50 Quality System Jobs

As a Drilling Solutions Engineer with NOV in Mumbai, India, your role will involve identifying new opportunities, expanding product development, and maximizing profitability for customer accounts. Here is a breakdown of your key responsibilities: - **Customer Service:** - Maintain good working relationships with customer accounts personnel. - Deliver technology presentations and training sessions. - Monitor customer issues, feedback, and deadlines. - Ensure timely and accurate invoicing according to NOV and local customer legal requirements. - **Sales Support:** - Qualify opportunities and offer insights to maximize revenue. - Create technical evaluations and product recommendations. - Suppo...

You should have Polyester Knitted fabric Inspection knowledge to excel in this role. As a Quality Assurance Manager, your responsibilities will include: - Developing, managing, implementing, communicating, and maintaining a quality plan to ensure compliance with quality system requirements - Monitoring quality using a 4 point system - Leading the fabric QA/Inspection team and providing technical guidance - Collaborating with Knitting fabric & Dyeing factories to establish the best quality system and holding them accountable to standards and KPIs - Anticipating fabric quality issues and providing solutions - Coordinating with various departments such as Knitting, Dyeing, Finishing, Merchandis...

As an experienced HR professional with over 5 years of experience and an MBA in HR, you will be responsible for various key aspects within the HR department, ensuring the recruitment process and overall quality system are effectively managed. Your role will involve the following key responsibilities: - Understanding and executing staffing requisitions, requirements, and issues from all departments. - Drafting and updating various HR-related documents such as job descriptions, employee handbook, performance appraisal forms, SOPs, and policies. - Sourcing candidates through recruitment agencies and online job advertisements. - Screening candidates through resume shortlisting, phone interviews,...

As a Production Head with 15 to 19 years of experience in pharma API pharma at Sandhurst Road Mumbai, your responsibilities include: - Reviewing, approving, and distributing work instructions for manufacturing activities. - Carrying out production activities as per the production plan. - Deciding on new batch production and monitoring batch processes. - Qualification of production equipment and participation in validation activities. - Checking the quality system in the production department. - Preparing equipment master lists and equipment qualification plans. - Reviewing MFRs, BMRs, BPRs, SOPs, and formats. - Ensuring that all production deviations are reported, evaluated, and investigated...

Role Overview: As an Assistant Manager - Quality Assurance in Chemistry, your role will involve managing and controlling various aspects of quality management and continuous improvement in the API industry. You will be responsible for implementing and maintaining quality systems at the site, conducting investigations, reviewing documentation, ensuring compliance with regulatory requirements, and coordinating various activities within the organization. Key Responsibilities: - Management and control of SOPs, Master documents, labels & other GMP impacted documents - Implementing necessary quality systems including complaint investigation, qualification and validation, change control, deviation ...

As a candidate for this role, you will be responsible for maintaining the Laboratory's Quality System, performing analytical tests in the laboratory, assisting with laboratory administrative duties, maintaining smooth laboratory workflow, obtaining lab certifications, completing QA/QC assignments, and promoting good customer relations. Qualifications required for this position include: - B.Sc in Chemistry (full time) from reputed Institutions with consistently good academic record. - Experience of working at Ports handling oil/gas/petroleum products will be an added advantage.,

As a Leadership & Development Manager at Teva Pharmaceuticals TAPI, your role involves evaluating training needs and delivering training materials for Manufacturing, Quality, and Support groups. You will ensure compliance with training policies and procedures, administer the Learning Management System (LMS), and coordinate training activities. Your responsibilities include: - Developing curricula for on-the-job training requirements - Maintaining a compliant training record-keeping system - Preparing training completion metrics for Quality Review Board meetings - Determining training frequency/re-training intervals based on roles and responsibilities - Assisting in developing training assess...

Responsible for setting up standards for Incoming, In-process, and finished goods quality, checking, whether quality standards are in line with global standards, securing relevant quality certifications (IMS) Integrated Management System for the company. Quality system / IMS establishment planning and follow up the progress. Preparation of documentation in line with QMS requirements. Ensuring that the ISO: 9001: 2008. Preparing a list of internal auditors for QMS/process/product as per the requirement and getting them trained and certified by Concerned agencies Specific knowledge of quality management systems, e.g., ISO 9001,IATF16949, TQM

