Executive Jobs at Syngene | MSc Analytical Chemistry Jobs
Executive Jobs at Syngene. Syngene, a leading innovation-driven CRDMO, is hiring a Senior Executive, QA (Analytical QA Analyst), at its Bangalore facility. This opportunity is ideal for experienced analytical chemistry and pharmaceutical professionals who are passionate about quality systems, cGMP compliance, data integrity, and regulatory excellence in a safety-driven research environment. Interested candidates apply for the exciting opportunity at Syngene Careers.
About Syngene:
Syngene is an innovation-led contract research, development, and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety on par with business performance through shared responsibility and accountability, including adherence to safety guidelines, procedures, and SOPs in letter and spirit.
- Position: Senior Executive QA
- Date: 7 Jan 2026
- Location: Bangalore, KA, IN, 560099
- Division: Dedicated Centre
JOB DESCRIPTION
- Job Role: Analytical QA analyst
- Department: Quality Assurance – BGRC
- Job Location: Bangalore
Mandatory Expectation 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 training related to data integrity, health, and safety measures is completed on time by all team members, including oneself.
- Compliance with Syngene’s quality standards at all times.
- Hold themselves and their teams accountable for achieving safety goals.
- Govern and review safety metrics periodically.
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 verification.
- 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, such as EAM, IT, etc.
- Issue documents from the EDMS and reconcile them.
- 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, 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 results in non-conformity or observations due to a lack of review against the defined procedure.
- Ensuring approved documents have no gaps, including compliance related to good documentation practices.
- Execution and approval of ISO 17025:2017 requirements at BGRC.
Specific Requirements for This Role
Experience
- Foundational
Behavioural Skills
- Good interpersonal skills
- Self-time management
- Good team player
- Good communication skills
Education
- M.Sc/ M.Pharma (Analytical Chemistry/Chemistry)
