Manager, Manufacturing Engineering

Posted Yesterday
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Alajuela, Alajuela, CRI
In-Office
Senior level
Healthtech
The Role
Manage manufacturing engineering for catheter production: lead teams, ensure QMS and HSE compliance, drive continuous improvement, support new product transfers, design/purchase equipment, lead root-cause/corrective actions, and manage cross-functional collaboration.
Summary Generated by Built In

Job Description:

SUMMARY: This position oversees the development and implementation of manufacturing processes to maintain proper product functionality as well as cost efficiency. Ensures the engineering team and other manufacturing areas work together. The position is responsible for the development of equipment to aid in the manufacturing process. Reviews, evaluates and implements engineering changes and specification requirements.

SCHEDULE: Monday - Friday 8:00 am - 5:00 pm.

ESSENTIAL DUTIES AND RESPONSABILITIES include the following. Other duties may be assigned.

  • Resolves personnel problems by analyzing data, investigating issues, identifying solutions, recommending action.
  • Responsible for ensuring compliance with all company regulations, policies and procedures for the Quality System compliance.
  • Responsible for ensuring compliance with all company regulations, policies and procedures for Health, Safety and environment compliance.
  • Manage and direct the activities for the Manufacturing Engineering departments across multiple manufacturing areas.
  • Develop and retain a high performing team through effective hiring, coaching, performance management, and training.
  • Leads the root cause and corrective action process for quality issues across the catheter manufacturing. Works cooperatively with other departments to identify, contain, document, implement and communicate root cause and corrective actions for quality issues.
  • Identify manufacturing process and equipment improvement opportunities, implement solutions, and ensure benefits are realized and results effectively communicated.
  • Write / Review internal technical reports.
  • Collaborate with R&D efforts to support new product introductions and ensure new products are successfully transferred from prototype and scaleup to full scale manufacturing.
  • Lead lean and other continuous improvement programs to improve safety, quality, service and efficiency. Support 5s and Kaizen events throughout the organization.
  • Directly supports sourcing initiatives including product evaluation, manufacturing process documentation, knowledge transfer, and site visits as required.
  • Responsible for ensuring personal and company compliance with local and company regulations, policies and procedures for Health, Safety and Environmental compliance.
  • Responsible for the purchase or design of equipment that meets health, safety and environmental standards set by the company.
  • Responsible for performing design reviews and pre-validation assessments to ensure the safe and environmentally sound start-up of new processes
  • Other duties may be assigned to meet business needs.

SUPERVISORY RESPONSIBILITIES.

Have supervisory responsibilities: Yes

Leadership: Supervise/manage/direct the selection, training, development, appraisal and work assignments of personnel.

Supervises: Manufacturing Engineer I, II, III and Staff.

Supervision: General Direction: receive very general guidance with respect to overall objectives; work is usually quite independent of others; operate within division or department policy guidelines using independent judgment in achieving assigned objectives.

EDUCATION and/or EXPERIENCE:

  • Bachelor's degree in engineering is required, 7-8 years of experience in supervisory and leadership roles (required).

  • Knowledge in medical industry standards (required).

  • Good written and oral English communication skills (required).

  • Demonstrated capacity to lead multidisciplinary teams (required).

OTHER SKILLS and ABILITIES:  

  • Ability to work in a self-managed work team environment.

  • Ability to work different work schedules.

  • Proficient personal computer skills including electronic mail, record keeping, routine database activity, word processing, spreadsheet and graphics.

  • Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations.

  • Ability to write reports, business correspondence, and procedure manuals.

  • Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public.

  • Ability to work with mathematical concepts such as probability and statistical inference.

  • Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations.

  • Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.  

  • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.

MANUAL DEXTERITY: Manual dexterity sufficient to reach/handle items and work with the fingers.

VISION REQUIREMENTS: No special vision requirements

WORK SCHEDULE/HOURS: Monday – Saturday.

TRAVEL: Occasional.

ENVIRONMENTAL WORKING CONDITIONS: Well-lighted, heated and/or air-conditioned indoor office setting with adequate ventilation.

PHYSICAL DEMANDS: Sedentary physical activity performing non-strenuous daily activities of an administrative nature.

Other physical working conditions: Moderate noise.

Skills Required

  • Bachelor's degree in engineering
  • 7-8 years supervisory and leadership experience
  • Knowledge of medical industry standards
  • Good written and oral English communication skills
  • Demonstrated ability to lead multidisciplinary teams
  • Proficient PC skills (email, record keeping, databases, word processing, spreadsheets, graphics)
  • Experience with lean/5S/Kaizen and continuous improvement programs
  • Ability to perform statistical analysis and interpret data
  • Ability to write technical reports and procedure manuals
  • Manual dexterity sufficient to reach/handle items

Confluent Medical Technologies, Inc. Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Confluent Medical Technologies, Inc. and has not been reviewed or approved by Confluent Medical Technologies, Inc..

  • Healthcare Strength Benefits are considered solid, with medical, dental, and vision coverage described positively and HSA-eligible options supported by employer contributions. Feedback suggests core health coverage is a relative bright spot within the total package.
  • Retirement Support A 401(k) with company match is repeatedly highlighted as a positive element. Feedback suggests retirement provisions add meaningful value to total compensation.
  • Fair & Transparent Compensation Compensation is considered competitive in several engineering and managerial tracks, with role-specific pay bands viewed as strong in those paths. Feedback suggests certain professional roles receive competitive pay bands.

Confluent Medical Technologies, Inc. Insights

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The Company
HQ: Scottsdale, AZ
1,068 Employees
Year Founded: 1991

What We Do

Confluent Medical Technologies applies materials science to MedTech innovation. Confluent specializes in expert design and development of large-scale manufacturing specializing in interventional catheter-based devices and implants. Our key capabilities include Nitinol components and tubing, balloon and complex catheters, high-precision polymer tubing, and implantable textiles. We operate in 8 state-of-the-art facilities across the United States and Costa Rica and currently employ over 2,000 employees. Confluent has earned the confidence of leaders in the medical device community through a proven track record of innovation, engineering, and manufacturing.

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