You will be responsible for supervising the work of department technicians and ensuring effective implementation of the Quality System. Your key responsibilities will include: - Preparing Test Procedures as necessary - Ensuring the quality of test results generated - Updating all documents and records in your department - Providing in-house training to subordinates as required - Periodically assessing subordinates on quality consciousness, quantity of work performed, discipline, and overall behavior/attitude and suggesting training needs - Maintaining confidentiality of information regarding patients No additional details of the company are mentioned in the job description.,

As an Associate R&D (DQA) at our company in Jhagadia, you will be responsible for the following key responsibilities: - Review Lab Validation Protocols/Reports (CRD) and Method Development/Validation documents (ADL). - Review specifications and STPs for raw materials, intermediates, and finished products. - Support DMF filings, stability studies, and regulatory documentation. - Prepare/review SOPs, logbooks, and ensure RA & GLP compliance. - Collaborate with R&D, QA, ARD, and Regulatory Affairs teams. - Support internal and external audits (FDA, ISO). - Handle DQ, IQ, OQ, and PQ documentation for equipment. - Maintain adherence to cGMP and regulatory standards. Qualifications required for th...

As a Lead Auditor for Multiple Management System Certification in Cotecna, your role involves actively ensuring CQR compliance in terms of Quality and Integrity of the certification process. Your mission includes achieving and maintaining accreditation and Scheme approval for all certification Services/Product Schemes. To support the Certification business, you will be responsible for developing a strong back office and a competent/knowledgeable Audit team for the independent and impartial execution of audit activities. Key Responsibilities: - Administer procedures related to Certification Services/Product schemes - Achieve and maintain accreditation and Scheme approval for all certification...

As an AGM/DGM-Manufacturing at the leading High speed sheet metal stamping industry in Bangalore, your role will involve the following key responsibilities: - Leading the team of PPC, Production, Quality, Tooling and Maintenance - Ensuring 100% On-Time Delivery (OTD) - Monitoring machine capacity and planning for capacity expansion based on sales projection - Managing inventory and monitoring Raw Material (RM) & Work-in-Progress (WIP) levels - Minimizing the breakdown of critical machineries through regular and timely preventive maintenance Qualification Required: - BE/PG in Mechanical/Production Engineering Experience: - 15-20 Years Salary Offer: - Up to 35 LPA Functional Skills Required: -...

As a Drilling Solutions Engineer at NOV Reedhycalog in Mumbai, India, your role will involve identifying new opportunities, expanding product development, and maximizing profitability for customer accounts. You will be responsible for various key areas: **Key Responsibilities:** - **Customer Service:** - Maintain good relationships with customer accounts personnel and attend to their requirements efficiently. - Deliver technology presentations and training sessions when necessary. - Monitor customer issues, feedback, deadlines, and deliverables to ensure effective handling of customer issues. - Ensure timely, complete, and accurate invoicing according to NOV and local customer legal requirem...

Job Description Job title: Regulatory Affairs Operations Specialist Your role: Assisting, supporting, coordinating and preparing regulatory submissions for product licensing to ensure accuracy and expedite approval processes and identifies, defines and addresses problems that are not immediately evident but typically not complex. The role works under general supervision, exercises independent judgment within established processes and fosters productive internal and external relationships to resolve mutual problems and contribute to streamlined operations. The role performs Change Management activities including hosting meetings to acquire change details for sustaining products, notifying geo...

1.Establishment, Implementation and Maintenance of Quality system. 2.Approval of Standard Operating Procedures, Master Batch Manufacturing and Master Batch Packing Records. 3. Authorization of written procedures and other documents including amendments like Master Formula Records, Raw Material specifications, Packing Material specifications, Product specifications & General Analytical Specifications. 4. Monitoring of Compliance with GMP requirements. 5. Review and approval of change control, deviations, Risk assessment, Corrective action Preventive actions and other Quality management system related documents. 6. Inspection, investigation and taking of samples in order to monitor factor that...

fabrication & rubber mfg. working only Strong knowledge ISO 9001 & 14001, ISO 45001, SPC, FMEA, control plans, Navision systems, digital quality dash, Quality Systems & Compliance, Process QC, Leadership, Customer & Supplier Interface, Lab & Testing

Role Overview: You will be responsible for coordinating the Integrated Management System (IMS) at different documentation levels. This includes internal audits for Systems, Process, and Product to ensure compliance with the IMS through the Annual IMS Program. You will also coordinate Cross Audits (PO), measure the performance of the Quality System, and coordinate surveys requested by clients. Additionally, you will be a member of multidisciplinary teams for continuous improvement. Key Responsibilities: - Coordinate the IMS at different documentation levels - Coordinate internal audits (Systems, Process, and Product) to ensure IMS compliance - Coordinate Cross Audits (PO) - Measure the perfor...

