Assignment Details
Our Client a specialized drug development and manufacturing company is looking to engage with a PMO consultant in pharmaceutical industry for a project.
Roles and Responsibilities:-
-Lead and manage pharmaceutical projects from initiation to completion, ensuring adherence to timelines, budgets, and quality standards.
-Coordinate and collaborate with CFTs, including Manufacturing, Quality Control (QC), Quality Assurance (QA), and Supply Chain teams.
-Ensure compliance with regulatory requirements for regulated markets and facilitate seamless project execution.
-Oversee analytical method development, validation, and technology transfer activities.
-Manage registration batch execution and documentation, ensuring alignment with filing requirements.
-Track project progress, identify potential risks, and develop mitigation strategies to ensure successful project outcomes.
-Facilitate communication and stakeholder engagement across teams to maintain transparency and efficiency.
-Work closely with regulatory teams to ensure timely and accurate filing of product registrations.
-Monitor and report project KPIs, providing regular updates to senior management.
-Drive continuous improvement initiatives within project management processes.
NOTE:
Duration-6 months(Extendable)
Location- Obedenhalli, Bangalore
Capacity-Full Time, Onsite
Skills Required
-Project management experience in the pharmaceutical industry.
-Strong understanding of regulatory requirements for global markets.
-Experience managing projects related to analytical methods, registration batches, and -regulatory filings.
-Excellent leadership, problem-solving, and stakeholder management skills.
-Proficiency in project management tools and methodologies.
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8 month(s)
8+ years 
On-Site
