Job Overview
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Date PostedAugust 19, 2023
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Location (State / UT)
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Expiration dateAugust 18, 2024
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Experience5 Years, 10 Years
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GenderAny
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Desired QualificationMaster’s Degree, Bachelor Degree
Job Description
Key responsibilities:
- Well, understanding of basic Project Management principles viz. process groups, and knowledge areas.
- In-depth knowledge of pharmaceutical formulation and regulatory requirements & guidelines.
- Operational interface with Core teams, CFTs, collaborators, stakeholders, and service providers to ensure timely execution.
- Keeping track of Project milestones, project costs, detailed timelines, and issue logs after Project initiation.
- Provide weekly updates on status, issues, and challenges to all stakeholders and senior management.
- Conducting teleconferences and circulation of action points/minutes to customers/team members.
- Coordinate project execution, track and report on progress to the project team, stakeholders, and management.
- Executing and evaluating projects according to predetermined timelines.
- Follow-Up from Technical Services, DRA, Supply chain, Quality, and Manufacturing teams for keeping project Scope and its Scheduling within a time frame.
- Well-versed with in-house and outsourced CMO & CRO operations.
- Coordination with Clinical Pharmacology Dept. slotting or Bio studies, availability results, and reports.
- Coordinate project development and filing of dosage forms.
- Review projects and identify early warning signals and on-time escalations.
- Present the status of each project during monthly and quarterly project reviews.
- Preparing MIS reports like Project status reports, project risks, batch planners, resource utilization reports, etc.
- End-to-end responsibility for delivery of all allocated Projects as per filing/Launch dates.
- Prioritize the project schedule in line with the organizational goals.
Qualification: B.Pharma, M.Pharma