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.
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