CQV Manager
- Mumbai, Maharashtra
- Permanent
- Full-time
Works with IPS CQV/Project management team to develop and apply quality practices for all project
deliverables and business practices. In conjunction with the Project management team, performs project
audits to ensure all project goals are being met and compliance services are offered as a value-added
product to IPS’ clients.
Promote efficiency in staff utilization. Manages and assigns regional resources to meet project
requirements. Works with other Regional Managers and other IPS disciplines to maintain targeted /
budgeted utilization. Tracks staff assignments, makes resource projections, and makes necessary
adjustments as required. Prepares workload forecasts to support staffing management.
Leads, mentors, trains, and manage team of compliance staff assigned to the respective regional office.
Assists and mentors’ staff to set performance and career goals. Provides routine feedback and conducts
formal time-based performance reviews. Implement corrective action plans as required.
Generates and performs C/Q/V deliverable activities, audits, and other compliance services as required, to
meet project requirements and personal billability goals. Works with potential new and existing clients to
initiate projects following current industry practices. Performs strategic and master planning activities to
assure projects are initiated/started “on the right foot”.
Preparation of project monthly report, Management of various GEP and GMP documents, QMS
Document review and Gap analysis
Ensures the quality, accuracy, and completeness of overall work as to CQV Department, compliance with
established IPS and client standards, procedures, codes, and ordinances.
Guidance for implementation of Biotech/Pharmaceutical industry standards in generating and updating
supporting documentation such as P&IDs, material and equipment specifications / datasheets, and user
requirement specifications
Track Quality deliverables by strong interaction with inhouse team, clients & vendors Qualifications & Requirements:Must be able to demonstrate competency in performing the responsibilities of a CQV Manager
Bachelor’s degree in engineering or a related field preferred
A minimum of 10 years (Manager) to 15 years (Director) of experience in Pharmaceutical, Biotech, Medical
Device Design, Construction, Commissioning, Validation, or QA. Experience in writing and execution of PFC,
FC, IQ, OQ, and PQ forms and protocols for GMP Utilities, Equipment, Systems, and Software.
Experience with Cleaning, Process, Computer System, Methods and other validation activities and processes.
Detailed experience in the discipline of GMP/Validation with a knowledge and understanding of
pharmaceutical Design/Build/Commission/Validate processes and how they relate to regulatory requirements
and cGMP regulations
Progressive ability, capacity, and aptitude in administration to plan, organize, supervise, and coordinate
technical work and to obtain cooperation from others. Analytical thinking, structured problem-solving skills,
superior communications skills, team building and strong work ethics. Must be able to build rapport with
department staff