Description: This role is responsible for conducting in-process and final product quality testing and analyses in strict compliance with established standards and regulatory requirements within a global pharmaceutical manufacturing environment. The incumbent interprets and evaluates analytical results
Description: This role is responsible for conducting in-process and final product quality testing and analyses in strict compliance with established standards and regulatory requirements within a global pharmaceutical manufacturing environment. The incumbent interprets and evaluates analytical results
Description: The position is responsible for in-process and final product quality analyses and inspection in compliance with approved standards and regulatory requirements. The role involves interpreting and evaluating analytical results for accuracy and precision against established
Install, maintain, and repair internal factory equipment. Supervise employees who perform maintenance and tool making. Responsible for departmental operations planning/execution or is focused on execution of professional activities within a technical discipline. Functions with some autonomy
Drive and coordinate Quality Control activities for Incoming Inspection are to ensure zero shop complaints and to improve in overall inspection processes. Your Role: Knowledge about basic EHS guidelines/Environmental aspect and Risk related to inspection activities
As a Turbine Lead Project Engineer, you will lead the mechanical scope of one or several nuclear steam turbine projects. You will be part of a project team and coordinate engineering activities within the design office,
Our vision is to transform how the world uses information to enrich life for all. Micron Technology is a world leader in innovating memory and storage solutions that accelerate the transformation of information into intelligence, inspiring
Qualification: M. Sc/B. Pharma. Experience: Analyst in physical activity like Handling of UV visible spectrophotometer, Karl Fischer, Water content determination, Particle Size determination, Titration. and having knowledge of LIMS. Having knowledge about cGMP and good laboratory practices.
Review analytical data for Raw Materials (RM), Packaging Materials (PM), in-process samples, Finished Products (FP), stability samples, working standards, reference standards, and other test samples. Review and approve Certificates of Analysis (COAs) for RM, PM, in-process
Description: The role provides independent and objective assurance and advisory support to enhance organizational effectiveness and risk mitigation. The role evaluates the reliability and effectiveness of risk management, governance, and internal control processes across financial, operational,
Responsible to perform and monitoring all the activities related to Aseptic area. Responsible to perform the cleaning and sanitization of machines, instruments and equipment’s and area. Responsible for line clearance activity before commencing the operations. Responsible
At ABB, we help industries run leaner and cleaner—and every person here makes that happen. You’ll be empowered to lead, supported to grow, and proud of the impact we create together. Join us and help run
Company Overview Nikkiso Clean Energy & Industrial Gases is a leading provider of cryogenic pumps, heat exchangers, process systems, turboexpanders, services, and solutions for the liquefied natural gas (LNG), liquefied hydrogen (LH2), and industrial gases industries.
Description: This role is responsible for creating, reviewing, and maintaining technical documentation related to quality control processes and activities in compliance with established standards and regulatory requirements within a global pharmaceutical manufacturing environment. The incumbent ensures
An Introduction to Codal Codal is an award-winning web design and development consultancy that helps enterprise organizations solve complex problems and accelerate growth through elegant, data-driven digital solutions. Our areas of expertise include application modernization, eCommerce,
Description: This role is responsible for leading and managing quality control operations within a pharmaceutical manufacturing environment, ensuring compliance with established standards and regulatory requirements. The incumbent oversees in-process and final product quality analyses and inspections,
Description: Operate and monitor manufacturing equipment and Instrument used in various stages of API production, such as reactors, Centrifuge, Dryer, Miller, sifter etc. Maintaining accurate records and documentation of production activities, including batch Manufacturing Record (BMR),
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 unknown
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: 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