceability and version control of all critical documents.

Monitor compliance with GLP, GMP or other applicable standards. Maintain and update SOPs (Standard Operating Procedures). Review laboratory notebooks, worksheets, and analytical reports. Assist in internal and external audits. Ensure accurate documentation of QA activities and laboratory testing. Review COAs (Certificates of Analysis) and batch records. Manage deviation reports, CAPAs, and change control processes. Assist in the qualification/validation of equipment, methods, and software. Ensure timely calibration and maintenance of lab instruments.

Monitor all in-process manufacturing and packaging activities on the shop floor. Perform line clearance before manufacturing/packaging starts. Verify batch records and ensure adherence to SOPs and BMR/BPR entries. Check critical control points and parameters during manufacturing. Review batch manufacturing records (BMR), batch packaging records (BPR), and logbooks in real time. Ensure timely and accurate documentation of in-process observations. Escalate any deviation or non-conformance observed during the process. Ensure compliance with cGMP, GDP, and regulatory requirements. Assist in handling deviations, change controls, and CAPAs. Participate in internal audits and regulatory inspections. Verify the status and calibration of equipment before use. Ensure proper labeling, handling, and storage of materials.

Oversee line clearance , in-process sampling, and real-time review of batch manufacturing & packaging records (BMR/BPR) Monitor critical process parameters (e.g., weight variation, leak tests), hygiene, documentation, calibration, and equipment qualification Lead investigations for deviations, OOS/OOT results, non-conformities; drive CAPA and root cause analysis Approve/reject batches, handle change-controls and disposals, and manage legal/retention samples Support and participate in internal, external, and regulatory audits/inspections ; ensure audit readiness Prepare, review, and maintain SOPs, protocols (validation, cleaning, process), quality documentation, and MIS reporting

Supervise and coordinate QA lab personnel and activities related to sampling, testing, and reporting of raw materials, in-process samples, and finished products. Ensure compliance with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and regulatory guidelines (e.g., FDA, ISO, ICH, etc.). Review and approve analytical test results, COAs (Certificates of Analysis), and related documentation. Manage calibration, maintenance, and validation of laboratory instruments (e.g., HPLC, GC, UV-Vis, FTIR). Investigate out-of-specification (OOS), out-of-trend (OOT), and non-conformances; participate in root cause analysis and CAPA implementation. Ensure timely completion of stability studies and trending of data.

Role & responsibilities Production Planning & Scheduling: Develop and implement production plans to meet project timelines and customer requirements. Coordinate with project management and other departments to ensure seamless execution. Team Management: Lead, mentor, and manage a team of supervisors, operators, and technicians. Ensure high productivity and adherence to quality standards. Quality Control: Establish and monitor quality control processes in collaboration with the QA team to deliver defect-free products. Process Optimization: Continuously improve manufacturing processes to enhance efficiency, reduce costs, and integrate best practices. Inventory Management: Manage inventory levels of raw materials and components. Coordinate with procurement for timely material availability. Health & Safety Compliance: Ensure compliance with all safety and regulatory standards. Promote a strong safety culture across the production floor. Cross-functional Collaboration: Work closely with engineering, design, and sales teams to address technical requirements and production feasibility. Continuous Improvement: Analyze KPIs, identify improvement areas, and drive initiatives for operational excellence. Preferred candidate profile Hands-on experience in Production / Manufacturing / Planning in heavy fabrication, process equipment manufacturing, or capital goods industry Strong background in managing fabrication of pressure vessels, heat exchangers, reactors, dryers, condensers, columns, storage tanks, skid systems Experience working in ASME / IBR / ISO 9001 certified fabrication shops Prior exposure to welding, machining, quality control, shop floor management