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  • 3 weeks ago

jobs description

About PSC Biotech

Who we are
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 cloudbased 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 likeminded 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 diversecultural work setting.

Employee Value Proposition
Employees are the heartbeat of PSC Biotech we provide unparalleled empowering career development... though Learning & Development inhouse 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.

Description:

Role: Associate Research & Development Engineer

Job Summary:
• The Associate R&D Engineer is responsible for developing and delivering complex acute ischaemic stroke projects with significant technical challenges.
• Responsible for various aspects of the projects including process development design development implementation of new equipment/automation and new product introduction.

The responsibilities and the impact YOU will have:
• Generate device concepts within the project team to address product performance criteria.
• Develop test models for prototype performance evaluations.
• Build and test prototypes; analyse test data and interpret to identify optimal solutions to technical challenges.
• Create detailed component and finished device assembly drawings/specifications using SolidWorks.
• Identify and select product materials assembly methods and define process settings.
• Contribute to the project team to deliver key objectives meeting performance time and cost targets.
• Leverage and liaise with external vendors / resources to achieve project goals.
• Write procedures protocols specifications and reports.
• Understand physician (user) techniques and clinical needs (disease state) and assist in developing product training materials.
• Other duties as assigned or required.

Requirements

We would love to hear from YOU if you have the following essential requirements:
• Honours degree in Mechanical or Biomedical Engineering or equivalent.
• Approximately 12 months experience in a medical device design or manufacturing environment
• Design experience with SolidWorks prototyping testing.
• Design and technical ability based on a broad and deep knowledge of fundamental engineering principles.
• Data review and statistical methods skills (Minitab).
• High level of technical writing and reporting skills.
• Strong work ethic creative problem solving capable of working on own initiative.

Desirable:
• Results and deadline driven with an ability to handle multiple tasks and operate in a fastpaced environment.
• Excellent interpersonal skills and ability to work with people to achieve results.
• Highly motivated and an enthusiastic selfstarter with the ability to work under own initiative and as a team player.
• Specific experience on Medical Devices cardiovascular or neurovascular implants or instruments.

This is what awaits YOU:

Whether you re one of the people who already work here or you re considering joining the team we offer:
• An opportunity to be part of a global market leader.
• A dynamic and inspiring working environment.
• Opportunities to work on challenging projects and assignments.
• Possibilities for further personal and professional development/education.

#LIDM1

We would love to hear from YOU, if you have the following essential requirements: Honours degree in Mechanical or Biomedical Engineering or equivalent. Approximately 12 months experience in a medical device design or manufacturing environment Design experience with SolidWorks, prototyping, testing. Design and technical ability based on a broad and deep knowledge of fundamental engineering principles. Data review and statistical methods skills (Minitab). High level of technical writing and reporting skills. Strong work ethic, creative problem solving, capable of working on own initiative. Desirable: Results and deadline driven with an ability to handle multiple tasks and operate in a fast-paced environment. Excellent interpersonal skills and ability to work with people to achieve results. Highly motivated and an enthusiastic self-starter with the ability to work under own initiative and as a team player. Specific experience on Medical Devices, cardiovascular or neurovascular implants or instruments. This is what awaits YOU: Whether you re one of the people who already work here, or you re considering joining the team, we offer: An opportunity to be part of a global market leader. A dynamic and inspiring working environment. Opportunities to work on challenging projects and assignments. Possibilities for further personal and professional development/education. #LI-DM1
Galway Ireland

salary-criteria

Apply - RD Engineer Galway