Role Overview: You will be responsible for ensuring the optimal functionality, safety, and technical readiness of simulators. This role involves a combination of hands-on preventive and corrective maintenance tasks, as well as providing technical assistance and support. Your objective will be to maintain high availability and performance of the simulators while offering engineering insights and operational guidance to the maintenance team. Key Responsibilities: - Perform scheduled preventive maintenance on simulators according to established procedures and schedules. - Identify and resolve technical and mechanical issues in simulators effectively. - Coordinate with departments for inspection...

Position - Deputy Manager- Mechanical Employment Type- Fixed Term Employment on ERDA Rolls for 03 Years, it will be regularised, based on performance. Location- Makarpura, Vadodara Qualification- Essential: BE/ ME / M.Tech (Mechanical Engineering) Experience Description- (Minimum 12 years to Maximum 18 years) Work experience in a testing laboratory or quality control department of industries in field of Mechanical testing Key Responsibilities 1. To plan and monitor the day-to-day activities of mechanical section (including HTLS lab and Seismic lab) 2. To achieve the revenue targets of section 3. To prepare capital & recurring expenditure budget for the section and take suitable actions/measu...

As a Drilling Solutions Engineer at NOV Reedhycalog in Mumbai, India, your role will involve customer-facing engineering tasks such as identifying new opportunities, expanding product development, and maximizing profitability for accounts. You will be responsible for maintaining good relationships with customer accounts personnel, delivering technology presentations and training sessions, and monitoring customer issues and feedback to ensure effective handling. Additionally, you will support sales by qualifying opportunities, creating technical evaluations, and reviewing customer orders. Your reporting duties will include creating application maps, maintaining product offering maps, capturin...

As a part of this role, you will be involved in the development of new projects and application program testing on gluing robots. Your responsibilities will include monitoring the quality of glued parts and evaluating applicator efficiency. You will also be tasked with the development and control of Level 0 and Level 1 maintenance for equipment in MP9, such as robots, purge systems, primer, and glue. Ensuring compliance with quality system requirements and developing best practices for the gluing cell will be key aspects of your role. You will be expected to create operational practices and procedures (PPCM), control application flows and patterns, and develop templates to evaluate the adhes...

Role & responsibilities To ensure consistent product quality in SMT manufacturing processes by implementing quality Ensure timely reporting of non-conformities (NC) or deviations from specifications. systems, conducting inspections and lab tests, analyzing defects, and driving process improvements in line with customer and regulatory requirements. Check and test products to make sure they meet quality standards. Work with the production and engineering teams to fix any issues. Find Investigate product non-conformities and process deviations using 5 Why, Ishikawa, Fishbone, and Pareto analysis. Prepare and maintain Control Plans, PFMEA, PPAP, as per IATF 16949 / ISO 9001. Conduct quality insp...

As the Production Head, you will be responsible for overseeing the manufacturing activities in the pharma API industry. With 15 to 19 years of experience, you will be based at the Sandhurst Road Mumbai head office with a salary of 15 lpa. Your key responsibilities will include reviewing, approving, and distributing work instructions for manufacturing activities. You will ensure the production activities align with the production plan and make decisions regarding new batch production. Monitoring batch processes and reviewing online documentation such as BMR, BPRs, logbooks, and daily records will also be part of your role. Furthermore, you will be in charge of qualifying production equipment,...

You should hold a B.Sc in Chemistry from a reputed institution with a consistently good academic record. Experience in working at ports handling oil, gas, or petroleum products would be beneficial for this role. Your main responsibilities will include maintaining the laboratory's Quality System, conducting analytical tests, assisting with administrative tasks, ensuring smooth workflow in the laboratory, obtaining lab certifications, completing QA/QC assignments, and fostering positive customer relations. Additionally, you may be required to perform other duties as assigned.,

As an Associate R&D (DQA) at our company located in Jhagadia, you will play a crucial role in the Research & Development department. You are required to have a qualification of M.Sc. in Chemistry or a related science field along with a minimum of 4 years of experience, preferably in the pharmaceutical industry. Your primary responsibilities will include reviewing Lab Validation Protocols/Reports (CRD) and Method Development/Validation documents (ADL), as well as reviewing specifications and STPs for raw materials, intermediates, and finished products. Additionally, you will be supporting DMF filings, stability studies, and regulatory documentation, preparing/reviewing SOPs, logbooks, and ens...