Job Responsibility: ❖ To prepare validation documents such as Installation qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) and other qualification documents for equipment /utilities/facilities. ❖ To initiate change control and other documents in Caliber QAMS and
Key Responsibilities: Responsible for review of URS, DQ and vendor/ supplier’s documents related to qualification. Responsible for preparation and review of Validation/ Qualification protocol and report. Responsible for execution and review of Qualification / Re-Qualification and Validation activity
Job Title: Design Documentation & Validation - Senior Executive. Department: Endoscopy and Women Healthcare Location: Vapi, Gujarat Reports To: Manager / Senior Manager – Endoscopy and Women Healthcare Job Purpose: To prepare, maintain, and manage design documentation
Job Description Role: Senior Quant Developer – AI Location: Remote / Kraków / Ho Chi Minh City / Ahmedabad Employment Type: Full-Time Experience: 5+ Years About Client They are building an AI-driven trading and investing platform
Actylis is a global solutions provider with over 75 years of experience, specializing in streamlining the management of critical ingredients and raw materials for our business partners. We offer both sourcing and manufacturing solutions tailored to
Actylis is a global solutions provider with over 75 years of experience, specializing in streamlining the management of critical ingredients and raw materials for our business partners. We offer both sourcing and manufacturing solutions tailored to
The Stator Lead Design Engineer will design generators, realize manufacturing and contractual documentation. He/She participates to improvement actions and manage the sub-contracted studies. He/She supports the other teams (Methods, Manufacturing, Sourcing) for all topics related to
Req ID:515416 At Alstom, we understand transport networks and what moves people. From high-speed trains, metros, monorails, and trams, to turnkey systems, services, infrastructure, signalling and digital mobility, we offer our diverse customers the broadest portfolio
Description: The role is responsible for ensuring real-time compliance with global GMP (Good Manufacturing Practices) across manufacturing, packing, and dispensing operations. The role provides on-floor quality oversight, ensuring that all activities are executed as per approved
Description: To Prepare new SOPs as per required, revise existing SOPs based on periodic updation and as per internal & external audit recommendation after that review and implemented SOPs of Production department. To Carryout process validation and
About Business: Adani Group: Adani Group is a diversified organisation in India comprising 10 publicly traded companies. It has created a world class logistics and utility infrastructure portfolio that has a pan-India presence. Adani Group is
Extractables & Leachables (E&L) Execute extractables and leachables studies for pharmaceutical packaging materials, process contact materials, and device components. Perform sample preparation, extraction studies, and analytical testing as per study protocols. Support identification and characterization of
Description: Analytical Development - Injectable & Complex Injectable This role supports the development of drug substances and drug products by contributing to the design and execution of analytical methods used to evaluate quality attributes across various
Description: Analytical Development - Injectable / Complex Injectable The position supports peptide and oligonucleotide drug substance (DS) and drug product (DP) development through the development, optimization, validation, transfer, and application of advanced analytical methods to evaluate critical
Description: This role supports the development of drug substances and drug products by contributing to the design and execution of analytical methods used to evaluate quality attributes across various dosage forms, with a specific focus on
Lingénieur Lead Design Stator conçoit des alternateurs, réalise la documentation pour la fabrication et la documentation contractuelle. Il/Elle participe aux actions d’améliorations et gére les études sous-traitées. Il/Elle supporte les autres équipes (méthodes, Usine, Sourcing) pour
About the Company e.l.f. Beauty, Inc. stands with every eye, lip, face and paw. Our deep commitment to clean, cruelty free beauty at an incredible value has fueled the success of our flagship brand e.l.f. Cosmetics
Company Description At AECOM, we’re delivering a better world. We believe infrastructure creates opportunity for everyone. Whether it’s improving your commute, keeping the lights on, providing access to clean water or transforming skylines, our work helps
Description: 1. Execution of multi-step synthesis of projects which are transferred or developed in R&D lab. 2. Depending on the project requirements, performing lab experiments to gather process understanding. 3. Monitoring validation batches in R&D lab as
Description: The role supports engineering operations across the organization with responsibility for utility systems used in pharmaceutical manufacturing. The role ensures quality, safety, reliability, cost, timeliness, and performance standards are met through effective operation, monitoring, testing,