Medical Device Research jobs in Cork, County Cork
- PSC BiotechCork, County Cork
- 3–5 years of industry experience in pharmaceuticals, biotechnology, medical devices, or a GMP-regulated manufacturing environment.
- JacobsCork, County Cork
- You’ll play a key role in ensuring cost transparency, financial control, and commercial rigor across complex, multi disciplinary engineering programs.
- View all Jacobs jobs - Cork jobs - Cost Engineer jobs in Cork, County Cork
- Salary Search: Cost Engineer - Life Sciences salaries in Cork, County Cork
- See popular questions & answers about Jacobs
- QualcommCork, County Cork
- Employee stock purchase plan
- Bike to work scheme
- Experience with RTOS and modifying device drivers.
- The successful candidate will work on the development of software tools and user interfaces that support…
- QualcommCork, County Cork
- Employee stock purchase plan
- Bike to work scheme
- Support and manage global data collection campaigns involving Qualcomm staff, including hands‑on participation in field data collection using mobile and…
- AvantorCork, County Cork
- Experience supporting laboratory, pharmaceutical, biotechnology, or scientific research environments.
- Material Handler Coordinator / Inventory Management…
- MTD Precision EngineeringLittle Island, County Cork
- Flexitime
- Company pension
- On-site parking
Ad- Minimum of 1 years of experience in a design engineering role, preferably within the biopharmaceutical or medical device industries.
- Analog DevicesCork, County Cork
- Deep understanding of neural network quantization, pruning, knowledge distillation, and optimization techniques for resource-constrained devices.
- QualcommCork, County Cork
- Employee stock purchase plan
- Bike to work scheme
- Familiarity with enterprise deployment and device management concepts, such as Android Enterprise, mobile device management (MDM), and mobile application…
Senior Technical Product Manager
Often replies in 2 daysMalwarebytesCork, County Cork- Referral programme
- Comprehensive medical, dental, and vision insurance coverage.
- Strong technical background with experience working closely with engineering, security research,…
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View similar jobs with this employerAdvanced Energy Industries, Inc.Cork, County Cork- Ensure compliance with regulatory and safety standards for power solutions for medical devices.
- Translate research insights into practical prototypes and future…
- Advanced Energy Industries, Inc.Cork, County Cork
- Minimum 3+ years of experience in electronic design and development roles, preferably within medical devices or other high‑reliability systems.
- Advanced Energy Industries, Inc.Cork, County Cork
- Minimum 3+ years of experience in electronic design and development roles, preferably within medical devices or other high‑reliability systems.
- Advanced Energy Industries, Inc.Cork, County Cork
- Minimum 3+ years of experience in electronic design and development roles, preferably within medical devices or other high‑reliability systems.
Job Post Details
Material Science Technical Specialist-Hybrid - job post
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Job Description
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