Material Science Technical Specialist -Hybrid

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:

Our client is seeking a Material Science Technical
Specialist to join the Global Process Services team. This is an excellent
opportunity for an early -career professional with 3–5 years of experience in
material science, pharmaceutical manufacturing, biotechnology, or a related
industry.

The successful candidate will support material science
activities, technical supplier management, and GMP change control processes
while collaborating with cross -functional teams in Ireland and the United
States.

Requirements

Key Responsibilities:

• Support material science projects within the Global
  Process Services team.
  
• Perform technical assessments of supplier change
  notifications and material changes.
  
• Manage and support GMP change control activities related
  to raw materials and single -use technologies.
  
• Collaborate with suppliers to resolve technical
  material -related issues.
  
• Work closely with Procurement, Quality, Manufacturing,
  and Process Validation teams.
  
• Support the qualification, evaluation, and lifecycle
  management of chemical raw materials and single -use technologies.
  
• Ensure compliance with GMP regulations, internal quality
  standards, and company procedures.
  
• Partner with global stakeholders to drive technical
  solutions and maintain supply continuity.
  
• Document technical assessments and maintain accurate
  records in accordance with quality requirements.
  

Required Qualifications:

• Bachelor's degree in Material Science, Chemistry,
  Chemical Engineering, Life Sciences, or a related scientific discipline.
  
• 3–5 years of industry experience in pharmaceuticals,
  biotechnology, medical devices, or a GMP -regulated manufacturing environment.
  

Experience working with:

• Material Science
  
• Single -Use Technologies
  
• Chemical Raw Materials
  
• Technical Supplier Management
  
• Supplier Change Notifications
  
• Change Control
  
• GMP -regulated environments
  
• Understanding of material qualification, supplier
  technical assessments, and quality systems.
  
• Strong analytical and problem -solving skills.
  
• Excellent written and verbal communication skills.
  
• Ability to work effectively within cross -functional and
  global teams.
  

Preferred Experience:

• Experience supporting Process Validation activities.
  
• Exposure to supplier qualification and technical risk
  assessments.
  
• Knowledge of pharmaceutical manufacturing processes and
  quality management systems.
  

Working Model:

• Hybrid role based in Cork.
  
• Onsite attendance required Tuesday to Thursday.
  
• Work closely with a peer based in Cork and collaborate
  with Process Validation teams and colleagues in the United States.
  
• 23 -Month Fixed -Term Contract