R&D Engineer

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 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.

Description:

Role: Research & Development Engineer

Job Summary:

• The R&D Engineer is responsible for developing and delivering complex acute is cheremic 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.

A minimum of 2 years experience in all stages of medical device design and development (including design 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:

This is an opportunity to work with a ground-breaking biomedical. We are passionate about our work; we play vital roles across a range of professional disciplines, and care deeply about our customers and communities. At ****, our culture enables dynamic and impactful careers.

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

We would love to hear from YOU, if you have the following essential requirements: Honours degree in Mechanical or Biomedical Engineering or equivalent. A minimum of 2 years experience in all stages of medical device design and development (including design 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: This is an opportunity to work with a ground-breaking biomedical. We are passionate about our work; we play vital roles across a range of professional disciplines, and care deeply about our customers and communities. At ****, our culture enables dynamic and impactful careers. 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