Job Reference: JO-2404-66651_1712748351
Summary:
Responsibilities:
- Coordinate site project team to deliver biological projects.
- Develop realistic cross-functional implementation plans with input from above site and site functions (R&D, Engineering, Manufacturing, Quality, Regulatory, Commercial, Supply Chain, Finance, HR.
- Utilize the relevant PMO tools for project planning, monitoring, and reporting.
- Set project milestone and report progress accordingly. Consider alternative approaches and take corrective actions as needed to ensure project milestones are achieved.
- Provide program management support for and guide the efforts of third-party organisations (vendors, suppliers, contractors, etc..) to enable the achievement of shared milestones.
- Fulfil management role in terms of organising project teams, facilitating communication between resources, guiding technical, financial, business and personnel conflict resolution and monitoring budget administration.
- Identify and implement opportunities that will improve the site's ability to implement and manufacture quality products in a cost-effective, compliant, and timely manner.
- Other duties as assigned.
Requirements:
- Degree in Engineering, Science business, Project management or related discipline
- 5 years of diversified Pharma / Bio business experience: operations support, quality, supply chain, validations, capital and expense management, commercial product launches
- PMI certification is desirable.
- Ops experience in Sterile Manufacturing
- Previous experience in setting up new Bio processes / equipment / plants and/or NPI.
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The Life Science Specialists