359 Quality Documentation Jobs - Page 4

We are seeking a knowledgeable and detail-oriented IRIS Audit Specialist to oversee and execute Quality Management System (QMS) audits in alignment with the International Railway Industry Standard (IRIS) , specifically ISO 9001 and ISO 22163 . The ideal candidate will bring a solid understanding of quality principles, railway industry standards, and auditing techniques. They will play a key role in planning, conducting, and reporting IRIS audits and guiding continuous improvement initiatives within the organization. Key Responsibilities: Plan, schedule, and conduct internal IRIS audits in accordance with ISO 22163 and ISO 9001 standards. Use the IRIS Audit Tool and Portal for accurate audit execution and documentation. Evaluate the effectiveness of Quality Management Systems using a process-based, risk-driven approach. Review and assess compliance with railway-specific requirements, including operational and regulatory standards. Identify, document, and classify non-conformities; support the implementation of corrective and preventive actions (CAPA). Deliver clear and concise audit findings and reports to relevant stakeholders. Monitor follow-up actions to ensure timely closure of audit issues and drive continuous improvement. Liaise with external auditors and support third-party IRIS certification or surveillance audits. Train and guide internal teams on IRIS requirements, audit readiness, and QMS best practices. Analyze IRIS performance levels and contribute to achieving higher ratings (e.g., Silver, Gold). Keep updated with industry changes, IRIS portal updates, and evolving regulatory requirements. Required Qualifications & Skills: Bachelor's degree in Engineering, Quality, Industrial Management, or related field. Minimum [X] years of experience in Quality Management or IRIS auditing within the railway or industrial manufacturing sector. Strong knowledge of ISO 9001 and ISO 22163 (IRIS Standard). Proven experience in conducting IRIS audits , including audit planning, execution, and reporting. Proficiency with audit techniques such as interviewing, observation, and document review. Familiarity with the IRIS Audit Tool and IRIS Portal usage. Experience in non-conformance management and CAPA processes . Strong communication, interpersonal, and presentation skills. Ability to work independently and collaboratively across cross-functional teams. Detail-oriented mindset with a commitment to continuous improvement . Preferred Certifications: Certified ISO 9001 Lead Auditor or equivalent. IRIS Auditor Certification (if applicable or preferred). Six Sigma or Lean certification (optional but beneficial).

Responsibilities: * Conduct quality audits using ISO standards * Ensure compliance with PPAP documentation requirements * Maintain accurate computer records for quality management systems Provident fund

Post - QMS -Manager Qualification : BE Electrical or Electronics Location Pune chakan Contact - 9356395439 Email - jobpune12@gmail.com Experience : 5 + yrs experience in control Panel manufacturing Salary : No bar for the right candidate. QMS Development and Implementation: Establishing and maintaining the QMS according to relevant standards like ISO 9001, AS9100, or IEC 61439-1 & 2, as applicable. Compliance: Ensuring adherence to all relevant standards, regulations, and customer requirements. Documentation: Managing and controlling QMS documentation, including procedures, work instructions, and control plans. Audits: Conducting internal audits, coordinating external audits, and managing responses to audit findings. Non-Conformance Management: Identifying, investigating, and resolving non-conformities, implementing corrective and preventative actions (CAPA). Customer Complaints: Managing customer complaints, conducting root cause analysis, and implementing preventive measures.

