Quality Analyst Jobs at Merck | Chemistry, Chemical Engineering Graduates Apply Now 

Quality Analyst Jobs at Merck | Chemistry, Chemical Engineering Graduates Apply Now 

Are you looking for Quality Analyst Jobs in Bangalore with a global science leader? This Analyst – Quality Services role is part of Merck careers, offering exciting opportunities for professionals from BSc Chemistry Jobs and Chemical Engineering Jobs backgrounds. The role focuses on analytical quality services, QC testing, and compliance within healthcare, life science, and electronics domains.

About Merck

Merck is a global science and technology leader operating across Healthcare, Life Science, and Electronics, delivering innovative solutions that improve lives worldwide. Through Merck careers, the company offers rewarding opportunities in Quality Analyst Jobs, Analyst – Quality Services roles, and laboratory-based scientific careers. With strong quality systems aligned to ISO standards, Merck supports professionals from BSc Chemistry Jobs and Chemical Engineering Jobs backgrounds to grow through continuous learning and innovation. The organization values diversity, inclusion, and scientific excellence, creating a collaborative work environment for individuals passionate about quality, analytics, and technology-driven progress.

Details

  • Job Title: Analyst – Quality Services
  • Job ID: 294388
  • Location: Bangalore, Karnataka, India

Responsibilities

  • Work with team members and collaborate across departments on assigned projects.
  • Cost-effective management of entrusted resources.
  • Support Operations and Quality Programs.
  • Generate
    QC data and a certificate of analysis for certified reference materials.
  • Support Quality Control Release Testing of items manufactured at the MilliporeSigma-RTC site and other assigned projects.
  • Work closely with senior team members on multiple aspects, including data analysis, documentation, and data review, to support the release of Certified Reference Materials, Reference Materials, and Analytical standards to the market. Activities are aligned with ISO 9001, ISO/IEC 17025, and ISO 17034.
  • Author the MANGO document for Audit purposes.
  • Undertake assigned projects, stability studies, writing of reports, and batch records related to Certified Reference Material.
  • Product & Application Development: process and evaluate analytical QC data generated primarily by GC and HPLC.
  • Follow regulatory, customer, and quality system requirements in product development.
  • Write reports on the results of project work, document methods on project/product design, test specifications, etc.
  • Collaborate and work with other staff (Scientists and Technicians) remotely to complete QC data generation and analysis on Certified Reference Materials.
  • Participate in training colleagues for technical transfer. Work with the team and other departments to implement validation and tech transfer requirements.
  • Contribute to project planning through communication with the manager, project manager, and team:
    • Identify and communicate resource requirements for specified projects.
    • Provide timely updates and communicate project status to management and the project team.
    • Communicate promptly issues related to schedule, planning, and resources that may stall or prevent the execution of the project.

Technical Expertise:

  • Operation of chromatographic instrumentation, including HPLC and GC.
  • Operation of chromatographic detectors, including UV-Vis, RI, MS, ELSD, ECD, FID, and others.
  • Processing chromatographic data using chromatographic software.
  • Utilizing Microsoft Excel to perform calculations.
  • Develop and expand technical and subject matter expertise in assigned technical areas by seeking out training and knowledge-sharing.
  • Technical project review of certificates for certified reference materials by mass balance techniques that may be traceable to primary pharmacopeias.

Documentation:

  • Write reports on results of project work, document methods on project/product design, test specifications, write batch records, etc., for transfer to QC.
  • Maintain batch records and other documentation.

Requirements

  • Education: A bachelor’s degree in chemistry, chemical engineering, or other related scientific discipline. 1 year of relevant experience in a scientific laboratory.
  • Demonstrated proficiency in basic analytical GC and HPLC techniques.
  • Basic understanding of the relevant subject matter field (e.g., organic chemistry, analytical chemistry, process chemistry).
  • Demonstrated initiative and critical thinking to learn new skills and technologies.
  • Strong verbal and technical writing skills.
  • Ability to utilize a variety of software tools involving databases, spreadsheets, and project scheduling.
  • Ability to work independently and prioritize assigned work.

APPLY ONLINE HERE

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