About PSC Biotech
Who are we?
PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.
‘Take your Career to a new Level’
PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.
Employee Value Proposition
Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client’s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.
Overview:
We are seeking an experienced and highly organized Project Manager to join our team in Ireland. In this role, you will lead cross-functional projects that support the development, manufacturing, and/or commercialization of innovative biotechnology products. You will be responsible for planning, executing, and delivering projects on time, within scope, and within budget while ensuring alignment with business objectives, quality standards, and regulatory requirements.
Key Responsibilities:
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Lead and manage multiple complex projects from initiation through completion
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Develop project plans, timelines, milestones, budgets, and resource requirements
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Coordinate cross-functional teams, including EPCM partners, Trade Partners manufacturing, quality, regulatory, supply chain, and commercial stakeholders
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Monitor project progress, identify risks, and implement mitigation strategies
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Facilitate regular project meetings, status updates, and stakeholder communications.
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Ensure project deliverables meet company standards, compliance requirements, and regulatory expectations
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Manage dependencies, change requests, and issue resolution effectively
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Track KPIs, project outcomes, and lessons learned for continuous improvement
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Support vendor and external partner coordination as needed
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Prepare executive-level updates, reports, and presentations
Education/Experience Requirements:
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Minimum qualification B.Sc. or M.Sc./ M. Eng Degree in Engineering
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Minimum of 12 years post academic engineering experience in relevant aseptic/sterile processing design and start-up environment
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Extensive Project Management experience
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Demonstrated ability to be a team player
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Excellent communication/presentation/organizational skills
Notes:
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This is a contract position. Estimated assignment duration is approx. 12 months.
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The position is based full-time onsite at the Dunboyne or Swords with requirements to visit Dunboyne, Swords and Dundalk on a regular basis. Flexibility is required in this regard.
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Looking for candidates who are willing to work as Limited Contractors only (LTD)
