528 Jobs in Boisar - Page 15

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 mai...

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 investiga...

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...

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 pro...

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 ...

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 assess...

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 aligne...

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 Me...

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...

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 s...

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 leve...

Role & responsibilities 1. Quality Control Operations Supervise and perform analysis of in-process and finished pharmaceutical products as per pharmacopeial methods (IP, BP, USP, EP). Ensure timely sampling and testing of batches during manufacturing and post-production. Monitor compliance with Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP) . Conduct HPLC, GC, UV, IR, KF, Dissolution, and other instrumental testing . Maintain and calibrate laboratory equipment. 2. Documentation & Review Review and approve analytical reports, CoAs, and logbooks. Ensure proper documentation of results in LIMS or paper-based systems as per ALCOA+ principles. Investigate OOS, OOT...

Roles and Responsibilities Conduct quality control analysis using GC, HPLC, and other analytical methods to ensure compliance with regulatory requirements. Develop and maintain calibration protocols for laboratory instruments to ensure accuracy and precision of test results. Collaborate with cross-functional teams to resolve issues related to product quality and process optimization. Ensure adherence to cGMP guidelines and regulations in the pharmaceutical industry. Perform routine maintenance tasks on laboratory equipment to prevent downtime and ensure optimal performance. Desired Candidate Profile 2-4 years of experience in a similar role within the pharmaceutical or life sciences industry...

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 which is into Stainless Steel Manufacturing for the below mentioned role. Job Title: DGM/ AGM/ Senior Manager- Learning & Development Location: Boisar Job Description: We are seeking the Learning & Development (L&D) initiatives at steel plant who will play a pivotal role in driving the learning agenda and enhancing employee skills through training programs. Key Responsibilities: Develop and implement a robust learning and development strategy aligned with the steel p...

Inventory Management,Receiving and Storage,Order Fulfillment,Record Keeping,Compliance,Stock Reconciliation,Reporting,SAP EXPERIENCE 2-4 YEARS OFFICE TIMING 7 AM TO 5 PM WEEKLY OFF SUNDAY SALARY 25000 TO 30000 PER MONTH Required Candidate profile QUALIFICATION Graduate,Bcom, MECHANICAL/DIPLOMA OTHER BENEFIT PF,BONUS,LEAVE,MEDICLAIM & ACCIDENTAL POLICY LOCATION RISHIKESH,UTTARAKHAND EMAIL - SURESH@OCEANICHR.COM TEL NO 9820882640

Inventory Management,Receiving and Storage,Order Fulfillment,Record Keeping,Compliance,Stock Reconciliation,Reporting,SAP EXPERIENCE 2-4 YEARS OFFICE TIMING 7 AM TO 5 PM WEEKLY OFF SUNDAY SALARY 25000 TO 30000 PER MONTH Required Candidate profile QUALIFICATION Graduate,Bcom, MECHANICAL/DIPLOMA OTHER BENEFIT PF,BONUS,LEAVE,MEDICLAIM & ACCIDENTAL POLICY LOCATION RISHIKESH,UTTARAKHAND EMAIL - SURESH@OCEANICHR.COM TEL NO 9820882640

Role & responsibilities Oversee end-to-end plant operations including production, QA/QC, engineering, SCM, EHS, and compliance. Ensure adherence to quality standards Manage regulatory inspections and ensure timely closure of observations. Ensure EHS compliance and promote a culture of safety and sustainability. In-depth knowledge of production processes in formulations oral solid dosage, liquids, injectables, etc Preferred candidate profile Ideal Candidate must carry 15+ years of relevant experience into managing overall Plant OR Site Operations. Must have knowledge of formulation. Salary Offered: Best in the industry Interested candidates may share their resumes to tejashree@upman.in OR Cal...

Role & responsibilities oversees and optimizes manufacturing processes, implementing efficient systems, and managing engineering projects . Responsible for leading and mentoring a team of industrial engineers, analyzing production processes, developing strategies for improvement, and ensuring compliance with standards. Key responsibilities include Lean Manufacturing, Six Sigma, cost analysis, and project management. Preferred candidate profile Denim Garment Manufacturing industry experience required

Role & responsibilities Oversees all aspects of facility and equipment maintenance, ensuring smooth operations and a safe working environment . This includes supervising the maintenance team, managing budgets, planning repairs, and maintaining inventory. Key role in implementing safety policies, training staff, and collaborating with external vendors. Preferred candidate profile

Role & responsibilities Handling multiple buyer enquiries from order receipt to payment receipt. Creating production files (Style Sheets, Tech Packs, Spec Sheets, Measurement charts, Patterns, Standard samples, Artworks, Raw Material (RM) BOM, RM & Trim cards, Comment sheets etc.). Pre, post and inline approvals of RM, trims, and production samples. Production coordination with departments. Monitoring production planning and execution to achieve timely deliveries. Updating buyer/management on delivery status. Making & reporting MIS data. Travel for meetings to buyer or supplier offices locally or out station (National). Preferred candidate profile Denim Garment Manufacturing industry experie...

Role & responsibilities optimizing production processes to improve efficiency, reduce costs, and enhance product quality . Analyze workflows, design production layouts, manage production planning and control systems, and ensure efficient resource utilization. Work involves applying techniques like work measurement and motion study, and implementing lean manufacturing principles. Preferred candidate profile Denim Garment Industry experience required

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 which is into Stainless Steel Manufacturing for the below mentioned role. Position Name: Manager / Sr. Manager - HR (Seamless Pipe, SRM Mill, Fastner & Bright Bar) Location: Boisar, Maharashtra Job Purpose: To lead and manage the Human Resources, Industrial Relations, Statutory Compliances, and General Administration functions at the plant level, ensuring alignment with organizational objectives and statutory requirements . Key Responsibilities (KRA): 1. Human Resour...