Role Summary: An Equipment Maintenance Engineer is responsible for ensuring the optimal performance, reliability, and safety of machinery and equipment used in pharmaceutical industry. This role involves planning and executing preventive and corrective maintenance, troubleshooting equipment
Role Summary The Applied System Engineer is responsible for the engineering design and technical execution of equipment packages within the Site Order Engineering team. The role ensures that assigned order engineering activities are completed in accordance
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Career CategoryInformation Systems Job Description Position Summary Amgens Drug Substance Technologies - Synthetics (DSTS) organization within Process Development (PD) is responsible for the invention, development, and implementation of drug substance manufacturing processes and technologies that advance
MISSION STATEMENT Main Job Purpose: The RA/QA Operations Specialist supports the Responsible Person (FvP) in ensuring full compliance with Swissmedic, GMP and GDP requirements for all regulated activities related to import, distribution, release and lifecycle management
Security Strategy Contribute to business Security strategy and Security roadmap by providing site perspective as per Site Security Plan. Align the site security strategy with the group policy Lead strategic initiatives aligned to business requirements at
Requisition ID: 293547 Relocation Authorized: None Telework Type: Full-Time Office/Project Work Location: Vadodara, Chennai, Gurugram Competencies Overall Interview Rating Extraordinary teams building inspiring projects: Since 1898, we have helped customers complete more than 25,000 projects in
Vodafone Idea Limited is an Aditya Birla Group and Vodafone Group partnership. It is India’s leading telecom service provider. The Company provides pan India Voice and Data services across 2G, 3G and 4G platform. With the
Essential Functions Perform microbiological testing of APIs, purified water, and environmental samples as per approved specifications and methods. Conduct sampling and testing of water systems (PW) and environmental monitoring (air, surface, personnel) in classified areas. Carry
Be the First to Apply DivisionPiramal Critical Care Piramal Critical Care (PCC), a business unit of Piramal Pharma, is the fourth-largest producer of inhaled anesthetics and a global player in hospital generics. We are motivated by
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: Ther role is accountable for leading the design, development, implementation, and optimization of pharmaceutical manufacturing processes to ensure efficient, economical, scalable, and compliant mass production. The role provides strategic direction across process design, equipment layout,
Make an impact with NTT DATA Join a company that is pushing the boundaries of what is possible. We are renowned for our technical excellence and leading innovations, and for making a difference to our clients
Job Description Preparation & Review of SOP’s of QA system and review / approval of SOP’s of other departments. Review of master BMR/BPR of commercial and exhibit batches. Review of BMR / BPR, scale-up and placebo
Req ID:525197 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
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
Description: Managing overall activity of QMS. Establishing and implementing quality systems to comply cGMP. Handling of Product Complaint, Deviation, OOS (Out of Specification), OOT (Out of Trend), Incident and Change Control. CAPA management, tracking, verification of implemented
Job Family:GIC Process (India) Travel Required:None Clearance Required:None What You Will Do: Perform end-to-end Quality Assurance (QA) on AML investigations reviews across Retail Banking and Crypto domains Assess analyst decisions on customer risk profiling, transaction analysis, sanctions
Description: This role is responsible for conducting in-process and final product quality analyses and inspections in strict compliance with established standards and regulatory requirements within a global pharmaceutical manufacturing environment. The incumbent interprets and evaluates analytical
Description: Manage User Access Management (UAM) activities for Production Shop Floor GxP applications, including user provisioning, modification, deactivation, periodic access reviews, and compliance with regulatory requirements. Handle IT-related QMS activities such as Deviation, CAPA, Change Control, Incident