Process Engineer

2 - 6 years

0 Lacs

Posted:21 hours ago| Platform: Shine logo

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Work Mode

On-site

Job Type

Full Time

Job Description

You are passionate about improving healthcare through fast, accurate diagnostic testing at Cepheid. Your mission drives you every moment of every day as you contribute to scalable solutions addressing the world's most complex health challenges. You are involved in all stages of molecular diagnostics, from ideation to the development and delivery of testing advancements that enhance patient outcomes across various settings. As a valued member of the team, you can have an immediate, measurable impact on a global scale in an environment that nurtures career growth and development. Cepheid collaborates with six fellow Danaher Diagnostics companies, collectively working at the forefront of change to develop diagnostic tools that tackle significant health challenges. You play a crucial role as a Process Engineer, responsible for formulating and executing strategies to achieve continuous process performance improvements concerning Safety, Quality, Delivery, and Cost of a manufacturing process or line. Your involvement in continuous improvement initiatives includes overseeing overall equipment/process performance, executing equipment/process validations, tracking efficiency, and problem-solving. Leveraging your process knowledge, you identify opportunities and solutions to enhance throughput capacity by mitigating constraints" impact. You will closely interact with global teams and serve as the technical partner to the engineering/manufacturing teams in the US, Sweden, and India throughout the equipment/process life cycle. Based in Cepheid's MII Bangalore Plant at Mahadeva Kodigehalli, Bangalore, you will have the opportunity to: - Lead the definition and execution of installation and validation processes for new or existing equipment and products in adherence to company standards, IVD regulations, and GMP standards. - Plan and execute documentation following QMS requirements, including the preparation, writing, and filing of validation plans, SOPs, protocols, and reports. - Utilize relevant continuous improvement tools to enhance production uptime, reduce unplanned maintenance, minimize WIP or plant inventories, and implement cost reduction initiatives across equipment and labor. The essential qualifications/requirements for this role are: - A Bachelor's or Master's degree in biotechnology or related engineering fields with a minimum of 2 years of manufacturing experience, preferably in the Medical Device/IVD sectors. - Proficiency in equipment and product validation for medical device manufacturing, with an understanding of mechanical design concepts and machinery such as mixing processes, motors, pumps, vacuum, and hydraulics. - Experience in a regulated work environment (ISO, GMP, Medical Device regulations). Join the winning team at Cepheid today and together, accelerate the real-life impact of tomorrow's science and technology. Collaborate with customers worldwide to address their most complex challenges and design solutions that bring the power of science to life. For more information, visit www.danaher.com.,

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