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 clients 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 Manager Consultant is responsible to lead co-ordinate and deliver CAPEX project on-site at client location supporting and optimizing throughout.
Requirements
Requirements
Key Responsibilities:
Project Planning Execution & Monitoring
- Develop and execute project plans timelines budgets and resource allocations for large-scale biopharma CAPEX projects.
- Oversee the design construction and commissioning phases of biopharma facilitiesensuring alignment with project goals.
- Proactive drive Safety and Quality focus throughout project lifecycle.
- Track project milestones and ensure timely delivery of all phases.
- Prepare and present regular progress updates to senior management and stakeholders.
Stakeholder Management
- Act as the primary point of contact for internal teams contractors technical consultants and regulatory bodies.
- Ensure effective communication and collaboration between cross-functional teams including engineering procurement and quality assurance.
Budget and Financial
- Manage project budgets ensuring cost control and adherence to financial target.
- Prepare regular financial reports and forecasts for stakeholders and senior management.
Team Leadership
- Lead and motivate multidisciplinary teams ensuring alignment with project objectives.
- Mentor and provide guidance to team.
Regulatory Compliance
- Maintains company reputation by enforcing compliance with all relevant laws policies and regulations.
Risk Management
- Identify risks and implement mitigation strategies to ensure project success.
- Conduct regular risk assessments and update stakeholders on potential issues.
This is an onsite role.
Required Skills:
Experience in the Pharmaceutical GMP regulated industry desirable. Excellent verbal and written communication skills. Ability to work independently and as part of a team in a cross functional collaborative environment. Experience working with GMP Documentation Management Systems High level of attention to detail. Demonstrated ability to manage multiple priorities against ambitious timelines. Strong planning ability. Strong problem-solving skills and ability to work cross-functionally.
Required Education:
Trade qualification or 3rd level qualification in a relevant discipline or experience working and developing maintenance systems/CMMS.2 years or more experience working in a maintenance systems environment preferably in manufacturing GMP with a strong compliance / proficiency in document management systems and office applications. Knowledge and experience of CMMS systems ideally SAP & Procal.
About PSC Biotech Who are wePSC 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 solutio...
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 clients 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 Manager Consultant is responsible to lead co-ordinate and deliver CAPEX project on-site at client location supporting and optimizing throughout.
Requirements
Requirements
Key Responsibilities:
Project Planning Execution & Monitoring
- Develop and execute project plans timelines budgets and resource allocations for large-scale biopharma CAPEX projects.
- Oversee the design construction and commissioning phases of biopharma facilitiesensuring alignment with project goals.
- Proactive drive Safety and Quality focus throughout project lifecycle.
- Track project milestones and ensure timely delivery of all phases.
- Prepare and present regular progress updates to senior management and stakeholders.
Stakeholder Management
- Act as the primary point of contact for internal teams contractors technical consultants and regulatory bodies.
- Ensure effective communication and collaboration between cross-functional teams including engineering procurement and quality assurance.
Budget and Financial
- Manage project budgets ensuring cost control and adherence to financial target.
- Prepare regular financial reports and forecasts for stakeholders and senior management.
Team Leadership
- Lead and motivate multidisciplinary teams ensuring alignment with project objectives.
- Mentor and provide guidance to team.
Regulatory Compliance
- Maintains company reputation by enforcing compliance with all relevant laws policies and regulations.
Risk Management
- Identify risks and implement mitigation strategies to ensure project success.
- Conduct regular risk assessments and update stakeholders on potential issues.
This is an onsite role.
Required Skills:
Experience in the Pharmaceutical GMP regulated industry desirable. Excellent verbal and written communication skills. Ability to work independently and as part of a team in a cross functional collaborative environment. Experience working with GMP Documentation Management Systems High level of attention to detail. Demonstrated ability to manage multiple priorities against ambitious timelines. Strong planning ability. Strong problem-solving skills and ability to work cross-functionally.
Required Education:
Trade qualification or 3rd level qualification in a relevant discipline or experience working and developing maintenance systems/CMMS.2 years or more experience working in a maintenance systems environment preferably in manufacturing GMP with a strong compliance / proficiency in document management systems and office applications. Knowledge and experience of CMMS systems ideally SAP & Procal.
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