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.
Position Overview
The CapEX Planner Scheduler is responsible for project planning and control of capital projects at the Industrial Operations and Product Supply (IOPS) Facility in Co. Limerick.
Requirements
Key Responsibilities
- Hold a strong interpersonal skillset ability to tailor communication based on the audience.
- Drive positive engagement and interaction with cross-functional groups for schedule development and forward planning.
- Creation and delivery of the EPS and WBS layouts to reflect EPCM commissioning qualification and SU of GMP production areas and systems.
- Ability to plan schedule track and control several small capital projects ongoing simultaneously.
- Develop level 3 4 5 detailed schedules and implement planning reporting and analytical tools in Primavera P6.
- Ability to level load and resource planned work-fronts.
- Contractor schedule analysis and ability to draft a detailed master schedule involving multiple schedule inputs for larger capital projects.
- Experience in Critical Path Method planning & forecasting.
- Creation and maintenance of the Project Risk Register.
- Chairing weekly planning & scheduling focused meetings inclusive of roundtable workshop planning.
- Highlight schedule issues and constraints and propose potential mitigations.
- Ability to track and control and report out accurately plan vs actual via earned valve analysis s-curves histograms and tailored graphical updates as requested by management PowerPoint concise & snappy reporting.
- Establish KPIs and routinely track and report for the specific function you are working in.
- Comply with all current IOPS cGxPs (e.g. Good Manufacturing Processes Good Documentation Practices etc.).
- Lead by example. Share knowledge and experience within your team operate with a one IOPS mindset.
- May maintain the physical condition and environment of all areas and equipment. Maintain Safe Clean and Compliant (SCC) standards.
- Adhere to and remain current in assigned IOPS plant and department SOPs and required trainings as related to positional and department responsibilities; maintain an up-to-date training file to ensure compliance.
- Any other projects as assigned by supervisor.
Qualifications and Experience
- BS/BA in engineering or scientific related field or relevant trade qualification along with 5 years of experience in a similar position. May substitute relevant experience in lieu of educational requirement.
- Proficient knowledge & use of Oracle Primavera
- Proficient knowledge & use with the Microsoft Suite of Software Packages inclusive of MS Project
Required Skills:
Qualifications In order to excel in this role you will more than likely have: 1 to 2 years relevant experience. Experience and critical skills in the area of expertise that add value to the business; ideally analytical microbiology in a GMP setting. Knowledge of cGMP. Report standards policy writing skills required. Lean Six Sigma Methodology experience. Understand the specific responsibilities of all departments as they relate to ones own department understanding the business processes ones department supports. Effective communication presentation and interpersonal skills to interface effectively with all levels of colleagues and with external customers in a team orientated manner. Third Level science qualification (Microbiology is preferred).
Required Education:
Qualifications and ExperienceBachelors degree in Engineering Science Construction Management or a related discipline (or equivalent relevant experience).Minimum 5 years of experience in project planning scheduling or project coordination ideally within a GMP-regulated pharmaceutical or manufacturing in Microsoft Project and Microsoft Office with Primavera P6 or other enterprise scheduling tools is highly analytical and organ
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.
Position Overview
The CapEX Planner Scheduler is responsible for project planning and control of capital projects at the Industrial Operations and Product Supply (IOPS) Facility in Co. Limerick.
Requirements
Key Responsibilities
- Hold a strong interpersonal skillset ability to tailor communication based on the audience.
- Drive positive engagement and interaction with cross-functional groups for schedule development and forward planning.
- Creation and delivery of the EPS and WBS layouts to reflect EPCM commissioning qualification and SU of GMP production areas and systems.
- Ability to plan schedule track and control several small capital projects ongoing simultaneously.
- Develop level 3 4 5 detailed schedules and implement planning reporting and analytical tools in Primavera P6.
- Ability to level load and resource planned work-fronts.
- Contractor schedule analysis and ability to draft a detailed master schedule involving multiple schedule inputs for larger capital projects.
- Experience in Critical Path Method planning & forecasting.
- Creation and maintenance of the Project Risk Register.
- Chairing weekly planning & scheduling focused meetings inclusive of roundtable workshop planning.
- Highlight schedule issues and constraints and propose potential mitigations.
- Ability to track and control and report out accurately plan vs actual via earned valve analysis s-curves histograms and tailored graphical updates as requested by management PowerPoint concise & snappy reporting.
- Establish KPIs and routinely track and report for the specific function you are working in.
- Comply with all current IOPS cGxPs (e.g. Good Manufacturing Processes Good Documentation Practices etc.).
- Lead by example. Share knowledge and experience within your team operate with a one IOPS mindset.
- May maintain the physical condition and environment of all areas and equipment. Maintain Safe Clean and Compliant (SCC) standards.
- Adhere to and remain current in assigned IOPS plant and department SOPs and required trainings as related to positional and department responsibilities; maintain an up-to-date training file to ensure compliance.
- Any other projects as assigned by supervisor.
Qualifications and Experience
- BS/BA in engineering or scientific related field or relevant trade qualification along with 5 years of experience in a similar position. May substitute relevant experience in lieu of educational requirement.
- Proficient knowledge & use of Oracle Primavera
- Proficient knowledge & use with the Microsoft Suite of Software Packages inclusive of MS Project
Required Skills:
Qualifications In order to excel in this role you will more than likely have: 1 to 2 years relevant experience. Experience and critical skills in the area of expertise that add value to the business; ideally analytical microbiology in a GMP setting. Knowledge of cGMP. Report standards policy writing skills required. Lean Six Sigma Methodology experience. Understand the specific responsibilities of all departments as they relate to ones own department understanding the business processes ones department supports. Effective communication presentation and interpersonal skills to interface effectively with all levels of colleagues and with external customers in a team orientated manner. Third Level science qualification (Microbiology is preferred).
Required Education:
Qualifications and ExperienceBachelors degree in Engineering Science Construction Management or a related discipline (or equivalent relevant experience).Minimum 5 years of experience in project planning scheduling or project coordination ideally within a GMP-regulated pharmaceutical or manufacturing in Microsoft Project and Microsoft Office with Primavera P6 or other enterprise scheduling tools is highly analytical and organ
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Posted on:
22-10-2025
Vacancies:
1 Vacancy
