2371 Qms Jobs - Page 22

Key Responsibilities: Administer document and record control systems, ensuring version control, traceability, timely reviews, and overall compliance. Perform and document software tool validations and revalidations, ensuring alignment with relevant standards. Support supplier selection and ongoing monitoring, including maintaining relevant documentation and ensuring supplier compliance. Monitor regulatory developments (e.g. AI Act, GDPR), assess gaps, and implement required changes in the QMS. Draft, revise, and maintain procedures and work instructions based on regulatory or process changes. Prepare input for periodic management reviews, including KPIs, audit outcomes, and improvement actions. Support internal audits and coordinate evidence collection and follow-up actions. Proactively identify and drive opportunities for quality improvement or operational efficiency. Qualifications: 3+ years of hands-on experience in a quality or compliance role within a regulated industry (medical devices, pharma, health tech, etc.). Strong working knowledge of at least one management system (e.g. ISO 13485, ISO 27001, or ISO 9001). Excellent English communication skills (written and verbal); all documentation and communication is in English. Experience with documentation systems, change management, and audit readiness. Comfortable working independently and taking initiative in a remote setup. Nice-to-Have Certifications (not required): ISO Lead Auditor (9001 / 13485 / 27001) Regulatory Affairs Certification (RAC) or similar Computer System Validation (CSV) training Key Competencies: Excellent written and verbal English communicates clearly and professionally with international clients, both in documentation and direct interactions. Strong ownership mindset – proactively identifies tasks, follows through independently, and flags issues without needing micromanagement. Regulatory awareness and adaptability – keeps up with evolving standards (e.g., ISO updates, AI Act, MDR/IVDR) and translates them into practical system improvements. Clear and concise technical writing – able to draft and revise SOPs, validation reports, and audit evidence to meet compliance requirements. Process improvement orientation – continuously looks for ways to streamline or strengthen compliance workflows. Effective remote collaboration – comfortable in asynchronous, cross-border work environments and knows when to escalate or ask for input. Hands-on tool proficiency – experienced with document control systems (EDMS), QMS platforms, and validation or audit tracking tools.

-Conduct Sampling of Raw materials as per sampling protocol. -Maintain calibration records and instrument logbooks. -Perform testing/analysis of raw materials. -Doing QMS

Ensure all quality control procedures are documented and adhered to throughout the manufacturing process. Lead continuous improvement initiatives to enhance product quality and operational efficiency. Manage, mentor, and develop the quality control team, including hiring, training, performance evaluations, and career development. Ensure compliance with relevant industry standards, regulatory requirements, and customer specifications. Maintain up-to-date knowledge of industry standards, regulatory requirements, and best practices. Oversee and coordinate quality control testing and inspection processes, including raw material, in-process, and final product inspections. Collaborate with customers to understand their quality requirements and address quality-related concerns. Manage customer complaints and ensure timely resolution through effective problem-solving and communication. Creation and implementation of quality concepts, work and process instructions Drive completion of APQP and PPAP processes to obtain customer approval. FMEA (Failure Mode and Effects Analysis), and Control Plan processes. Develop and maintain strong trust-based relationships with customers, serving as the main point of contact for all quality-related matters. Quality Certification will be an Added Advantage Knowledge of Forging industry Candidate Should be Willing to Relocate to Shirdi as factory Location is Shirdi.

Lead Shift Production focusing on; Sampling Orders creation Production plan execution Manpower allocation Problem analysis & Counter measure Production MIS OEE aderance-90% Schedule adherance-100% Operator productivity asper target Cost reduction Required Candidate profile DME/BE 3+yrs exp into PRODUCTION with AUTO/ENGG unit leading 6-10 TM/Operators Strong exp in Team Mgmt, Cost Reduction, QMS, HSE, 5S, OEE, QMS, Maintenance of Coaters, big tool blasting machines etc Perks and benefits Excellent Perks. Send CV recruiter@adonisstaff.in

