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3 Quality Policies Jobs

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4.0 - 15.0 years

0 Lacs

erode, tamil nadu

On-site

The Quality Assurance Manager - Woven will require a minimum of a B.Tech / BE or Diploma in Textile or a relevant degree along with 4 to 15 years of experience in the field. Your role will involve having a deep understanding of garment construction, particularly shirts, fabric properties, and quality standards in stitching, finishing, and overall appearance. You should be proficient in quality control techniques such as AQL standards and be able to identify defects, root causes, and implement corrective actions. Setting quality standards based on buyer requirements, providing guidance to departments and processes, and establishing SOPs for production and preparatory processes to ensure right-first-time quality are crucial aspects of your responsibilities. Developing management information systems for quality measurement and recording, ensuring compliance with established quality standards, monitoring product quality throughout production stages, and training new quality personnel on company quality policies and tools are key components of the role. Woven experience is a must for this position. This is a full-time, permanent role with benefits including Provident Fund. The work location is on-site.,

Posted 3 days ago

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10.0 - 14.0 years

0 Lacs

vadodara, gujarat

On-site

As Manager 2 in the Corporate Quality department at SUN Pharma, you will be responsible for overseeing the quality aspects of contract manufacturing organizations (CMOs) involved in manufacturing site transfer products for the US market. Your primary focus will be to ensure compliance with SUN Pharma Quality and Compliance Standards as well as global regulatory requirements. Your essential job functions will include monitoring and overseeing activities at CMO sites to ensure adherence to SUN Pharma standards and regulatory guidance. You will conduct regular oversight visits, prepare visit reports, and serve as the main point of contact for coordination between SUN site, commercial team, corporate quality audit, and CMO site on manufacturing and technical matters. Additionally, you will be involved in authoring and reviewing quality agreements, ensuring the use of qualified service providers, participating in process validation batches, reviewing quality system documents, conducting visits based on market complaints/recalls/CAPA, reviewing batch records, stability data, and analytical reports, as well as preparing and reviewing SOPs. Your role will also include participation in the initial evaluation of CMOs, supporting regulatory audits at CMO sites, engaging in critical investigations, initiating QMS documents, preparing for regulatory agency inspections, participating in product release site audits, maintaining audit-related documents, preparing monthly reports, staying updated on regulations through training, and following Corporate Quality Policies/Global Quality Standards and Regulatory Guidelines. To be successful in this role, you should have an M.Sc./B.Pharm/M.Pharm or equivalent degree along with a total of 10 years of industrial experience and knowledge. You will also be expected to participate in and execute project work assigned by your reporting authority. If you are looking for a challenging opportunity to ensure quality compliance in contract manufacturing organizations and contribute to the overall quality standards of SUN Pharma, this role is ideal for you. Join us in our mission to maintain high-quality standards and regulatory compliance in the pharmaceutical industry.,

Posted 6 days ago

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8.0 - 12.0 years

0 Lacs

chennai, tamil nadu

On-site

You will be responsible for supporting the objectives of the Health, Safety, Security, Environmental, Sustainability, and Quality Policies as well as the Information Security Management Policy by adhering to applicable Procedures and Work Practices while fulfilling your duties. Your role will involve carrying out various piping activities, preparing deliverables as identified in Functional Competencies, and signing drawing/documents as an originator in accordance with correct procedures. Ensuring quality in design, technical accuracy in the preparation of drawings, material quantities, etc., will be a key part of your responsibilities. You will execute assigned work in accordance with applicable contract procedures, client, and project standards. Adhering to engineering procedures for design safety and adopting safe attitudes towards engineering design, as well as raising features affecting the safety and integrity of the project with appropriate authorities, will also be expected. You will be responsible for the correct implementation of all piping CAD and system-related functions for your appointed area. To be successful in this role, you should have a minimum of 8 years of experience in the detail engineering of process plants. Project/site experience working in a variety of projects including grassroots, brownfield, and revamp types is essential. You should possess sound knowledge of all general piping design, developing experience in piping layout, and phases of plot plan development. Some experience in site-based design in support of construction is preferred. Being experienced and proficient in executing work using intelligent CAD systems will be advantageous. Wood is a global leader in consulting and engineering, helping to unlock solutions to critical challenges in energy and materials markets. They provide consulting, projects, and operations solutions in 60 countries, employing around 35,000 people. Learn more about Wood at www.woodplc.com.,

Posted 2 weeks ago

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