Detail-oriented process improvers. Critical thinkers who see opportunities to develop and optimize work processes – finding ways to simplify, standardize, and automate.
People who own their work and drive productivity, change, and outcomes.
Goal-oriented: Keeping the customer and requirements squarely focused, people who deliver safe and robust solutions.
Delivers results. A driven player who sets high goals for personal achievement and organizational success.
What you will do:
Support the design and development of solutions for legacy products (Sustenance Engineering) under the guidance of senior engineers/ Manager.
Execute projects by collaborating with cross-functional teams such as New Product Introduction (NPI) and Verification and Validation (V&V).
Contribute to value improvement and design optimization activities.
Gain knowledge of engineering systems, including software and hardware design cycles.
Participate in sustaining engineering activities for mechanical, electronic hardware, software, and system-level projects.
Support efforts to meet performance, reliability, cost, and manufacturability goals in product design.
Coordinate with suppliers and contractors to implement design changes.
What You Need:
Bachelors/Masters in Mechanical, Mechatronics Engineering or BioMedical
3-5 years of relevant work experience (Preferably in Medical Device Domine)
Preferred Qualifications (Strongly desired):
Understanding of the Medical Device Design control process and sustenance activities.
Basic understanding of Engineering principles and design practices.
Familiarity with change control processes (ECN/ECR) is desirable.
Familiarity with CAD tools such as Creo and SolidWorks is a plus.
Knowledge of FEA tools like Ansys is a strong advantage.
Knowledge of materials and manufacturing processes is a plus.
Strong communication skills in English, both written and verbal.
Willingness to learn and work collaboratively with cross-functional teams.
Proficiency in basic engineering tools and software is an advantage.