Role & responsibilities 1)Strategic Process Optimization: Diagnose performance gap across core value chain (Manufacturing, supply chain , Quality , regulatory)and identify value leakages Liaison with site Business excellence team and setup monitoring mechanisms for key project /Initiatives Partner with functional leaders to drive cost, quality and service level improvement Digitization and automation enablement: Collaborate with IT / Tech teams to identify use cases of digital intervention in manufacturing R&D and supply chain digitization 2)Performance Management system: Design and Implement KPI dashboards with real time visibility into key operational metrics Establish structured performance review mechanism (Daily tier reviews, monthly ops scorecards, etc) 3)Cross Functional Execution: Align improvement initiatives with corporate strategy and ensure cross functional engagement. Lead or co-lead high -impact special project, such as plant productivity programs, cost rationalization or new tech transfer readiness Provide structured problem-solving support to senior leadership on complex operational issues 4)Success Metrics: Net saving from OpEx initiatives (Direct and Indirect) Validate through finance % of strategic operational initiatives delivered on time and within scope 9Linked to transformation road mad) Improvement in service ability at the enterprise level(Supply chain + Production + customer service ) Adoption rate of new digital tools / platforms %Of core business process digitized /standardized Interested candidate can drop their resume on renuka.u@encubeethicals.com

Candidate should have knowledge of handling and troubleshooting the sophisticated Analytical Instruments like HPLC, GC, IR, UV, KF ETC . Also He should be able to work, adopt and guide subordinates in following Good Laboratory Practices. He should be well versed with various regulatory & Statutory requirements. Candidate Profile: Should have minimum Four years experience. He should be able to work with the team and be willing to take initiative & challenge for completing the task assigned.

Candidate should be able to achieve the organizational goal in maintaining the Quality Management system of API industry. He should be able to execute various function QMS like CAPA, Deviation, CC, Risk assessment ETC Candidate Profile: Should have minimum Two years experience. He should be able to work with the team and be willing to take initiative & challenge for completing the task timely

Role & responsibilities Financial Leadership Full ownership of P&L and financial stewardship for the Indian operation. Lead annual budgeting, forecasting, and financial planning in alignment with group goals. Ensure compliance with Indian accounting standards and global GAAP, partnering with third-party auditors and corporate finance. Maintain strong financial controls, reporting discipline, and audit readiness. Sales & Business Development Develop and execute a local sales strategy to grow domestic market share and support global customer relationships. Expand business with existing OEM clients while pursuing new opportunities. Ensure efficient and professional handling of RFQs and customer communication. Deliver consistent sales reporting and performance tracking. Human Resources Leadership Drive a culture of performance, accountability, and compliance through best-practice HR leadership. Oversee talent planning, capacity alignment, and compliance with corporate and local labor laws. Manage performance cycles, compensation planning, and employee development programs. Support a safe, engaged, and inclusive workplace culture. Operational Oversight Work closely with GM Operations to provide strategic direction and accountability for production, quality, engineering, and procurement functions. Ensure timely delivery, product quality, cost optimization, and continuous process improvement. Monitor operational KPIs, manage labor relations, and uphold safety and compliance standards. Maintain effective communication and reporting systems across departments. Preferred candidate profile Proven executive experience (20+ years) with a track record of building relationships/business with multi-national customers, preferably in manufacturing, automotive, or industrial sectors. Strong financial acumen and demonstrated P&L ownership. Deep understanding of sales strategy, customer relationship management, and market development. Hands-on experience managing HR strategy and compliance in India. Preferred Qualifications: Experience in a global manufacturing environment with exposure to OEM customers. Track record of driving operational excellence and cultural transformation. Engineering or business degree; MBA or related advanced degree is an asset. Personal Attributes: Strategic thinker with hands-on leadership style. Excellent interpersonal, negotiation, and communication skills. High integrity, results-oriented, and culturally agile.

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.,

As the Head of Production, you will play a crucial role in the planning, coordination, and control of manufacturing processes, focusing on Factory Layout and Production Layout. Your responsibilities will include collaborating with internal and external stakeholders to provide technical support, ensuring the production of top-notch products and adherence to best business practices. You will lead and manage teams and projects across the organization, offering clear direction, inspiration, and guidance to drive excellence and motivate staff towards success. Your primary responsibilities will involve designing and validating factory layout and production layout, developing engineering bills of process and resources, and planning manufacturing processes for assembly. You will be tasked with conducting capacity and cycle time calculations, as well as planning and designing equipment, tooling, jigs, and fixtures. Additionally, you will be involved in supplier qualification processes, developing quality metrics, and performing various analyses to ensure optimal performance and efficiency. Furthermore, you will be responsible for planning and executing MES architecture in line with ISA95 standards and implementing Industry 4.0 strategies. Managing factory operations, ensuring compliance with regulatory requirements, conducting safety and risk analyses, and implementing ISO standards will also be part of your role. To excel in this position, you should hold a BE/ME degree in Mechanical, Automobile, or Industrial Engineering, with a strong background in Factory and Layout planning. Experience in automated and manual assembly lines, tool design, manufacturing processes, and knowledge of quality standards are essential. Familiarity with GD&T, tolerance stack-up analysis, APQP, DFMEA, PFMEA, as well as PLM, ERP, and ISO standards is required. Knowledge of CMM, Blue light scanning, and I4.0 principles will be advantageous. Key competencies for success in this role include being results-oriented, self-motivated, and possessing a problem-solving attitude. Integrity, teamwork, and a sense of ownership are critical traits for this position, as is a commitment to driving performance and contributing to the organization's success.,

