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| Job Location | Delhi |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Management Consulting / Strategy |
| Functional Area | General / Other Software |
| EmploymentType | Full-time |
Job Brief:
Seeking a CSV Consultant to work on a variety of validation projects including manufacturing systems, lab systems, risk Assessments, etc. Some of the work may be done remotely, some at client sites and other at one of our offices.
Job Responsibilities:
Responsible for the Computer System Validation processes of the company
Maintain expertise in current and emerging cGMP requirements and quality trends (e.g., 210, 211, 820, and 21 CFR Part 11).
Work independently on and successfully solve problems and complete/qualify a system within given constraint of scope, time and schedule.
Lead system qualification efforts and be the primary client contact for coordinating work, reporting status, resolving issues, and addressing change orders as they apply.
Minimum Requirements:
Minimum degree requirement - Bachelors degree with atleast 10+ years of experience
Must be willing to travel regionally and/or nationally throughout India
Candidates must have excellent verbal communication and technical writing skills.
Experience in generation and execution of protocols and procedures, related to different
Candidates must demonstrate expertise in ISPEGAMP5, ICH Q8, ICHQ9, ICH Q10 and 21 CFR part 11, Computerized System Validation, Equipment
Qualification and Working knowledge of the development of protocols for the Validation of complex computer systems (e.g., multiple GAMP classes of systems); Protocol development will include ability to develop Installation, Operational and Performance qualification
Experience in execution of system validation lifecycle deliverables
Experience in project execution within at least one area of systems validation
(e.g.,laboratory equipment, facilities utilities, manufacturing equipment)
Proficient in Microsoft Word, Excel, Power Point and Project
,Keyskills :
protocol developmentproject executioncontinuous improvement facilitationmanufacturing systemscomputer system validationtechnical writingresolving issuesmicrosoft wordcfrriskchange orderscomputerized system validation21 cfrclient contactcgmp