
Senior Pharmaceutical Engineer Scheduling Specialist
1 week ago
This role plays a vital part in ensuring the timely delivery of pharmaceutical engineering projects, maintaining quality, safety, and regulatory compliance standards.
- Schedule Development:
- Create comprehensive master schedules using Primavera P6 or MS Project, integrating inputs from design, procurement, construction, and validation teams.
- Sequence activities based on pharmaceutical process logic and workflows.
- Progress Monitoring & Control:
- Update site progress weekly, tracking critical paths and buffer times.
- Identify risks of delay and support mitigation or recovery strategies.
- Manage milestone schedules, especially those tied to equipment installation and validation.
- Reporting & Communication:
- Produce weekly/monthly progress reports and 3-week lookahead schedules.
- Present scheduling updates during internal and client meetings.
- Assist in preparing Time Impact Analysis (TIA) and claims documentation.
- Risk Management & Coordination:
- Participate in project risk reviews, incorporating schedule-related risks into the risk register.
- Collaborate with construction, safety, and logistics teams to optimize activity sequencing.
Requirements:
- Bachelor's degree or higher in Engineering, Construction, or Project Management.
- At least 5 years of scheduling experience, with 3+ years in pharmaceutical projects.
- Proficient in Primavera P6; skilled in MS Project and Excel for schedule analytics.
- Familiarity with GMP processes and cleanroom construction sequencing.
- Knowledge of Singapore's construction regulations (BCA, MOM, SCDF) and site safety standards.
- Excellent communication and collaboration skills, with ability to work on-site.
Qualifications:
- PMP certification.
Reporting Structure:
- Reports directly to the Project Manager.
- Interfaces with Design, Procurement, Construction, Validation, and Client teams.
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