Material Science Technical Specialist-Hybrid

Material Science Technical Specialist-Hybrid

• Industry Pharma/Biotech/Clinical Research
• Work Experience 4-5 years
• City Cork
• State/Province Cork
• Country Ireland

Job Description

About PSC Biotech

Who are we?

PSC Biotech is a leading Biotech Consultancy firm foundedin 1996, headquartered in Pomona, California, USA, with Global operations inIreland, India, Singapore, Australia and the US, serving 350 clients in morethan 23 countries worldwide. We provide cloud-based software solutions forQuality Management and Regulatory Inspections, pharmaceuticals contractmanufacturing professionals, and metrology services to our clients.

'Take your Career to a new Level'

PSC Biotech disrupts the conventional consultancy modelby aligning our EVP as one of the unique selling point which includes theopportunity to work with the most talented cohort of like-minded professionalsoperating in the Pharma/ Biotech Industry. We offer a permanent contract ofemployment giving exposure of working in Top Pharmaceutical client sites in adiverse-cultural work setting.

Employee Value Proposition

Employees are the "heartbeat" of PSC Biotech, we provideunparalleled empowering career development though Learning & Developmentin-house training mentorship through constant guidance to facilitate careerprogression. We believe in creating high performing teams that can exceed ourclient's expectations with regards to quality of all scalable and business unitdeliverables, staying under budget and ensuring timelines for our deliverablesare being met.

Overview:

Our client is seeking a Material Science TechnicalSpecialist to join the Global Process Services team. This is an excellentopportunity for an early-career professional with 3-5 years of experience inmaterial science, pharmaceutical manufacturing, biotechnology, or a relatedindustry.

The successful candidate will support material scienceactivities, technical supplier management, and GMP change control processeswhile collaborating with cross-functional teams in Ireland and the UnitedStates.

Requirements

Key Responsibilities:

• Support material science projects within the GlobalProcess Services team.
  
• Perform technical assessments of supplier changenotifications and material changes.
  
• Manage and support GMP change control activities relatedto raw materials and single-use technologies.
  
• Collaborate with suppliers to resolve technicalmaterial-related issues.
  
• Work closely with Procurement, Quality, Manufacturing,and Process Validation teams.
  
• Support the qualification, evaluation, and lifecyclemanagement of chemical raw materials and single-use technologies.
  
• Ensure compliance with GMP regulations, internal qualitystandards, and company procedures.
  
• Partner with global stakeholders to drive technicalsolutions and maintain supply continuity.
  
• Document technical assessments and maintain accuraterecords 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
  
• Change Control
  
• GMP-regulated environments
  
• Understanding of material qualification, suppliertechnical assessments, and quality systems.
  
• Strong analytical and problem-solving skills.
  
• Excellent written and verbal communication skills.
  
• Ability to work effectively within cross-functional andglobal teams.
  

Preferred Experience:

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

Working Model:

• Hybrid role based in Cork.
  
• Onsite attendance required Tuesday to Thursday.
  
• Work closely with a peer based in Cork and collaboratewith Process Validation teams and colleagues in the United States.