Life Science Jobs | Syngene is Hiring a Team Member | Apply Now
Are you seeking impactful life science jobs in a globally respected organization? Syngene International Ltd. is inviting applications for the role of Validation and Qualification Team Member in Bangalore. This opportunity is ideal for professionals looking to strengthen their quality assurance jobs profile while building a long-term Syngene career in pharmaceutical validation, compliance, and corporate quality systems.
Job Details
- Job Title: Validation/ Qualification Team Member
- Location: Bangalore, KA, IN, 560099
- Division: Essential Functions
- Department: Corporate Quality Assurance
About the Company
Syngene International Ltd., established in 1993, is a global innovation-driven research, development, and manufacturing organization. The company supports pharmaceutical, biotechnology, nutrition, animal health, and specialty chemical industries worldwide. Syngene collaborates with leading global clients and delivers integrated scientific solutions across the product lifecycle. With a strong emphasis on quality, compliance, and innovation, Syngene provides meaningful life science jobs. A Syngene career offers stability, growth, and global exposure in quality-focused environments.
Key Responsibilities
- Preparation and review of equipment, utility qualification relevant procedure and ensuring execution compliance as per approved SOP.
- Responsible for preparation of protocols (if applicable) and reports in line with site-specific SOP for chemical development facility.
- Review of procedures, URS, impact assessment, risk assessment, protocols & reports for qualification & validations for facility/Area, equipment, utilities in facilities, re-qualification documents, and QMS documents in compliance to approved procedure.
- Coordinate the activities of qualification/validation with the stakeholder departments, ensuring the timely completion of projects and project milestones.
- Ensure CQA validation oversight during FAT, commissioning/SAT and IQ, OQ & PQ as per qualification requirements & documentation.
- Review of design documents and execution of IQ, OQ and PQ activity of the new facility/product/process critical equipment along with documentation in place in time as per defined procedure.
- Review of facility, utility related drawings/layouts (for example, pressure differential, AHU zoning, area classification, equipment layouts, piping drawings, isometric drawings etc.).
- Ensure CQA validation oversight during periodic validation of critical process equipment, utilities such as HVAC systems, water system and compressed air systems revalidations.
- Supporting to prepare VMP calendar. Ensuring execution of re-qualification activities as per VMP calendar tolerance.
- Support external client audits and regulatory inspections.
Educational Qualification
MSc/ BTech/ BSc
Technical/Functional Skills
- Technical knowledge in Biologics is preferable.
- Technical knowledge in API and Formulation are add-on value.
- Should have experience in Pharmaceutical Validation systems (Facilities, Utilities, Equipment, and Computerized Systems).
- Manufacturing Computerized System Validation (CSV)/Process Control System deliverable preparation/review.
- QMS procedures.
- Should be knowledgeable on validation guidelines per different regulatory requirements and Industrial bodies, e.g., ICHQ2, ICH Q7, WHO, US FDA, EU guidelines, 21 CFR, ISPE, PDA, and PICS.
- Interpersonal skills to establish collaboration with cross-functional teams.
- Establish good interpersonal skills with cross-functional teams.
Behavioural Skills
- Should have good communication skill and should be a good team player.
- Ability to work successfully in a dynamic, ambiguous environment.
- Ability to meet tight deadlines and prioritize workloads.
Competences
- Excellent written and verbal communication skills
- Good interpersonal skills
- Analytical strengths and high trouble shooting ability
This role is an excellent opportunity for professionals targeting structured quality assurance jobs within regulated industries. Joining Syngene allows you to strengthen validation expertise while contributing to high-quality scientific outcomes. If you are focused on long-term growth through life science jobs with global exposure, this Syngene career opportunity is a strong next step.