Job Responsibilities Operations Build successful relationships with Life Sciences (LS) client stakeholders to promote confidence in quality and compliance, as well as forward planning. Provide management and leadership direction for the development and implementation of quality and compliance programs. Collaborate with other Life Sciences accounts to proactively accumulate, share and reapply all learnings, successes as well as best practices. Collaborate with Global Life Sciences Quality Vertical for development, revision and implementation of QMS and quality documents. Responsible for ensuring Lide Sciences facilities teams adhere to the required training and ensuring in compliance to clients QMS and quality training requirements. Responsible for ensuring that the work conducted by the Facilities team, and its subcontractors is in full compliance with contractual requirements, clients SOPs, GxP, FDA and other regulations. Able to perform/support internal JLL compliance audits and prepare SOPs, and training materials for use by the Life Sciences facilities team in the performance of their work. Guide Life Sciences facilities team in closing recommendations from clients audit. Expected to interface with the clients quality personnel to ensure that all of the clients SOPs are followed, work performed by the LS facilities team is properly documented for traceability in the framework of GDP. Sustain quality assurance support and develop a Quality Engineering Maintenance program for a controlled-environment manufacturing and laboratory facility as it relates to the facilities maintenance of this plant. Conduct investigations and drive accountability for all quality events. Lead programs to create value for client to ensure program deliveries meet or exceed expectations. Facilitate quality-relevance investigation via structured Root Cause Analysis. As part of career development, lead Life Sciences accounts as an IFM leader.Reporting Manage and report on critical & key performance measurements. Develop and submit periodic site status reports related to the Quality Program. People Management Effectively lead and guide a Life Sciences Quality team by clearly communicating expectations, accountabilities and providing performance feedback for continuous improvement. Ensure Life Sciences Operations team members complete relevant quality and compliance training. Coach new Life Sciences team members on quality and compliance for their adaptation into specific Life Sciences accounts. Mentor, develop and train peer and direct report team members. Provides direction/information to vendors, facilities staff and service providers as required to ensure that quality assurance expectations are communicated and followed.Others Any other quality-relevant duties and tasks assigned. Knowledge, Skills & Abilities. MINIMUM REQUIRED / PREFERRED - Education/training Bachelor degree preferred Degree in science, technical or relevant discipline Sound fundamental knowledge in process utilities. 6+ Years of relevant experience preferred with minimum 4+ years in Quality and Compliance discipline in GxP manufacturing or laboratory environment. Six-Sigma and Root Cause Analysis training is essential. Skills and knowledge Background in technical documentation Work independently and within a team. Strong mindset of compliance and client-focus. Communicate effectively with technical, quality assurance and other personnel. Proficient in Word, Excel and other Microsoft Office Suite programs Ability to investigate, recognize and diagnose trends and patterns. Solid understanding of cGMPs as they relate to the performance of maintenance and repairs to facilities, utilities and equipment utilized for the manufacturing plants and laboratories for drug products. Experience working at an FDA regulated manufacturing facility in a quality assurance or quality control capacity. Support investigations and corrective action plans for appropriate discrepancies. Investigation of compliance issues as required, collaborating with relevant Compliance Partner(s) Understanding of FDA regulations including 210 CFR part 210 and 211. Strong commitment to quality assurance, and a willingness to help develop a quality first culture on the site. Knowledge of Quality Engineering techniques, CMMS systems, and Quality Management Systems English communication is essential Other abilities Good oral and written communication skills including the ability to communicate to all levels of management and willing to interface with a diverse customer base including technical and non-technical personnel.Physical work requirements and work conditions Familiar with process utilities and GxP environment.

Responsibilities: * Conduct quality inspections & audits * Ensure compliance with quality standards * Manage raw material inspections * Oversee quality control processes * Monitor product quality throughout production cycle

Track and Trace Analyst Job Description Your Job Do you thrive in fast-paced environments where coordination, communication, and precision are keyDo you love solving logistical puzzles to create smooth, on-time deliveries At Kimberly-Clark Professional (KCP), were looking for a Track & Trace Analyst to join our North America Customer Care team. In this role, you ll be the critical connection point between customers, transportation partners, and internal teams ensuring every shipment is tracked, every exception is resolved, and every delivery meets customer expectations. Youll lead initiatives, tackle complex problems, and make real impact on the customer experience. About Us Huggies . Kleenex . Cottonelle . Scott . Kotex . Poise . Depend . Kimberly-Clark Professional . You already know our legendary brands and so does the rest of the world. In fact, millions of people use Kimberly-Clark products every day. We know these amazing Kimberly-Clark products wouldn t exist without talented professionals, like you. At Kimberly-Clark, you ll be part of the best team committed to driving innovation, growth, and impact. We re founded on more than 150 years of market leadership, and we re always looking for new and better ways to perform so there s your open door of opportunity. It s all here for you at Kimberly-Clark. Led by Purpose. Driven by You. About You Youre detail-obsessed and customer-focused. You love tracking down the why behind delays, keeping teams informed, and identifying ways to improve how things move. We d love to meet you if you: Hold a Bachelor s degree and have at least 2 years of related experience OR 5 years of relevant professional experience. Are comfortable working in 5:00 P.M to 2:00 A.M shifts Have strong working knowledge of SAP, TMS, and order management tools. Are fluent in Microsoft Excel and other MS Office tools. Communicate clearly verbally and in writing especially in high-pressure situations. Have leadership qualities and enjoy mentoring peers. Excel at project management and multitasking. Enjoy cross-functional collaboration and influencing others toward results. Have a working knowledge of Lean Six Sigma tools (preferred). Are comfortable working with delivery analytics and reporting systems. Are passionate about delivering a great customer experience and improving the systems that support it. Responsibilities As a Track & Trace Analyst, your role will be a mix of coordination, analysis, problem-solving, and leadership. You will: Manage order shipments through the entire fulfilment cycle using SAP, TMS, and Service Cloud. Provide proactive and transparent communication on delivery status and failures internally and externally. Coordinate rescheduling and appointment confirmations with customers and carriers. Lead delivery exception processes, escalating risks and recommending preventive actions. Drive process improvements using Lean Six Sigma principles to enhance the customer journey and reduce cost-to-serve. Analyse performance metrics and delivery KPIs, providing insights and trends to improve service. Own internal shipment visibility tools such as Four Kites and Control Tower. Collaborate closely with teams across transportation, planning, marketing, sales, order management, and distribution. Handle inquiries routine and complex with professionalism and accuracy. Provide training and mentorship to teammates to raise departmental standards. Support customer escalations with empathy and ownership, driving toward resolution. Maintain high-quality documentation and process compliance. To Be Considered Click the Apply button and complete the online application process. A member of our fabulous recruiting team will review your application and then get in touch with you if you seem like a good fit for this role to begin the official interview process. To prepare for the interview process, you can check out the Careers area on our website . And finally, the fine print For Kimberly-Clark to grow and prosper, we must be an inclusive organization that applies the diverse experiences and passions of its team members to brands that make life better for people all around the world. We actively seek to build a workforce that reflects the experiences of our consumers. When you bring your original thinking to Kimberly-Clark, you fuel the continued success of our enterprise. We are a committed equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, sexual orientation, gender identity, age, pregnancy, genetic information, citizenship status, or any other characteristic protected by law. This role is available for local candidates already authorized to work in the role s country only. Kimberly-Clark will not provide relocation support for this role. Employment is subject to verification of pre-screening tests, which may include drug screening, background check, and DMV check. LI-Hybrid Primary Location India - Pune Additional Locations Worker Type Employee Worker Sub-Type Regular Time Type Full time

