- અનુભવ
- કોઈપણ
- પગાર
- —
- ઓપનિંગ્સ
- 1
- પોસ્ટ કર્યું
- એક કલાક પેહલા
- કાર્ય મોડ
- ઓફિસમાં
- ફરી શરૂ કરો
- અરજી કરવી જરૂરી છે
તમે ક્યાં કામ કરશો
કામનું વર્ણન
Job Overview
Become a key contributor within a prominent global pharmaceutical manufacturer committed to sustainability and societal welfare. In this role, reporting to the Engineering Projects & Systems Lead, you will be responsible for managing CAPEX and non-CAPEX engineering projects from conception through to final delivery. This position offers the chance to take full ownership of project timelines, budgets, and leading cross-functional teams within a forward-thinking and collaborative environment.
Key Responsibilities
- Manage engineering projects comprehensively, including conducting feasibility assessments, defining objectives, scheduling, and allocating resources.
- Oversee financial aspects, maintaining accountability for project budget and cash flow control.
- Provide leadership by inspiring and directing both internal teams and external contractors or vendors.
- Lead cGMP validation activities and prepare lifecycle documentation such as URS, FDS, FAT, SAT, IQ/OQ, and conduct Risk Assessments.
- Support systems management by maintaining MES-managed documentation including System Configuration and Descriptions.
- Ensure proper handover to business units under controlled conditions and perform post-project reviews to facilitate continuous improvements.
Candidate Profile
Essential qualifications and experience:
- Experience in project engineering, management, or validation within pharmaceutical manufacturing settings.
- Proven success in delivering engineering projects and equipment installations on schedule and within budget.
- Strong financial understanding related to engineering project execution.
- Comprehensive knowledge of project lifecycles from initial concept through to qualification phases.
- Excellent communication, analytical, problem-solving, and time management abilities, capable of managing priorities in dynamic environments.
Preferred attributes:
- Hands-on experience with drug manufacturing processes.
- Exposure to cGMP start-up environments is advantageous.