Product Engineering Manager at Top Quality Recruitment (TQR) in Camarillo, California

Posted in Other about 18 hours ago.

Type: full-time





Job Description:

Employment Type: Full-time

Available Positions: 1

Location: On-Site

Application Deadline: January 14th, 2024

Summary

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.

Educations & 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.

Are you looking for your next opportunity? We can help.

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.

Are you looking to hire? Get started here: https://www.topqualityrecruitment.com/fill-a-position/

See hiring advice: https://www.topqualityrecruitment.com/blog/

See all available opportunities: https://www.topqualityrecruitment.com/jobs/

We thank all applicants for their interest and appreciate the time and effort involved; however, due to the large volume of resumes received only those candidates selected for an interview will be contacted. Please attached your resume to your application.

Job ID: 7609
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