Project Leader / SME for PP/QM/ATTP

Purpose of the Role :The IT project leader leads IT projects from initiation to business value realization, designs and implements information processes and systems, acts as Subject Matter Expert, and develops the portfolio according to IT and business strategy.

Key Responsibilities

Manages projects Engineers' business processes Prioritizes and challenges changes in line with IT strategy Acts as Subject Matter Expert Manages IT systems lifecycle Maintains process, technical and training documentation Performs testing and validation Organizes functional forums and trains trainers Provides second line support Develops IT landscape with BPOs and IT partners Delivers projects on time, in budget and according to specifications and compliance (CSV) Integrates processes across business domains Leadership Behaviors:Communicates effectively with a diverse audience. Leads project teams, learns quickly, works collaboratively, and demonstrates intercultural awareness.Decision Rights and AccountabilityAccountable for IT project portfolio outcomes. Negative project performance may impact business goals and project delivery.KPIsDeliver projects on time, within budget, and according to specifications. Provide stable IT systems

Required Competencies

Strong knowledge in QM, PP and ATTP (serialization)Strong project management skills. Delivers project on time, in budget and according to specifications.Independent and reliable workerTeam player.Strong communications skills.Intercultural skills.Pharma experience exposure to CSVMinimum years of experience:15+ years.Education RequiredBachelor's Degree in Engineering, Information Technology, Computer Science, Pharmaceutical Sciences, or a related disciplineMaster's Degree (MBA, M.Tech, or equivalent) is preferredSAP Certification in PP (Production Planning), QM (Quality Management), or ATTP (Advanced Track & Trace for Pharmaceuticals) is an added advantageTraining or certification in Project Management (PMP, PRINCE2, Agile/Scrum) is desirablePreferred Industry BackgroundPharmaceutical, Life Sciences, Manufacturing, or Supply Chain domain experienceKnowledge of Computer System Validation (CSV) and GxP regulations preferred