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4.0 - 8.0 years
0 Lacs
surendranagar, gujarat
On-site
As a Sr. Executive / Assistant Manager Quality Assurance (QA) at SAVA Healthcare Limited, Surendranagar Plant, your primary responsibility is to ensure the implementation and maintenance of cGMP practices, quality systems, and compliance with regulatory requirements. You will oversee QA activities including documentation, validations, audits, and shop floor compliance to uphold product quality and regulatory adherence. Your key responsibilities will include ensuring compliance with cGMP, SOPs, and regulatory requirements on the manufacturing floor, reviewing and approving batch manufacturing records (BMRs) and batch packing records (BPRs), handling deviations, change controls, CAPA, and qual...
Posted 2 months ago
10.0 - 15.0 years
0 Lacs
andhra pradesh
On-site
As the Manager Quality in the Spinning Unit located in Edlapadu, your primary responsibility will be to oversee and lead the quality function of a large spinning unit with 100,000 spindles. Your role will be crucial in ensuring the consistent delivery of high-quality yarn for both local and export markets while focusing on achieving superior yarn quality, addressing customer feedback, and upholding compliance with social and sustainability standards. Your key responsibilities will include ensuring adherence to specified quality parameters for various types of yarn such as combed warp, hosiery counts, dyed packages, core-spandex, slub yarns, and export-grade yarns. You will be required to mon...
Posted 2 months ago
5.0 - 9.0 years
0 Lacs
maharashtra
On-site
As a Validation Specialist at Piramal Pharma Solutions, your primary responsibility will involve preparing and updating various validation documents to ensure compliance with regulatory requirements. This includes developing Validation Master Plans (VMP), Process Validation protocols, Computer System Validation protocols, and reports. You will also be responsible for creating product matrices, Cleaning Validation/Verification protocols, qualification/requalification protocols for equipment/instruments, utilities, and facilities, as well as area validation protocols and reports. In addition to validation activities, you will be involved in quality risk assessments, review of calibration certi...
Posted 2 months ago
5.0 - 9.0 years
0 Lacs
pune, maharashtra
On-site
You are dedicated to enhancing daily living through innovative, ergonomic solutions that promote comfort and well-being. Your mission is to design the next generation of products to empower people to walk, sit, and sleep better. Each product you create is fueled by the same passion that drove you to innovate from day one: to give people the freedom to do more. Join the mission to transform everyday struggles into freedom and joy. Discover Frido and experience the freedom to live life your way. You are seeking a skilled and experienced Production Engineer to oversee the manufacturing process of polyurethane memory foam products. The ideal candidate will have a deep understanding of polyuretha...
Posted 3 months ago
6.0 - 10.0 years
0 Lacs
jharkhand
On-site
Job Description: As a member of the team, you will be responsible for identifying, reviewing, and implementing Pharmacopeial updates on a global scale. This will involve conducting activities related to the revision of product specifications and methods through a change management process. You will also be required to assess the impact of changes and review updates to ISO Guidelines. Additionally, you will collaborate with various departments to ensure compliance with USP/NF or other Pharmacopeial standards and ISO Guidelines. Regular reporting of work completion status to the reporting manager and coordination with them for updates to the management will be essential tasks. You will also be...
Posted 3 months ago
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