Senior Technology Development Manager

At Terumo, we advance lifesaving medical technologies to benefit society. Are you eager to make a difference with us? Here, you’ll grow your expertise while staying true to your personal aspirations.  

Guided by our Japanese heritage, we act with respect, take ownership, and pursue continuous improvement. If you see yourself in our values, keep reading; this might be the opportunity you're looking for

Department Info

The Terumo Europe Pharmaceutical Solutions Division (PSD) develops patient-oriented parenteral delivery solutions for therapeutic performance and safety.

 

Globally trusted for quality and precision, the Pharmaceutical Solutions Division offers pharmaceutical and medical device manufacturers around the world comprehensive product design and development services.

 

We have decades of experience collaborating with pharmaceutical companies from the earliest phases of drug development to product commercialization to optimize critical aspects of parenteral drug delivery.

 

Innovation and creativity are central to our value proposition. Our expert teams lead the industry in developing and manufacturing advanced, high-performing infusion and injection technologies for all parenteral applications.

Job Summary

As Senior Technology Development Manager you'll provide pre-sale technical support in presentations and product demonstrations to our customers. This role will require close collaboration with our Engineering, Manufacturing, R&D and PSD Marketing teams. Together we ensure that we meet our customer needs, capture opportunities to improve our existing portfolio and develop new products.     

Job Responsibilities

1. Business Development

•    Build strong relationships with customers to showcase the company's capabilities, services, and products.
•    Offer technical knowledge and support from clinical development to market launch for both internal and external stakeholders.
•    Collaborate with various departments (Product Development, Marketing, Production, Engineering, Manufacturing, R&D, QA, QC, Regulatory) on scale-up, technology transfer, process validation and product support.
•    Stay updated on GMP regulatory compliance, especially for parental drug delivery, and ensure company policies are compliant. 
•    Contribute to business development strategies by evaluating product performance, identifying needs, monitoring competitors, and analyzing customer feedback.
•    Present case studies and research at international conferences.

2. Quality

•    Adhere to and train associates on Terumo Europe Quality system requirements and processes.
•    Coordinate and follow up on improvement processes (including CAPAs) with relevant departments.
•    Monitor progress in standardization work (ISO, EN, IEC) relevant to medical devices.

3. Customer Support

•    Support our engineering department (product and process) on the development and manufacturing of new applications. 
•    Support Account Managers with technical expertise.
•    Provide training on products, technology, or other needs.
•    Offer engineering support in the field 

4. Documentation

•    Prepare and review various types of technical documentation.
•    Coordinate and participate in ISO TC 76 and TC 84 as needed.
•    Conduct functionality testing.
•    Convert data into pitch packs.

5. General
•    Foster teamwork and build trusting and collaborative relationships. 
•    Focus on quality results and continuous improvement opportunities.
 

Profile Description

•    Master’s degree in Chemical or Biomedical engineering, pharmaceutical sciences, or related field required
•    More than 10 years of experience in pharmaceutical or medical device industry
•    Experience in a complex and international manufacturing environment
•    Dedicated to meet the expectations and requirements of internal and external stakeholders
•    Ability to manage multiple projects simultaneously respecting challenging timelines
•    Ability to deal with ambiguity and different business cultures
•    Excellent analytical and problem-solving skills 
•    Excellent planning, organizational, project management skills 
•    Strong technical business writing  
•    Fluent in English (written and spoken). Other languages are an asset
•    Excellent knowledge of Microsoft Word, Excel, PowerPoint, and Outlook  
•    Based in Belgium but internationally oriented, willing to travel globally as required (up to 50%) 

Offer

We are offering a unique opportunity to support the development of new parenteral drug delivery systems being