Role & responsibilities 1.Issurance of BMR,ECR to production Department. 2. Issuance ofprotocol to QC deparlment & other formats to respective department. 3. Issuance offinished product labels and seal. 4. To maintain, check and retention fi1led BMR, QC reports, formats and other filled records that are received from production, quality control and other departrnents. 5.To issue and Handling of change control,deviation,OOS reports and maintain their records. 6.To co-ordinate durins intemal audit. 7. To take QA round or as per SOP's. 8. To do any other supporting work in absence of any other staff from department as per instructior given by department head. 9. To prepare and review master documents such as BMR, MFR, SOP's and other documents. 10. To prepare and review validation protocol and report. 11. To prepare and review annual product quality review (APQR). 12. To prepare and review RA related documents. 13. Comnliance for audit observation. 14. Risk analysis protocol & report preparation. 15. In absence QA manager Release and dispatch co-ordination along with QA/warehouse and

Job Title: Asst. Manager / Manager Quality Control Department: Quality Control Number of Opening – 1 Nos Experience Required: 5 to 10 Years Location: At Factory – Daheli, Valsad, Gujarat Reports To: Quality Head Job Purpose: To ensure that all raw materials, in-process production, and finished goods meet the required quality standards. The QC Manager is responsible for implementing and maintaining quality systems, reducing rejections, and ensuring customer satisfaction through consistent product quality. Key Responsibilities: 1. Quality System Implementation: Develop, implement, and maintain quality control procedures and inspection plans. Establish and monitor quality parameters (bursting strength, GSM, moisture, compression, dimensions, etc.). Ensure compliance with internal standards and customer specifications. 2. Incoming Material Inspection: Inspect incoming raw materials (kraft paper, adhesives, inks, etc.) as per quality norms. Approve or reject materials based on test reports. Coordinate with purchase and stores for rejected material replacement. 3. In-Process Quality Control: Monitor and control quality during various stages of production (corrugation, printing, slotting, die-cutting, pasting). Ensure process control measures are followed by operators and supervisors. Conduct root cause analysis and implement corrective/preventive actions for defects. 4. Finished Goods Inspection: Conduct final inspection of finished goods before dispatch. Ensure packing, labeling, and quantity checks as per customer requirement. Approve finished goods for dispatch only after quality clearance. 5. Customer Complaint Handling: Investigate quality complaints, identify root causes, and implement corrective actions. Maintain complaint register and coordinate with Sales and Production teams for resolution. 6. Team Management & Training: Lead and train the QC team (executives, inspectors, testers). Conduct internal audits and quality awareness programs for staff. 7. Documentation & Reporting: Maintain records of all inspections, test reports, rejections, and corrective actions. Generate daily, weekly, and monthly QC reports and share with management. Prepare data for audits (internal/external or customer-based). Key Result Areas (KRAs): Reduction in rejection and rework percentage. On-time inspection and quality clearance. Compliance to customer quality standards and zero complaints. Implementation of QC SOPs and training effectiveness. Qualifications & Skills: B.Sc. / B.Tech / Diploma in Paper Technology / Printing / Mechanical / Industrial Engineering. 5–10 years of QC experience in the packaging/corrugated box industry. Sound knowledge of testing equipment (bursting strength tester, GSM tester, moisture meter, etc.). Strong analytical, documentation, and communication skills. Familiarity with ISO, 5S, and other quality systems is a plus. Kindly apply - hr@vidhishapaper.com