The Data Migration Lead Engineer will play a vital role in overseeing and executing the migration of data to Veeva Vault. In this position, you will be responsible for ensuring data integrity and quality throughout the migration process, as well as developing effective strategies for mapping data from various legacy systems to Veeva Vault. Your key responsibilities will include developing and leading data migration strategies specifically for Veeva Vault from QMS, DMS, and LMS systems. You will be required to manage the end-to-end data migration processes, ensuring high quality and integrity before and after migration. Precision in mapping master data elements from legacy systems to the target systems will be crucial for successful execution. As the Data Migration Lead Engineer, you will also be tasked with managing and mentoring migration teams to ensure a seamless execution of the data migration process. Compliance with data migration standards and best practices will be a key focus area to maintain the quality and integrity of the migrated data. To excel in this role, you should have proven experience in migrating data to Veeva Vault from a diverse range of QMS, DMS, and LMS systems. Expertise in developing and executing data migration strategies, as well as strong skills in mapping master data elements across different systems, will be essential. Additionally, leadership experience and the ability to manage teams effectively are prerequisites for this position. A deep understanding of data integrity and quality assurance processes will be beneficial for ensuring the successful and accurate migration of data to Veeva Vault.,

The key deliverables for this role include managing Cost of Poor Quality (COPQ), Call Rate & Return Reduction, ensuring flawless New Launches of Outgoing Products, enhancing Quality Management Systems (QMS), improving Radar Score, developing Supplier Upgradation Roadmap by enhancing Quality Maturity Progression Score, reducing Tier 2 Supplier PPM, improving Rolling Throughput Yield, and building competency of the team at the Supplier end through trainings. Your duties and responsibilities will involve integrating with various functions to ensure flawless New Product Introduction, meeting quality deliverables at each gate through Quality Risk Assessment sign off, tracker & objective targets, reviewing and ensuring validation compliance, engaging suppliers on PPAP and run@rate delivery, executing APQP on Finished Goods bought out parts, establishing process controls and critical touch points at the supplier end, reviewing the performance of new products for the first 6 months post-launch, driving Built-in Quality through identification of Critical stations/parameters, ensuring Touch & Feel of the product meets Global standards, developing suppliers" quality systems as per Havells expectations, mitigating risks through Change Management/validation, supporting problem resolution, setting up immediate containment, and raising quality concerns. To qualify for this position, you should hold a BE/B.Tech degree with 8-12 years of experience. Additional knowledge of Quality Management Systems (QMS), Integrated Management Systems (IMS), Change Management, Six Sigma, and Design of Experiments (DOE) will be preferred. Mandatory experience in Water Pumps is required. If you are interested in this opportunity, please share your CV at varsha.tomar@havells.com with the same subject line and include the following details: Current CTC, Expected CTC, and Notice period.,

