Cepheid Process Engineer Job
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Cepheid Process Engineer Job For MSc Biotech, Biochem – Apply Online

Cepheid Process Engineer Job For MSc Biotech, Biochem – Apply Online. Cepheid Life Sciences companies jobs. Bengaluru engineer vacancies. Process Engineer Jobs Bangalore. Karnataka biotechnology Jobs. Check out all of the details on pall corporation jobs below

Name of the Post – Process Engineer


  • Bengaluru, Karnataka, India
  • Orag, Tamil Nadu, India

Job ID – R1216012

The Process Engineer is responsible for developing a strategy and executing a plan to deliver continuous process performance improvements related to the Safety, Quality, Delivery, and Cost of a manufacturing process or line. The Process Engineer will work with continuous improvement initiatives and be responsible for overall equipment performance and executing equipment validations, including efficiency tracking and problem-solving. The Process Engineer will also leverage process knowledge to identify opportunities/solutions to improve throughput capacity by reducing the impact of constraints.

The role will require close interaction with the global “Make in India” project team as this is a greenfield project with the aim of establishing local manufacturing in India with most equipment being built and shipped from the US. This person will be the technical partner to the engineering/ manufacturing team in USA/ Sweden

/ India throughout the life cycle of the equipment.

This position is part of  Cepheid’s MII Bangalore Plant and will be located in Mahadeva Kodigehalli, Bangalore.

In this role, you will have the opportunity to:

  • Be the primary lead for defining and executing installation and validation processes for new or existing equipment and products in compliance with company standards, IVD regulations and GMP standards
  • Plan & execute documentation as per QMS requirements, including preparation, writing and filing of validation plans, SOPs, protocols and reports
  • Apply knowledge of relevant continuous improvement tools and approaches to increase production up-time, minimize unplanned maintenance, minimize work in process inventories (WIP) or plant inventories, and implement cost reduction initiatives across equipment and labour
  • Effectively interface and partner with other engineering disciplines, such as Controls & Automation engineering and with the Manufacturing team.
  • Plan, compile and evaluate test data to determine appropriate limits and variables for process or material specifications. Responsible for driving assemblers’ engagement and for developing Lean and Six Sigma capabilities through coaching and mentoring.

The essential requirements of the job include:

  • Bachelors/Masters in Biotechnology/Biochemistry or related engineering fields
  • Minimum 2 years of experience in manufacturing, preferably in medical device/IVD sectors
  • Strong background in equipment and product validation for medical device manufacturing. Understanding of mechanical design concepts and machinery: mixing processes, motors, pumps, vacuum, and hydraulics
  • Experience working in a regulated work environment (ISO, GMP, Medical Device regulations)
  • Proven experience in leading and delivering improved results to set targets and timelines.

It would be a plus if you also possess previous experience in:

  • Working in a global environment. Strong communication, written and oral presentation skills (English)
  • Strong analytical and problem-solving skills combined with a strong technical understanding. Experience with Lean manufacturing and Six Sigma
  • Flexibility to work off-shifts and weekends if required at call-in


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