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Product Engineering Manager

Camarillo, CA, USA

Job ID

7609

Job Type

Full Time

Workspace

On-Site

Industry

Life Sciences

Date Posted

December 24, 2024

Date of Expiry

January 14, 2025

About the Role

The Product Engineering Manager will be responsible for developing new products/systems and evaluating quality observations through defined processes to meet strategic and day-to-day objectives. It requires both attention to detail and process considerations in the execution of responsibilities.

Key Activities

  • The Product Engineering Manager will be responsible for developing new products/systems and evaluating quality observations through defined processes to meet strategic and day-to-day objectives. It requires both attention to detail and process considerations in the execution of responsibilities.·         Responsible for training the staff on engineering process requirements that pertain to their position.

  • Knowledge and experience with non-conformance, complaint investigation, and CAPA processes.

  • Enthusiasm for being a hands-on contributor in all aspects of job function.

  • Self-motivated, self-directing, strong attention to detail, and excellent time management skills.

  • Strong interpersonal and management skills with the ability to communicate verbally and in writing effectively.

  • Experience in smaller company environments is preferred where multi-tasking skills are essential.

  • Ability to travel to customer/vendor sites, tradeshows, and meetings.

Preferred Skills

  • Microsoft Office: Proficient in Microsoft Office. 

  • Communication Skills: Written, verbal, and presentation; ability to engage, inspire and influence people.

Education and Experience

  • A bachelor's degree in a mechanical or biomedical engineering with eight years of related industry experience in sustaining engineering or new product development of orthopedic implants.

  • Knowledge of and experience with US FDA and ISO 13485 regulations, especially the design and change control processes. Knowledge of quality/regulatory requirements of European MDD directives and MDR regulations beneficial.

  • Medical device product development experience is a MUST.

About Us

Finding a great opportunity that fosters growth, a great culture, and leadership opportunities can be difficult. Top Quality Recruitment (TQR) connects professionals with leadership opportunities across the Packaging, Food and Beverage, Medical Devices, and Biotechnology industries. With 50+ years of experience, we believe in one-to-one communication and finding the best candidate/employer match possible.    


TQR is an equal-opportunity employer that encourages diversity. We will consider all applications.    
   
Accommodation for applicants with disabilities is available upon request.    

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