As a Mechanical Product Designer, your primary responsibility will be to design and enhance mechanical products using Autodesk Inventor while ensuring manufacturability and compliance with industry standards. You will play a crucial role in interpreting customer requirements, estimating project efforts, and tracking schedules. Additionally, you will be involved in analyzing and improving product design drawings and engineering data, as well as identifying opportunities for process enhancements. Collaboration with cross-functional teams and providing regular project updates will be essential aspects of your role. You will be expected to perform design verification, calculations, and GD&T according to ASME Y14.5 standards. Your proficiency in creating detailed drawings and technical documentation will be crucial, along with your expertise in machine design, gear and gearbox selection, bearing housing, fasteners, and industrial product development. A Bachelor's degree in Mechanical or Production Engineering with 6+ years of experience or a Diploma with 14+ years of experience is required for this position. You should possess strong skills in manual calculations for design verification, as well as proficiency in top-down and bottom-up assembly methods. Expertise in SolidWorks for modeling and design work is mandatory, along with familiarity with AutoCAD/Inventor and PLM/PDM systems. Knowledge of industry standards such as EN, DIN, ISO, and ASME compliance is necessary. Soft skills like strong team collaboration, effective customer communication, and active participation in design reviews are also important for success in this role. Desired skills include experience with Evaporators, Plate Heat Exchangers, and Cooling Systems, hands-on experience with Autodesk Inventor, and the ability to introduce automation in 3D modeling and drafting processes. Exposure to North American/European clients and projects, as well as knowledge of additional CAD tools and Quality Management Systems, will be advantageous.,

Whacked Out Media is looking for Audience Developer to join our dynamic team and embark on a rewarding career journey. Design and implement audience segmentation strategies to drive targeted marketing campaigns across digital platforms. Collaborate with marketing, data analytics, and content teams to define high - impact audience segments and optimize campaign performance. Use tools like CDPs, CRMs, and DMPs to create, analyze, and refine audience data across channels. Build automated workflows for audience creation and activation in platforms like Google Ads, Meta, and programmatic DSPs. Monitor user behavior across web, app, and email touchpoints to tailor messaging and boost personalization. A/B test different audience cohorts to improve conversion rates and ROI. Ensure compliance with data privacy regulations such as GDPR and CCPA in all targeting and segmentation practices. Provide audience insights to creative and strategy teams to inform messaging, UX, and customer journey strategies.

Kalol Institute & Research Center is looking for QA & Pharma. Chemist to join our dynamic team and embark on a rewarding career journey. Dispense prescription medications and other health - related products to customers. Maintain accurate and complete records of customer transactions and medications dispensed. Ensure that medications are stored and dispensed in compliance with all applicable laws and regulations. Excellent customer service skills. Good organizational and communication skills.

JOB PROFILE OF SR. TECHNICAL OFFICER-QUALITY ASSURANCE MENDINE PHARMACEUTICALS PVT LTD Job Title / Designation- SENIOR TECHNICAL OFFICER - QA Qualifications- M.PHARM Experience- 5 to 6 years experience in QUALITY ASSURANCE Job Objective- The ideal candidate will be responsible for implementing and maintaining quality systems, ensuring compliance with cGMP guidelines, conducting internal audits, reviewing batch records, and supporting regulatory inspections. This role demands strong documentation skills, a sound understanding of pharmaceutical quality standards, and the ability to work collaboratively across departments to uphold product integrity and safety throughout the manufacturing process. Job Responsibilities 1) Quality Risk Management 2) Batch Manufacturing Record preparation 3) Process Validation 4) Packaging Material Specification Preparation 5) APQR 6) Cleaning Validation 7) Regulatory Affairs activity 8) Dossier preparation 9) Application of ONDLS system 10) Form 29 & Form 30 preparation 11) Endorse documents preparation 12) New drug application 13) COPP application in ONDLS.

Job Title: Site Manager Experience: 712 Years Location: AL (Unit -1) Reporting To: Senior Manager / Operations Head Role & responsibilities :- Ensure / Sent daily inspection reports to customer on EOD / next day Morning before 10 am. Ensure that processes needed for the Quality Management System (QMS) are established, implemented and maintained. Report to top management on the performance of the QMS and any need for improvement. Ensure the promotion of awareness of customer requirements throughout the organization. Ensure that the performance of the QMS is reviewed at planned intervals to ensure its continuing suitability, adequacy and effectiveness. This review means assessing opportunities for improvement and the need for changes to the QMS. Ensure that Quality Objectives are set by top management for measuring the performance of the QMS and that these are regularly reviewed. Ensure that all new staff is inducted into the requirements of the QMS related to their own roles and responsibilities. Provide update training as necessary. Ensure that top management undertakes periodic but regular assessments of customersatisfaction and that consequent improvement are identified and implemented. Analyze data on the effectiveness of the QMS and evaluate where continual improvements of the QMS can be made. This shall include data generated as a result of monitoring and measurement and from other relevant sources. Co-ordinate continual improvements of the QMS, ensuring that evidence of corrective and preventive actions taken are recorded and reviewed. Ensure Team leader and Quality inspectors are follow their roles and responsibilities as agreed by top management. Ensure and followed company ethics and integrity to all crown associates inside and outside company. • Crown yearly objective / target should be achieved 100%. Key Skills & Competencies: Strong leadership and team management Deep understanding of QMS and quality assurance principles Excellent communication and customer handling skills Analytical thinking and problem-solving Training and people development Commitment to ethics and integrity Contact HR - 98840 49633 Mail - hr1@crownqualityservices.com