Job Summary: The Documentation Engineer will be a key member of the execution team, responsible for managing and maintaining documentation related to installation, commissioning, and qualification of process and utility equipment. This role is ideal for mid-level professionals (3-5 years of experience) looking to advance their expertise in installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) for equipment used in pharmaceutical, chemical, and food processing industries. Key Responsibilities: Prepare and maintain IQ, OQ, PQ documentation for micronizing mills, containment isolators, bulk handling systems, and fluid bed dryers. Ensure documentation aligns with industry GMP, FDA, and other regulatory standards for equipment validation. Support audits by maintaining structured records for qualification processes on day to day basis. Assist in the installation, commissioning, and qualification of high-containment and powder-handling equipment. Coordinate with internal teams and vendors for proper setup and troubleshooting of process equipment, Provide technical support for operation and maintenance of containment solutions. Work with senior engineers to troubleshoot automation systems, PLCs, and electrical components. Analyze equipment efficiency and contribute to continuous improvement initiatives. Maintain electrical consumption reports to optimize operational performance.

Key Responsibilities: 1. Quality Management System (QMS): Establish, implement, and maintain ISO 9001, ISO 14001, ISO 45001, and ISO 50001-compliant QMS. Ensure documentation, internal audits, CAPA, and system updates are regularly reviewed and improved. Ensure compliance with BIS, IEC, and MNRE guidelines. 2. Quality Assurance & Control: Define quality parameters and inspection plans for raw materials (glass, EVA, backsheet, cells), in-process components, and finished modules. Supervise QA/QC operations across all stages incoming material inspection, in-line process checks, and final testing. Manage electroluminescence (EL), IV testing, Hi-pot, insulation resistance (IR), and thermal cycle evaluations. 3. Team Management: Lead and mentor a team of quality engineers, inspectors, and lab technicians. Develop training programs to ensure quality competency at all levels. 4. Vendor Quality Management: Evaluate and approve suppliers based on quality systems, certifications, and performance. Perform supplier audits and support corrective actions for non-conforming materials. 5. Product Certifications & Audit Readiness: Manage third-party certifications (IEC 61215, 61730, BIS, CE, UL, etc.). Coordinate with external labs and certification bodies for new product certifications. Ensure readiness for customer and third-party audits. 6. Root Cause Analysis & Continuous Improvement: Lead investigations into product and process non-conformities. Use tools like 8D, Fishbone, FMEA, and 5 Why analysis for root cause and corrective actions. Implement Lean Six Sigma practices to enhance yield and reduce defects. 7. Customer Interface: Handle customer complaints and quality-related feedback. Support pre-shipment inspections and customer visits. Provide technical documentation and assurance reports.

As an experienced professional with over 3 years of experience in Computer System Validation (CSV) and IT quality assurance within regulated industries such as pharmaceuticals, biotechnology, or medical devices, you will be responsible for developing, executing, and documenting CSV protocols and reports for both new and existing computer systems and software applications. Conducting risk assessments and gap analyses will be a key part of your role to identify potential quality issues and implement necessary corrective actions. Your responsibilities will also include developing and maintaining quality documentation, such as Standard Operating Procedures (SOPs), validation plans, test cases, and reports. You will actively participate in the selection, implementation, and qualification of new IT systems and software, while providing training and guidance to users on CSV and IT quality best practices. Collaboration with cross-functional teams, including IT, engineering, and manufacturing, will be essential to ensure compliance with regulatory requirements. Staying informed about industry best practices and regulatory changes related to CSV and IT quality will be crucial in this role. Additionally, you will be involved in performing internal audits and supporting external audits related to CSV and IT quality. To be successful in this position, you should hold a Bachelor's degree in a related field and possess a deep understanding of GxP regulations, such as 21 CFR Part 11 and Annex 11, along with industry best practices for CSV. Experience with software development lifecycle (SDLC) methodologies and quality management systems (QMS) is required. Excellent written and verbal communication skills are essential, as you will be expected to effectively communicate technical information to both technical and non-technical audiences. Strong analytical and problem-solving skills are also important for this role. The ability to work independently as well as part of a team is necessary to excel in this position. If you meet these qualifications and are interested in this opportunity, please share your updated resume with ruchita.parsekar@e-stonetech.com.,

Actively monitoring and ensuring the quality of products being assembled on a production line by performing regular inspections, identifying defects, implementing corrective actions, and collaborating with production teams to maintain high quality Required Candidate profile Candidate have Good Expereince in Assembly line Either Genset industry Interested Candidates can send their resume on hdinavdeep@gmail.com

