Your Impact
In this role you will be responsible for project delivery, design management & project management, for positioning and winning projects involving a range of services. The role will be instrumental in collaborating with commercial, project management, engineering and design technical leaders to create opportunities for Jacobs to plan, develop, deliver and operate a range of projects. "
Sr. Engineer CQV
Role : Permanent
Gurgaon/ Mumbai/ Hyderabad/ Bangalore/Pune
CQV Engineer
Role and Responsibilities:
The C&Q Engineer shall be responsible for carrying out the following project related activities:
- Good Experience in Master Planning and scheduling the project.
- Preparation of documents associated with lifecycle of C&Q activities for URS, TM, IC, OC, IV, IQ, OQ & PQ.
- Preparation and execution of FAT, Commissioning and SAT protocols
- Preparation and execution of Qualification protocols (IQ and OQ)
- Design Review (DR) and Design Qualification (DQ) protocol preparation, execution and follow-up
- Field Walkdowns of systems as part of transfer of ownership of the system from Construction
- Ensuring safe operation of the system prior to and during start-up functional testing and Qualification phases
- Installation Verification execution
- System Startup activities
- Functional Testing of systems
- CIP and SIP Validation and Cycle development for the same.
- TOP Review and Compilation
- Handling of Punch Lists, Deviations and Change Management activities during project lifecycle
- Commissioning & Qualification Report writing
- Organize and review daily tasks/verifications and track the progress of the activities assigned
- Contractors and/or Vendors coordination
- Interfacing with representatives on project team, Construction, Engineering, Automation, Quality and End Users during the different project phases.
Qualifications Key Competencies:
- Degree or equivalent in an Engineering/ Science related discipline/ B. Pharmacy
- Strong leadership and team player ability, liaising directly with client and other project key functions
- Previous experience as working and leading C&Q team
- Strong knowledge of ISPE and ASTM E2500 and various regulatory GMP guidelines
- Proven experience with international pharmaceutical projects
- Mentor for junior staff members
- Self-starter & good team player
- Good oral & written communication skills
With safety and flexibility always top of mind, we’ve gone beyond traditional ways of working so you have the support, means and space to maximize your potential. You’ll uncover flexible working arrangements, benefits and opportunities to do good too – from participating in our global giving and volunteering program, to exploring new and inventive ways to help our clients make the world a better place. No matter what drives you, you’ll discover how you can cultivate, nurture and achieve your goals – all at a single global company.
