Planning Engineer

4 days ago


Singapore Leap29 Full time

Direct message the job poster from Leap29Recruitment & Compliance | Change Management (CPD) | Process & Crisis Resilience | Content Creator | Visa & Audit Lead (UK/NL/SP)C&Q Planner Duration: 6 month contract (potential to extend)Overview The C&Q Planner plays a critical role in ensuring the timely and compliant execution of commissioning and qualification activities for pharmaceutical manufacturing facilities, equipment, and systems. This role supports GMP-compliant project delivery by developing and managing integrated schedules, coordinating cross‐functional teams, and ensuring alignment with regulatory expectations and project milestones. We are seeking a highly motivated and detail‐oriented professional who thrives in a collaborative environment and is passionate about delivering high‐quality results in a regulated industry. Key Responsibilities Develop and maintain detailed C&Q schedules using project planning tools (e.g., MS Project), aligned with overall project timelines. Collaborate with engineering, validation, QA, QC, and operations teams to plan and sequence commissioning and qualification activities. Monitor progress, identify schedule risks, and implement mitigation strategies to ensure timely delivery of C&Q milestones. Support the development and execution of C&Q strategies, including URS, DQ, IQ, OQ, and PQ documentation and activities. Ensure C&Q activities comply with GMP, FDA, EMA, and other applicable regulatory standards. Facilitate planning meetings, progress reviews, and reporting to project stakeholders. Coordinate resource planning and availability for C&Q tasks, including vendor and contractor support. Maintain accurate documentation and change control records related to C&Q scope. Support audits and inspections by providing schedule‐related documentation and insights. Qualifications Bachelor’s degree in Engineering, Life Sciences, or related field. Minimum 3 years of experience in project planning within a GMP‐regulated pharmaceutical environment. Strong understanding of C&Q processes and lifecycle documentation (URS, DQ, IQ, OQ, PQ). Proficiency in project scheduling software (Primavera P6, MS Project, etc). Familiarity with ISPE Baseline Guides and industry best practices for C&Q. Excellent communication, organizational, and stakeholder management skills. Preferred Skills PMP or equivalent project management certification. Experience with large‐scale pharmaceutical capital projects (e.g., new facility builds, equipment upgrades). Knowledge of computerized systems validation (CSV) and data integrity principles. Experience with digital validation platforms (e.g., KNEAT) or eQMS systems. If you are a team player with a passion for excellence and a commitment to delivering results in a collaborative environment, we encourage you to apply for this exciting opportunity. #J-18808-Ljbffr


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