Recent QA Jobs at Syngene | MSc Analytical Chemistry Candidates Apply Now

Recent MSc Analytical Chemistry Jobs at Syngene

Are you looking for analytical QA jobs in Bangalore with a global research and development leader? Join Syngene International, an innovation-driven contract research, development, and manufacturing organization. As an Analytical QA Analyst, you will ensure compliance with cGMP, data integrity, and ISO standards while supporting scientific excellence in a collaborative environment.

About Syngene

Syngene International Ltd. is a leading innovation-led contract research, development, and manufacturing organization (CRDMO) offering integrated scientific services from early discovery to commercial supply. With a strong focus on safety, integrity, and quality, Syngene empowers professionals to grow and contribute to global scientific advancements.

Job Details

  • Job Role: Analytical QA Analyst
  • Location: Bangalore, KA, India
  • Department: Quality Assurance – BGRC
  • Experience: 2–6 years
  • Education: M. Pharm / M.Sc. in Analytical Chemistry or Chemistry

Core Purpose of the Role:

  • The employee is responsible for the following activities:
  • Responsible for online documentation, adhering to GDP practices.
  • Authorized to prepare quality assurance procedures.
  • Attend mandatory training as and when conducted.
  • Responsible for archival activities.
  • Responsible for the execution of daily QA activities and the maintenance of the area.
  • Authorized to issue documents from EDMS and reconcile the same.
  • Authorized for issuance and withdrawal of logbook, procedures, schedules, etc.
  • wherever applicable, and maintenance of issuance/ withdrawal records.
  • Responsible for monitoring the usage of current approved procedures in all relevant departments.
  • Responsible for overall management of training activities and handling of training.
  • Authorized to perform training coordinator responsibilities as per procedure.
  • Responsible for ensuring compliance with cGMP as laid down in the procedures.
  • Responsible for ensuring safe operation within BGRC QA and accordingly to ensure zero safety incidents.
  • Ensure to report safety incidents/ Near misses, if any, and 100% safety-related training compliance.
  • Responsible for the maintenance of the QA SOP index and specimen signatures of new joiners.
  • Responsible for escalating the abnormalities/ gaps in procedures, if any, to the reporting manager/ HOD or user department (where applicable).
  • Responsible for the execution and approval of ISO 17025:2017 requirements at BGRC. Any other assignment allocated by the reporting manager and/or above.

Behavioural Skills

  • Strong interpersonal and communication skills
  • Self-time management and organizational ability
  • Team-oriented with a positive, collaborative mindset

Why Join Syngene?

  • Work with a global leader in contract research and manufacturing.
  • Contribute to high-impact pharmaceutical and biotechnology projects.
  • Grow your career in a culture of excellence, integrity, and professionalism.
  • Access cutting-edge facilities and continuous learning opportunities.

APPLY ONLINE HERE

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