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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.
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:
The Project Scheduler will be responsible for developing and maintaining a detailed, resource-mapped Site Integrated Schedule.This will combine multiple independent plans into a single portfolio plan.This role will also be responsible for building new schedules for “must win” activities from capital to PPQ/Commercial supply.This role will involve working with the project manager, the SLT and a cross-functional site team as well as interacting with the GES Integration project team to ensure tight integration with that aspect of the project.
This is an opportunity for an experienced scheduler to gain further experience of the extended project lifecycle from start up to completion of PPQ batches on both the capital and client side of a strategic and high-profile biopharmaceutical project.
Requirements
Responsibilities:
* Drive creation of Site Portfolio Schedule (Microsoft Project)
* Transfer/Build the existing project schedules in Microsoft Project with connection to Primavera schedule where needed.
* Chair or assist with interactive scheduling workshops with various individuals and teams, within and outside of the site, to further develop the schedule.
* Maintain site portfolio schedule, alignment of sub project schedules, issuance of progress metrics (define and deliver).Support site governance in mitigation plan tracking.
* Develop a close working relationship with the scheduler on the capital project to identify critical common milestones and workload peaks and to ensure a tightly integrated schedule.
* Monitor progress and provide timely updates showing impact on milestones.
* Identify mitigations for impending delays and risks.
* Provide weekly updates to the project manager, leadership team and site project management office using established reporting tools.
Qualifications, Skills & Experience Required (Essential):
5 to 8 years working in a similar role in a pharmaceutical or preferably a biopharmaceutical environment with at least one major project involving implementation of MES and MBR.
Proficiency in Primavera scheduling tool.
Proficiency in Microsoft Project scheduling tool.
Proficiency as a user in Microsoft Excel, Powerpoint, Word, Outlook, Sharepoint.
Excellent interpersonal and communication skills, both written and verbal.
Desirable:
* Level 7 or 8 degree in a relevant scientific or technical discipline.
* Project Management Professional or similar qualification.
Skill-Set Expected:
* Ability to work on own initiative to resolve issues.
* Ability to multi-task and work to tight deadlines.
* Results and performance driven.
* Adaptable and flexible.
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Management and Manufacturing
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