C&Q Planner

1 week ago

Singapore No deviation Full time

Join to apply for the C&Q Planner role at No deviation At No deviation, we are dedicated to delivering patient‐centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation. We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That is why we foster a culture of collaboration, inclusion, and continuous development – empowering our team members to grow personally and professionally. Position 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. 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. Required 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. Why join us?Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company. Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated. Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career. How To Apply Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team Please submit your resume, outlining your qualifications and experience relevant to the role, here. #J-18808-Ljbffr

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