Strong technical understanding of core flow assurance and or process/pipeline simulation technology Thorough working understanding of of OLGA, PVTSim, PIPENET, MULTIFLASH, PIPESIM & SPS softwares Minimum 3 years of experience as Flow Assurance Engineer. Hands on experience of Well modeling, Well start-up, hydrare management study, WAX analysis, sand management, sand erosion, corrosion study, pipeline slugging & mitigation methods,pipeline transient operations like Pigging, turndown, ramp up, blowdown, start-up & shutdown analysis using OLGA Should have experience in handling single phase liquid system for steady state & pressure surge analysis. Should have strong report writing & excellent communication skills Exposure to HYSYS dynamics study is an advantage for topside dynamics simulations as per C&E charts. Candidate should have experience on the preparation of technical proposal for flow assurance study without intervention of Lead consultants Experience in interaction with client and handle project independently without any intervention from senior consultants. Good communication and interpersonal skills B.E/B.Tech/M.E/M.Tech in Chemical or Petroleum Engineering, with a CGPA of 7.0 or 70% marks The Flow Assurance Engineer shall work without supervision, be conversant in flow assurance and/or process/pipeline simulation, and serve as a technical point of contact for the Customer, Contractor(s), Suppliers/Vendors and other internal department(s). Develop work scopes, proposals, and CTRs as required. Independently perform detailed technical work in support of project and study work. Lead big flow assurance projects or individual work scope areas on large projects. Act as Customer Interface as required Prepare project documents and ensure project QA compliance. Support other work as may be required on a time-to-time basis. This may involve studies, development work or other similar work. The engineer shall ensure that they comply with the Company HSE Policy and Quality Management System (QMS). It should be noted that each person has a responsibility for the safety and quality aspects of the work that they undertake. Any questions or concerns relating to HSE and/or the QMS should be brought to the attention of the Project Manager or Operations Supervisor.

External Quality Culture Ensure awareness for quality focus to increase customer satisfaction, particularly in the development process Plan, implement and live Quality culture within Product Line and organization level (Implement the defined processes, improve product quality, initiate process improvements, and drive continuous improvements (CI) in projects) Ensuring compliance (of products) with legal and normative requirements (including tailoring of processes as appropriate) Effectively review product risk management activities (including Risk Analysis, Risk Management Report) Collaborate with onsite teams to keep project teams aligned with headquarters’ expectations Drive best practices within the organization Quality Management Define quality strategy in Quality Management Plan Drive process compliance in the complete lifecycle process of the medical device - starting with product definition till End of Support Act as independent reviewer for design reviews acc to QSR 820.30 (e) with the responsibility of defining and documenting the overall result of the design review. Work with internal delivery team and other functions in order to meet the specified Quality Goals of the project Supporting and consulting of employees in implementing and realizing the processes as well as decision about tailoring of defined processes - both according to the needs of the business and in compliance with statutory requirements Identify opportunities to improve productivity and efficiency with lower costs, reduce non-conformance costs Initiate and moderate the root cause analysis and monitor effective and timely implementation of CAPA Reporting and Coordination Prepare and provide input to the periodic reports as needed by headquarter team Audits and Assessments Conduct / Participate in Internal Audit and External Audits using MDSAP methodology. Coordinate and ensure timely closure of audit findings Qualification Requirements Bachelors or Masters in Engineering / MCA having an excellent academic track record. Proficient in managing Quality of complete Software Medical Device Development lifecycle in distributed international environment. Experienced in latest trends of Software Product Development (e.g. Trunk Based Development, Continuous Delivery (DevOps) etc) Advanced knowledge of quality tools for Metrics data analysis and decision making Advanced computer skills (MS Office tools like Word, Access, Excel, PowerPoint and Outlook) Highly energetic and ”Go-getter” Proven ability to independently plan and successfully execute multiple projects based on business priorities. Display of a high level of critical thinking in bringing successful resolution to high-impact, complex and cross-functional problems is expected. Advanced knowledge of organization's business practices and issues faced and contributions to problem resolution of those issues. Excellent organizational and communication skills (e.g. Moderation, presentation to all levels). Auditor experience in Medical Device area is preferred. 4 - 8 years of successful experience in Quality Management and demonstration of Key Responsibilities and Knowledge as mentioned above. Advanced degree MAY be substituted for experience, where applicable.