Role & responsibilities Lead and manage Incoming (IQC), In-Process (PQC), and Final Quality Control (FQC) processes. Interface with customers, vendors, and cross-functional teams for quality audits, inspections, and approvals. Champion Root Cause Analysis (YY analysis) and drive implementation of effective Corrective and Preventive Actions (CAPA). Ensure compliance to Defense and Aerospace quality standards in design, development, and manufacturing stages. Maintain and continuously improve QMS documentation including SOPs, work instructions, inspection reports, and quality plans. Lead internal and external quality audits, certifications, and statutory compliance. Facilitate cross-departmental coordination for issue resolution and process improvements. Present quality metrics, dashboards, and improvement initiatives to the Managing Director and Senior leadership. Contribute to product and process improvement initiatives, particularly in projects related to Telescopic Masts, Positioners, Tripods, and Power Electronics. Key Skills and Competencies: - Strong understanding of Ok-Ok analysis, and critical inspection points. Solid grasp of ISO/AS9100, ISO 9001 , and other relevant Defense/Aerospace Quality Systems. Proficiency in technical documentation, SOP creation , and QMS tools. Excellent communication, presentation , and stakeholder management skills. Hands-on experience with machining, sheet metal, electronic assembly, and system integration is preferred. Familiarity with defense and Aerospace manufacturing protocols, audit processes , and engineering documentation standards . Desired Candidate Profile: 15+ years of progressive experience in Quality Assurance & Control in Aerospace or Defense manufacturing . Demonstrated capability in leading quality functions , including audits, documentation, and compliance. Experience working directly with customers, OEMs, and defense procurement teams . Should be self-driven, detail-oriented, and possess strong problem-solving and analytical skills.

Role & responsibilities * Creating and maintaining quality control processes, policies, and standards. * Tracking and analyzing quality control data to identify trends, root causes, and areas for improvement. * Supervising and mentoring quality control personnel, providing guidance and support. Working with various teams, departments, and stakeholders to align quality control efforts with business objectives. * Identifying opportunities to enhance product quality and production efficiency. * Maintaining accurate and up-to-date quality control documentation. Preferred candidate profile 10-15 years of experience in the valves/fittings industry, preferably with ADNOC, ARAMCO, KOC, etc.

Build Con is seeking a highly experienced and meticulous Head of Quality Control to lead the quality assurance and control operations at our Ready Mix Concrete (RMC) plant in Dombivli. This role is pivotal in ensuring that all concrete produced meets the highest standards of quality, adhering to IS codes, client requirements, and statutory regulations. Key Responsibilities: Lead and manage the entire Quality Control (QC) function of the RMC plant. Develop, implement, and monitor concrete mix designs in line with IS standards and project specifications. Oversee routine testing of raw materials (aggregates, cement, admixtures, water) and finished concrete to ensure consistency and compliance. Review and approve daily batch reports, cube test results, and all related quality documentation. Identify, analyze, and resolve quality-related issues efficiently to prevent operational disruptions. Ensure the calibration, maintenance, and proper functioning of all laboratory equipment and testing instruments. Maintain comprehensive records of test reports, mix designs, and quality audits. Collaborate with site engineers, clients, and project teams to address concrete performance and quality concerns. Implement corrective and preventive actions for any identified non-conformities. Supervise, guide, and develop the QC team, promoting a strong culture of quality awareness and continuous improvement. Ensure compliance with safety, environmental, and regulatory guidelines in all QC operations. Candidate Profile: Degree or Diploma in Civil Engineering / Materials Engineering. Minimum 7 years of experience in Quality Control operations, preferably in RMC plants or concrete batching facilities. In-depth knowledge of relevant IS codes and concrete material testing procedures. Proficient in concrete mix design, laboratory management, and quality control systems. Strong leadership, problem-solving, and decision-making abilities. Ability to manage teams effectively and work under tight project deadlines. Familiarity with batching software and reporting tools is an added advantage. Candidates based in or willing to relocate to Dombivli, Thane are preferred. Job Type: Full-time Benefits: Provident Fund Schedule: Day shift Night shift Work Location: In person,

Maintain compliance with medical textile standards. Coordinate with production to maintain product quality. Train workers on hygiene, GMP, and quality SOPs. Good understanding of medical garment standards. Attention to documentation.

1. Looking for Graduate Engineer with 6-8 years of experience in QA department of an engineering or FMCG company. 2. Shall be well versed with ISO 9001, ISO45001 and willing to take responsibility for setting up the QMS. 3.Person possessing knowledge about TQM with experience in implementing POKA-YOKE is preferred. 4. Should have experience of documentation of audit process.

1.Responsible for Leading the Quality function and day to day In-process Quality verification with consistent result both in terms of Quality and Quantity to meet daily plant output / customer requirements. 2. Performing in-process quality inspection for accuracy, specification parameters and workmanship. Develop and implement best quality processes in production 3. Tabulate and document data relating to products, processes, materials, its qualities, and reliabilities 4. Train staff, technicians, and professionals on the aspects of quality control activities. 5. Troubleshoot and resolve problems relating to quality using quality tools (DMAIC, 8D, 4Q, PDCA etc.) Capture and analysis of COPQ in order to achieve savings. 2. Conducting regular Inspections and Audits to assess product quality and compliance with established standards 3. Collaborating with production teams to Identify areas for improvement and develop solutions to address quality issues. 4. Ensuring that all quality-related processes comply with local and international regulations and standards 5. Providing training and support to production teams to improve their quality control skills and knowledge 6. Reviewing customer feedback and using this information to identify areas for improvement. 7. Support during Customer Inspections, QA drafting and approvals etc. Implementing Poka-Yoke wherever possible to prevent quality errors and improve safety level. 8. Support and lead continuous improvement programs, problem solving and process improvement activities 9. Adhere to QMS, other company policies and procedures & Quality Documentation Control 10. Strong Technical know-how about the Process flow. KAIZEN & ISO- 9001 and 14001,45001 Documentation. 11. Strong Knowledge about the Corrective Action Plan (8D), Continual Process Improvement 12. Shows moral courage, openness and honesty in all dealings. Good communication and interpersonal skill 13. Ability to work in a diverse and dynamic environment Skills : Good Communication Good Organization & Prioritization

