QA Jobs at Syngene | MSc Chemistry Graduates Apply Now
Are you looking for a rewarding QA job in a world-class research environment? Syngene International is offering an exciting opportunity for chemistry professionals through its Senior Executive QA role in Bangalore. This position is ideal for candidates exploring Syngene careers, especially those seeking Chemistry Jobs in Bangalore with strong growth potential, advanced lab exposure, and a culture built on safety, quality, and scientific excellence.
About Syngene
Syngene International is a leading global contract research, development, and manufacturing organization delivering integrated scientific solutions from early discovery to commercial supply. Known for its world-class research facilities and strong quality standards, Syngene offers an excellent platform for professionals seeking a rewarding QA job or advanced Chemistry Jobs in Bangalore. The company fosters a culture of safety, innovation, and scientific excellence, making it a preferred choice for individuals looking to build long-term Syngene careers. With cutting-edge technology, skilled teams, and global client partnerships, Syngene continues to drive impactful scientific progress across multiple industries.
Position Details
- Job Title: Senior Executive QA
- Location: Bangalore, KA, IN, 560099
- Education: M.Sc/ M.Pharma (Analytical chemistry/Chemistry)
Mandatory Expectations for All Roles as Per Syngene Safety Guidelines
- Overall adherence to safe practices and procedures of oneself and the teams is aligned.
- Contributing to the development of procedures, practices, and systems that ensure safe operations and compliance with the company’s integrity & quality standards.
- Driving a corporate culture that promotes an EHS mindset and operational discipline at the workplace at all times.
- Ensuring the safety of self, teams, and lab/plant by adhering to safety protocols and following environmental, health, and safety (EHS) requirements at all times in the workplace.
- Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team, including oneself.
- Compliance with Syngene’s quality standards at all times.
- Hold self and their teams accountable for the achievement of safety goals.
- Govern and review safety metrics from time to time.
Core Purpose of the Role
- Online documentation adhering to GDP practices.
- Review and approval of protocols and reports (Method validation, Method Verification, Method Transfers, Study, Compounding Stability).
- Review and approval of analytical documents (blank ODS, executed ODS, summary sheets, specifications, results, analyst qualifications, etc.).
- Ensuring cGMP is followed in QA and QC.
- Overall functioning of the respective QC team activities.
- Preparation and review of QMS trend reports.
- Review and approval of instrument/equipment Qualification and calibration data.
- Perform and approve periodic audit-trail verifications.
- Review and approval of quality assurance procedures.
- Preparation of Quality assurance procedures.
- Review and approval of quality control and CFT procedures.
- Coordinate and investigate QMS.
- Training of personnel in Quality Control, Quality Assurance, and other CFTs (wherever necessary).
- Attend mandatory trainings as and when conducted.
- Ensure effective archival activities.
- Execution of daily QA activities and maintenance of the area.
- Regular client interaction via telecom or e-mail.
- Implementation of corrective and preventive actions and monitoring their effectiveness (wherever applicable).
- Review and approval of CFT documents like EAM, IT, etc.
- Issue documents from EDMS and reconciliation of the same.
- Perform the initiator / QA reviewer role in Trackwise.
- Perform reviewer / approver role in EDMS.
- Collate and prepare slides for the QRM Metrics meeting.
- Prepare, review, and approve planners.
- Issuance and withdrawal of logbook, procedures, schedules, etc., wherever applicable, and maintenance of issuance/ withdrawal records.
- Monitoring the usage of current approved procedures in all relevant departments.
- 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.
- Escalating the abnormalities/gaps in procedures, if any, to the reporting manager/ HOD or the user department (where applicable).
- Ensuring no document is reopened or leads to non-conformity or observation due to a lack of review against the defined procedure.
- Ensuring approved documents have no gaps, including compliance with good documentation practices.
- Execution and approval of ISO 17025:2017 requirements at BGRC.
Syngene Values
- Excellence
- Integrity
- Professionalism
Specific Requirements for This Role
Experience
- Foundational
Behavioural Skills
- Good Interpersonal skills
- Self-time management
- Good team player
- Good communication skills