- Knowledge of maintaining agricultural produce - To maintain standards and specifications of all raw materials - Vegetables & Fruits and also finished products - To assist in all areas related to product quality including trouble shooting, visiting, production, facilities, designing, training, quality control panel - To provide information that is accurate, reliable and adequate for the intended purpose - Keep the management team apprised of the quality issues - Responsible for inspecting and documenting all incoming fruit, vegetables, packaging materials, and ensure all product quality standards are adhered to. - Perform routine quality and condition inspections on existing inventory to assist in first-in, first-out (FIFO) or worst-in, first-out (WIFO) stock rotation. - Ensure all inbound carrier trailers and materials meet company quality and food safety standards. - Communicate Quality Assurance issues, including defect levels and problem loads, to Sales, Production, and QA managers. - Verify customer specifications, quality requirements of product orders, documentation submitted and approved vendors. - Coordinate inspections - Maintain instruments, records of calibrations, and supplies as needed to meet quality inspection requirements to ensure that company standards are met. - Work closely with Production and Warehouse departments to ensure effective stock rotation to reduce shrinkage. - Maintain daily inbound inspection and defect reports, weekly inbound raw material reports and keeps accurate documentation for food safety purposes. - Responsible for daily sanitation of equipment, and inspect repack products as needed. - Ensure quality of product meets quality standards and communicate any inconsistency to sales, purchasing, management, and quality control department.

Role & responsibilities Role Objective: To support the implementation, monitoring, and continual improvement of quality systems including ISO standards, internal audits, documentation, and regulatory compliance for enhanced operational excellence. ISO Standards Implementation Develop and implement systems aligned with ISO 9001, ISO 14001, ISO 45001, and other relevant standards Conduct gap analyses and prepare action plans for certification readiness Coordinate internal and external audits and manage corrective actions Quality System Development Design and maintain quality manuals, SOPs, work instructions, and process documentation Monitor compliance with regulatory and customer requirements Facilitate root cause analysis and implement preventive measures Training & Awareness Conduct training sessions for employees on ISO standards and quality procedures Promote a culture of quality and continuous improvement across departments Reporting & Documentation Maintain records of audits, non-conformities, CAPAs, and improvement initiatives Prepare reports for management review and certification bodies Cross-Functional Collaboration Work closely with production, HR, safety, and compliance teams to align quality goals Support supplier audits and vendor quality assessments Preferred candidate profile Documentation, auditing, training, problem-solving, stakeholder communication LA in ISO9001, ISO14001 and ISO45001

Strong knowledge of FDA QSR, ISO 13485, EUMDR & regulatory norms. Manage QMS docs, DHFs, CAPAs, audits, suppliers, training & calibration. Support audits, product dev, quality improvements & regulatory compliance. Excellent doc & comm skills needed.Regulatory Compliance: Apply your strong knowledge of FDA QSR, ISO 13485, and EU MDR to ensure all activities meet regulatory norms. QMS Management: Manage essential Quality Management System (QMS) documentation, including Design History Files (DHFs) and Corrective and Preventive Actions (CAPAs). Audits & Reviews: Support internal and external audits, manage supplier qualifications, and oversee training and calibration programs. Cross-functional Support: Provide critical quality support for product development, drive quality improvements, and ensure ongoing regulatory compliance.