About the Company Boon Management Consultants PVT. LTD (BMCPL): Boon Management Consultants Pvt. Ltd. (BMCPL) is a consultancy organization (Incorporated in 2005) that specializes in providing services for improvement of systems including capacity building, implementation of lean tools, ZED Consultancy etc. BMCPL is providing consultancy and training services to its clients all over India through our consultants located in pan India. Besides many private and services sector clients , we are providing services to government/semi-government organizations. Some of our government clients are 33 ZILLA PARISHADS, RURAL DEVELOPMENT DEPARTMENT- GOVERNMENT OF MAHARASHTRA, OFFICE OF GOVERNOR OF MAHARASHTRA, etc. For the ZILLA parishad project done by us, RURAL DEVELOPMENT DEPARTMENT (RDD) has won National Award. Ministry of MSME, GOI (MoMSME), has selected Quality Council of India (QCI) which is an autonomous body under Govt. of India for implementing and Monitoring ZED and MCLS scheme across India. QCI has selected BMCPL as a ZED consulting organization and also for MCLS consulting organization for pan India operations. Job description – Senior Consultant (Office) Remuneration :- 35,000 to 50,000 per month + Performance incentives Job Type: Full-time, Permanent Education: ( Any of the following) 1. Any Gradutate with knowledge of ISO consultancy/ISO Auditing/ Quality Related fields 2. Any Graduate with minimum 8 years industrial experience in manufacturing. 3. Any Diploma with 10 years industrial experience in manufacturing 4. Any BE/BTech with 8 years industrial experience in manufacturing 5. Knowledge of ISO &/or Lean tools implementation/Documentation/ Consultancy/Systems/Quality related fields shall get additional weightage 6. Probation: - You shall be on a probation for a period of Three (3) months. After probation, depending upon your performance you can get confirmation letter or your probation can be extended/terminated. 7. Training : - a. You shall be trained and guided to become a national level ZED consultant after which you shall be able to take up ZED Consultancy projects. b. If you are eligible, then you shall be trained and guided to become a national level MCLS Consultant after which you shall be able to provide MCLS Consultancy. c. You shall be given training on online QC checks, assessments and all related works which are required for you to handle the required processes independently. d. You shall be given training on ISO 9001/14001/45001 implementation and assessment. e. You shall be trained and guided on ISO 17021 after which you shall accompany our team in witness/office assessments as required by the company. You shall be trained thoroughly before being asked to face audits independently. f. You shall be trained on handling different ZED/MCLS/ISO operations depending on your eligibility and requirement of the company after which you would be required to give online guidance/ trainings to our team pan India. g. Depending upon your performance, dedication, ability to build and handle a team you may be offered a chance to head an operation and earn extra monitoring incentive as per company norms. 8. Roles and Responsibilities:- a. You shall be required to come to our office 6 days a week( Monday to Saturday). b. You shall be required to do a minimum of 5 online assessments per day (100 per month), which can be done from office or home. One assessment requires 15 to 20 minutes on average. c. You shall be required to provide online support/ training to our Pan India team on the topics related to ZED/MCLS/ISO for which we shall train you adequately. d. Once you get the required certifications, To enhance your implementation skills and keep them updated our company may give you field consultancy work for few days in a month. For doing field work you shall be given additional incentive depending upon your efficiency and quality of work. In rare cases, If outstation travel would be required then extra travel and stay accommodation shall be provided by the company. e. You shall be required to prepare necessary MIS and submit them to director weekly/monthly depending on the importance of the operation. f. TDS shall be deducted as applicable for which you shall receive proof from the company and can claim from GOI at the end of the year through your CA. 9. RETAINER-SHIP INCENTIVE shall be given to SENIOR CONSULTANT depending upon his ZED/MCLS/ISO performance and points achieved by him as per the details given in annexure. Perks and Benefits: 1. Cell phone reimbursement 2. Internet reimbursement 3. Performance incentives after field works starts Place of Posting: At our office located in Ithink business park by Lodha, opposite to Xperia mall, Dombivali East - 421204 Schedule : Monday to Saturday

