Senior Specialist Quality control

Posté 10 nov. 2022

Bangalore, Karnataka - India

Demander un identifiant 257303

 

A career at our company is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.

 


  • Completion of sampling and analysis on time as per turnaround time.
  • Compliance to KPI and ensure first time right analysis.
  • Involve in CAPEX preparation, Quotation and URS requirements of QC
  • Perform the sampling for the Raw material and finished product.
  • Contribute to method development and improvements, analytical method verification, cleaning verification and process verification.
  • Analysis of samples for retest/shelf life as per timelines and providing data.
  • Perform the root cause analysis activity.
  • Completion of analysis, uploading of data in SAP and release or rejection of batches.
  • Completion of the oligo QC analysis and verification and release of batches in CPP.
  • Preparation of Certificate of analysis
  • Participate actively in trainings
  • Maintenance of logbooks, registers, and documents in QC online
  • Maintains all analytical equipment/instruments in QC
  • Calibrates analytical / test equipment as necessary.
  • Maintains a neat and orderly workplace and office.
  • Stocks supplies, verifies inventories and orders fresh stocks for key reagents and salts as required.
  • Prepares necessary standards and stock solutions as necessary
  • Write and revise SOP’s before due date.
  • Documents results and observations per department guidelines (e.g., Lab Notebook, Project Files)
  • Communicates technical results to supervisors, customers, and colleagues.
  • Monitor all parameters as required in a shift and records all observations during shift
  • Understand and follow process & procedures laid down in Quality management system (QMS).
  • Ensure compliance to QMS
  • SOP preparation, Quality Audits, Complaint Management & documentation management
  • Responsible for execution of a wide range of analytical methods, quality assurance and control tests to suit a wide range of chemicals produced/used at various stages of production and research in a contract research and custom synthesis lab.
  • Document all analytical data in electronic format.
  • Involvement in investigations to identify the reasons for any defect in quality.
  • Implement Kaizens to cut costs, reduce safety hazards, raise purity, or suggest changes to improve batch-to-batch consistency.


What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology. We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring their curiosity to life!
 

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