Hi All, GE Aerospace is looking for Deputy Engineer - Quality for Pune, Chakan location. Company Overview: Working at GE Aerospace means you are bringing your unique perspective, innovative spirit, drive, and curiosity to a collaborative and diverse team working to advance aerospace for future generations. If you have ideas, we will listen. Join us and see your ideas take flight. Site Overview: Our Multi-modal Manufacturing Facility (MMF) in Pune plays a crucial role in manufacturing key aerospace components, supporting not only Indias defence and commercial sectors but also global aviation supply chains. Our relationships with Indian suppliers, combined with our world-class local facilities and global reach, continue to shape Indias aerospace ecosystem. Role Overview: The position will report to the Quality Engineer / Manager. Should have sound knowledge of FAI preparation and review. Well versed with Net Inspect Portal, eCAV Should have strong drawing, specification interpretation skills. Work closely with manufacturing / production & Quality system teams to develop and implement AS 9100 procedures & systems & support driving end to end production quality flow downs. Willingness to work & get qualified to Cross functional teams & quality cells along with HPT teams for daily analysis of yield improvement , EHS & process improvisation projects. Contribute to continual improvement through audit programs, assessment / of various non-conformances and driving corrective actions identified through Root Cause Analysis. Understanding of site quality QMS procedures & policies. Understanding quality tools related to process yield improvement tools like RCA , KAIZENS , 7 QC tools , Defect Analysis etc. Inspecting production hardware , attending to customer complaint analysis & stock verifications where required. Providing technical analysis and evaluation both manually and automatically to assigned inspection processes. Knowledge on dimensional inspection methodologies. Providing training, and support to shop operations, design and manufacturing to assure effective Quality Assurance Maintaining awareness of the latest inspection techniques & processes and their beneficial and limiting aspects for optimum application Pursuing continuous improvement for quality & cost reductions projects. Actively contributing to non conformance event management & analysis. The Ideal Candidate: Candidate would be responsible for FAI preparation of the aerospace hardware. Aware about AS9100, AS9102, NC, RCCA and QMS requirement Qualifications/Requirements: Diploma in Mechanical Engineering 4 - 7 years of Experience in Production quality. Well versed with usage of Net-inspect and eCAV for FAI submission. Experience in Aviation industry in the fields of aviation quality inspection & product acceptance is added advantage, Working knowledge of AS 9100 and internal requirements. Strong working knowledge of GD&T, drawings & specifications interpretation Preferred Qualifications Working knowledge of AS 9100 and internal requirements Knowledge of AS 9100 or AMS , S1000 / S1002 standards. Knowledge of Basic Lean and Six Sigma Methodology Whether we are manufacturing components for our engines, driving innovation in fuel and noise reduction, or unlocking new opportunities to grow and deliver more productivity our GE Aerospace teams are dedicated and making a global impact. Join us and help move the aerospace industry forward

Dear Candidates, We are seeking a dynamic, results-oriented Senior Production Manager with deep expertise in modern seafood production techniques and quality management systems. The ideal candidate will possess extensive experience in production planning, plant operations, and administrative control within the seafood industry, especially in handling sea-caught shrimp and Vannamei processing . This is a leadership role requiring strong decision-making capabilities, team management, and an in-depth understanding of the seafood processing life cycle, ensuring productivity, compliance, and product excellence. Roles and Responsibilities Lead and manage end-to-end production operations in a seafood processing facility. Develop and implement production plans, schedules, and resource allocation to meet demand forecasts. Oversee the processing of sea-caught shrimp and Vannamei, ensuring high standards of hygiene, quality, and compliance. Implement and monitor quality control (QC) and quality assurance (QA) systems as per industry and export standards. Drive continuous improvement initiatives in processing efficiency, waste reduction, and operational excellence. Coordinate with procurement, logistics, and quality departments to streamline supply chain and inventory management. Provide leadership, mentoring, and performance evaluation to production teams and supervisors. Analyze production data, prepare reports, and provide insights to top management for strategic decision-making. Manage plant infrastructure, machinery maintenance, and upgrades in line with industry standards and automation trends. Desired Candidate Profile A proven track record of 14 to 20+ years in seafood processing, preferably in a senior production or plant management role. Strong understanding of shrimp (sea-caught and Vannamei) processing , freezing, packaging, and export compliance. Hands-on experience with modern seafood production techniques , HACCP, ISO, and other quality certifications. Demonstrated ability to lead teams, make quick and effective decisions, and handle production crises. Excellent planning, coordination, and communication skills. Should be familiar with international seafood export requirements and quality benchmarks. INTERESTED CANDIDATES KINDLY APPLY!!!

We are hiring an experienced Construction Project Manager to lead end-to-end execution of commercial building projects in Pune. This is a site-based role involving complete project lifecycle from planning to handover.