Monitor and control daily extrusion press operations (billet loading, die setup, extrusion, quenching, etc.). Ensure execution of the production plan to meet quantity, quality, and delivery targets. Minimize press downtime and improve overall equipment effectiveness (OEE). Maintain and monitor key process parameters (temperature, speed, pressure, billet length, etc.). Identify process inefficiencies and work with cross-functional teams to improve cycle times and yield. Implement lean manufacturing and 5S practices on the shop floor. Supervise operators and shift technicians; assign tasks and ensure safe working practices. Conduct regular shift meetings and ensure proper handovers between shifts. Train the team in extrusion best practices and standard operating procedures (SOPs). Ensure products meet customer specifications and quality standards. Work closely with the QA/QC team to address non-conformities and reduce rejection rates. Maintain production and quality documentation, including logbooks and traceability records. Identify and troubleshoot issues related to die setup, billet quality, ram pressure, and extrusion defects. Coordinate with maintenance for planned and unplanned shutdowns. Monitor die life and recommend die reconditioning or replacement as needed. Enforce safety protocols and promote a culture of safe working on the shop floor. Ensure proper handling of high-temperature materials, hydraulic systems, and press-related equipment.

About the role: The Proposal, Budget and Contracts Associate is responsible for the development and preparation of proposals, budgets and contracts for new business. The PBC Associate will be accountable for generating high quality and timely proposals, budgets and contracts. PBC Associates work closely with the Business Development team and Projects Managers to ensure high quality documents are delivered according to client expected timelines. Responsibilities: Develop proposal: Prepare high quality proposals and presentation materials. Collate required content and finalize proposal (involves substantive editing & drafting to ensure readability, consistency in formatting to ensure that proposals accurately reflect customers requirements and is consistent with Novotech branding guidelines). Ensure proposal templates remain relevant and compliant and of a high visual standard. Research, compile and present statistics and company information. Develop budget: Prepare budget for projects based on client information provided to schedule timeframe. Prepare other budgets elements (client mapping etc.) as required to timeframes. Liaise with vendors to obtain quotations. Develop Contracts: Prepare all new client contracts and execute in accordance with agreed timeframes and guidance. Obtain appropriate format of Budget for inclusion in contracts. Contracts executed in accordance with Novotech Contract Review SOP. Follow Start Up Work Authorization process to activate project for handover to Operations team. Contact vendors and obtain quotes. Contact vendors for quotes based on protocol and vendor lists. Engage Operation team as required for assistance. Other: Understand the responsibilities of Novotech as a service provider in the pharmaceutical industry and ensure all communication with external parties is presented in a positive and professional manner. Attend calls with internal teams and clients in development of opportunity documents. Maintain and update opportunity status within Salesforce. Maintain contracts records in Salesforce and SharePoint. Minimum Qualifications & Experience: Graduate in a clinical or life sciences related field. Relevant experience/qualifications in allied professions may also be considered. At least three years experience within the pharmaceutical industry. Previous experience working directly with clients will be highly regarded. Must be able to communicate clearly, able to priorities and meet deadlines. Must have advanced Microsoft office capabilities, specifically Excel, Word and PowerPoint. Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect. Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs. We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities. We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to contacting you regarding your application. About the role: The Proposal, Budget and Contracts Associate is responsible for the development and preparation of proposals, budgets and contracts for new business. The PBC Associate will be accountable for generating high quality and timely proposals, budgets and contracts. PBC Associates work closely with the Business Development team and Projects Managers to ensure high quality documents are delivered according to client expected timelines. Responsibilities: Develop proposal: Prepare high quality proposals and presentation materials. Collate required content and finalize proposal (involves substantive editing & drafting to ensure readability, consistency in formatting to ensure that proposals accurately reflect customers requirements and is consistent with Novotech branding guidelines). Ensure proposal templates remain relevant and compliant and of a high visual standard. Research, compile and present statistics and company information. Develop budget: Prepare budget for projects based on client information provided to schedule timeframe. Prepare other budgets elements (client mapping etc.) as required to timeframes. Liaise with vendors to obtain quotations. Develop Contracts: Prepare all new client contracts and execute in accordance with agreed timeframes and guidance. Obtain appropriate format of Budget for inclusion in contracts. Contracts executed in accordance with Novotech Contract Review SOP. Follow Start Up Work Authorization process to activate project for handover to Operations team. Contact vendors and obtain quotes. Contact vendors for quotes based on protocol and vendor lists. Engage Operation team as required for assistance. Other: Understand the responsibilities of Novotech as a service provider in the pharmaceutical industry and ensure all communication with external parties is presented in a positive and professional manner. Attend calls with internal teams and clients in development of opportunity documents. Maintain and update opportunity status within Salesforce. Maintain contracts records in Salesforce and SharePoint. Minimum Qualifications & Experience: Graduate in a clinical or life sciences related field. Relevant experience/qualifications in allied professions may also be considered. At least three years experience within the pharmaceutical industry. Previous experience working directly with clients will be highly regarded. Must be able to communicate clearly, able to priorities and meet deadlines. Must have advanced Microsoft office capabilities, specifically Excel, Word and PowerPoint. Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect. Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs. We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities. We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to contacting you regarding your application.

