Job Location: Translational Health Science and Technology Institute (TSHTI) - Faridabad, Haryana
Department: Human Pharmacology Unit - Translational & Clinical Research
About Syngene: Syngene (www.syngeneintl.com) 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 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
Hold self and their teams accountable for the achievement of safety goals
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Govern and Review safety metrics from time to time
Role Accountabilities:
Computer System Validation
Support validation activities for GxP computerized systems and applications.
Prepare, review, and maintain CSV lifecycle documentation including:
Validation Plans (VP)
User Requirement Specifications (URS)
Functional Specifications (FS)
Risk Assessments
Traceability Matrix (TM)
Installation Qualification (IQ)
Operational Qualification (OQ)
Performance Qualification (PQ)
Validation Summary Reports (VSR)
Execute and document validation testing activities.
Regulatory Compliance & Quality
- Ensure compliance with:
US FDA 21 CFR Part 11
EU Annex 11
GAMP 5 Guidelines
Data Integrity requirements
GxP regulations (GCP, GLP, GMP)
Support Electronic Records and Electronic Signatures (ERES) assessments and remediation activities.
Participate in Data Integrity assessments and compliance initiatives.
Assist in maintaining systems in a validated state through change management activities.
Quality Management System (QMS)
Support investigation, documentation, and closure of:
Deviations
CAPAs
Change Controls
Audit Observations
Participate in periodic review activities for computerized systems.
Ensure validation deliverables comply with internal procedures and quality standards.
Audit & Inspection Support
Support internal, customer, and regulatory audits.
Assist in preparation and presentation of CSV documentation during audits and inspections.
Support remediation activities related to audit findings.
Syngene Values
All employees will consistently demonstrate alignment with our core values
Excellence
Integrity
Professionalism
Experience: 6 to 13 Years
Education: Master’s in Science (M.Sc.)
Equal Opportunity Employer:
It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.
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