Employment Requirements
This opportunity is not open to C2C relationships or visa sponsorship.

This is opportunity is for local candidates only.

Responsibilities
Participates in efforts to define optimized processes and identify technical challenges based on data.
Identify suggestions to improve work processes.
Supports assigned projects; utilizes thorough technical and theoretical understanding of numerous manufacturing techniques.
Analyzes data, evaluates results, forms conclusions and provides/implements process or document improvements.
Applies advanced engineering knowledge to projects on manufacturability of designs aligned with supplier’s capability.
Executes experiments to optimize manufacturing processes / controls.
Utilizes DOE where appropriate.
Participates in technical team activities.
Shares knowledge and expertise with others.
Participates in project planning, process updates and contributes to experimental design.
Prepares and delivers presentations of project results to own or other groups.
Monitors work to ensure quality, and continuously promote Quality First Time.


Qualifications
Must have the ability to manage priorities based on the needs of the manufacturing area with some guidance from the reporting manager and senior management.
Knowledge of biomedical/biotechnology manufacturing.
Demonstrates potential for technical proficiency, engineering creativity, collaboration with others, and independent thought.
Strong understanding of engineering principles and concepts.
Strong computing skills utilizing Microsoft Office tools such as Excel, Word, and Powerpoint
Strong teamwork skills.
Demonstrated troubleshooting and problem solving skills including the use of designed experiments.
Ability to meet project deadlines.
Ability to multitask and prioritize with some guidance from management.
Automation & Factory Support specifics:
o Experience with automated manufacturing equipment and automation technologies.
o Experience with CAD programs such as Pro/Engineer and/or SolidWorks.
o Experience in a regulated environment. Knowledge of FDA Quality System Regulations (QSR’s) is a plus.
o Experience with Lean Systems.
Quality Support specifics:
o Experience in reagent or instrument manufacturing for a Medical Device or Pharmaceutical company.
o Experience in a regulated environment. Knowledge of FDA Quality System Regulations (QSRs).

Education and Experience
Bachelors of Science in ME or EE plus 4 years of experience
or
MS in ME or EE plus 2 years of experience


*Solü Technology Partners provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, national origin, age, disability or genetics.