About the role: The Proposal, Budget and Contracts Associate is responsible for the development and preparation of proposals, budgets and contracts for new business. The PBC Associate will be accountable for generating high quality and timely proposals, budgets and contracts. PBC Associates work closely with the Business Development team and Projects Managers to ensure high quality documents are delivered according to client expected timelines. Responsibilities: Develop proposal: Prepare high quality proposals and presentation materials. Collate required content and finalize proposal (involves substantive editing & drafting to ensure readability, consistency in formatting to ensure that proposals accurately reflect customers requirements and is consistent with Novotech branding guidelines). Ensure proposal templates remain relevant and compliant and of a high visual standard. Research, compile and present statistics and company information. Develop budget: Prepare budget for projects based on client information provided to schedule timeframe. Prepare other budgets elements (client mapping etc.) as required to timeframes. Liaise with vendors to obtain quotations. Develop Contracts: Prepare all new client contracts and execute in accordance with agreed timeframes and guidance. Obtain appropriate format of Budget for inclusion in contracts. Contracts executed in accordance with Novotech Contract Review SOP. Follow Start Up Work Authorization process to activate project for handover to Operations team. Contact vendors and obtain quotes. Contact vendors for quotes based on protocol and vendor lists. Engage Operation team as required for assistance. Other: Understand the responsibilities of Novotech as a service provider in the pharmaceutical industry and ensure all communication with external parties is presented in a positive and professional manner. Attend calls with internal teams and clients in development of opportunity documents. Maintain and update opportunity status within Salesforce. Maintain contracts records in Salesforce and SharePoint. Minimum Qualifications & Experience: Graduate in a clinical or life sciences related field. Relevant experience/qualifications in allied professions may also be considered. At least three years experience within the pharmaceutical industry. Previous experience working directly with clients will be highly regarded. Must be able to communicate clearly, able to priorities and meet deadlines. Must have advanced Microsoft office capabilities, specifically Excel, Word and PowerPoint.

Roles and Responsibilities Develop and implement quality management systems (QMS) according to ISO standards, ensuring compliance with customer requirements. Conduct internal audits, identify areas for improvement, and implement corrective actions to maintain high-quality products and services. Collaborate with cross-functional teams to develop process documentation, including PPAPs, technical specifications, and quality manuals. Ensure timely completion of customer audits by providing necessary documents and support. Maintain accurate records of QMS activities, such as audit reports, corrective action plans, and training records. Desired Candidate Profile 6-10 years of experience in a similar role within the automotive industry or related field. Strong understanding of IATF 16949 standard; certification preferred. Experience with TS/ISO documentation processes; ability to create clear documentation using MS Office tools (Word). Excellent communication skills; ability to work effectively with diverse stakeholders at all levels.

Perform inspections of 3D printed and assembled parts,ensuring quality standards.Work with production/design teams to resolve issues,ensure specifications are met.Basic 3D printing knowledge, measuring tools handling,QA documentation skills required Food allowance Provident fund Health insurance Annual bonus

As an experienced professional with over 3 years of experience in Computer Systems Validation (CSV) and IT quality assurance within regulated industries such as pharmaceuticals, biotechnology, and medical devices, you will be responsible for the following key tasks: - Developing, executing, and documenting CSV protocols and reports for both new and existing computer systems and software applications. - Conducting risk assessments and gap analyses to identify potential quality issues and implementing corrective actions as necessary. - Developing and maintaining quality documentation including Standard Operating Procedures (SOPs), validation plans, test cases, and reports. - Participating in the selection, implementation, and qualification of new IT systems and software. - Providing training and guidance to users on CSV and IT quality best practices. - Collaborating with cross-functional teams (e.g., IT, engineering, manufacturing) to ensure compliance with regulatory requirements. - Staying updated on industry best practices and regulatory changes related to CSV and IT quality. - Performing internal audits and supporting external audits related to CSV and IT quality. To be successful in this role, you should possess the following qualifications: - A Bachelor's degree in a related field. - 3-4 years of experience in CSV and IT quality assurance within regulated industries. - Strong understanding of GxP regulations such as 21 CFR Part 11, Annex 11, and industry best practices for CSV. - Experience with Software Development Lifecycle (SDLC) methodologies and Quality Management Systems (QMS). - Excellent written and verbal communication skills, with the ability to effectively communicate technical information to both technical and non-technical audiences. - Strong analytical and problem-solving skills. - Ability to work both independently and as part of a team. If you meet the qualifications and are looking for a challenging opportunity to further develop your skills in CSV and IT quality assurance, we encourage you to share your updated resume with us at ruchita.parsekar@e-stonetech.com.,