Job Title:
Job Location:
About Syngene :
At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit
Mandatory expectation for all roles as per Syngene safety guidelines
- Overall adherence to safe practices and procedures of oneself and the teams aligned
- Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards
- Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
- Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, 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 self
- Compliance to Syngene s quality standards at all times
Core Purpose of the Role:
- Providing line clearance before starting of batch, product change over.
- Providing line clearance for dispensing of raw materials.
- Verification of Raw materials and consumable for correct status labelling and storage conditions.
- Monitor critical parameters during manufacturing.
- Assessment of breakdowns of the equipments.
- Review and approval of Batch Manufacturing Records (BMR), SOPs, Protocols, Reports, Risk assessments etc.
- Issuance and control of documents like Logbooks, SOPs, Annexures, BMRs, Protocols etc.
- Periodic review of EMS reports.
- Vial (Cell banks) issuance, receipt and periodic reconciliation.
- Handling of QMS Deviations, Incidents, CAPA and Change Control.
- Monitor cleanroom parameters like temperature, humidity, and differential pressure.
- Ensure real-time documentation and compliance with GDP.
- Perform Audit trails for GXP computerized systems.
- Maintain Readiness of Regulatory and Internal quality audits.
- Participate in Process validation and Cleaning validations activities, to verify the adherence of validation protocols and documentation.
- To ensure storage chambers are maintained at set temperature limits and take timely action in case of any excursions.
- To ensure the instrument/equipment are in calibrated state.
- Ensure the breakdowns if any are rectified in time and instrument is made up and running within shortest possible time in co-ordination with service provider.
- Ensuring all time audit readiness and preparation prior to audits.
- Ensuring completion status of action items of CAPAs triggered through observations of previous audits.
- To support any other activity allotted by the team lead.
Role Accountabilities:
- Seamless operations in coordination with team leader
- Error free analysis
- Timely completion of tasks
Syngene Values
- Integrity
- Professionalism
Specific requirements for this role
Experience:
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Demonstrated Capability-
- Knowledge on Biologics Manufacturing.
- Knowledge on Regulatory guidance, Audits and readiness
- Good knowledge in MS Office tools.
- Good understanding in QMS
- Excellent communication skills (written and oral).
- Co-Operation with team leads
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Education - M. Sc. (Chemistry/Biochemistry/B. Pharm/M. Pharm/Biotechnology)
Skills and Capabilities:
- Good understanding in QMS.
- Handling a small Team.
- Basic knowledge in SAP. Having Track wise experience is a plus.
- Excellent communication skills written and oral.
Equal Opportunity Employer
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