Senior Supervisor, Manufacturing

Posted Yesterday
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Cartago, Cartago, CRI
In-Office
Senior level
Healthtech • Pharmaceutical
The Role
Supervise manufacturing personnel and production activities across multiple areas. Lead improvement projects, investigations, corrective actions, scheduling, staffing, training, quality and productivity tracking, documentation, and employee relations. Partner with engineering and cross-functional teams to achieve production targets and resolve performance issues. Own assembly procedures and project outcomes, mentor supervisors, and support management responsibilities when needed.
Summary Generated by Built In

Make a meaningful difference to patients around the world. At Edwards Lifesciences facilities around the world, our Manufacturing teams create the tools, technologies, and devices that transform patients’ lives. As part of our sewing, assembly, delivery, and distribution teams, your attention to detail and commitment to continuous improvement will help us turn innovative ideas into reality. Your purpose-driven work will help leave lasting and positive impacts on patient lives.


How you’ll make an impact:


  • Supervise employees and manufacturing activities pertaining to the production of products and/or manufacturing processes in - and with manufacturing/technical knowledge of - multiple production areas, depending on the complexity of the areas, to ensure the specifications and procedures of the company, in addition to conducting performance reviews, including resolving performance issues
  • Lead complex improvement projects, partner with engineering on investigations and/or corrective actions, perform non-conformance investigations for review with engineering, assures documentation content is valid including designing, implementing and optimizing procedures and working methods.
  • Establish the scheduling of work orders and team performance metrics, including monitoring output and adjusting schedules to ensure production targets are achieved
  • Accountable for productivity and quality metrics of staff, and provide regular progress reports and manufacturing metrics to management and cross-functional stakeholders, including developing resolutions as needed to improve metrics achievement
  • Ensure appropriate staffing for all positions
  • Accountable to ensure staff is appropriately trained to perform assigned work
  • Document owner for assigned product line assembly procedures
  • Responsible for all project outcomes of assigned unit/group of employees
  • May guide and mentor entry level supervisors
  • May provide management duties in the absence of Manager
  • Other incidental duties.

 

What you’ll need (Required):


  • Bachelor's degree in Industrial Engineering, Business Administration or related field.
  • More than 5 years of experience in personnel supervisory with full responsibility for all personnel and handling all aspects of employee relations. In addition, depth technical knowledge and experience in assigned work area, and substantial experience in related manufacturing, quality and/or product development engineering.
  • Experience working in manufacturing process, medical device industry or related industries.
  • Intermediate English level.
  • Availability to work in La Lima, Cartago
  • Availability to work in Shift A (Monday to Friday 6.00 a.m. to 3.30 p.m) or Shift B (Monday to Friday 2.25 p.m. to 10.25 p.m.)

What else we look for (preferred):


  • Proven expertise in Microsoft Office Suite with working knowledge of Enterprise Resource Planning (ERP) system
  • Excellent communication and interpersonal relationship skills; possessing strong collaboration skills in partnering with cross functional stakeholders in order to achieve objectives, as well as mediating differences to achieve consensus.
  • Knowledge of project management.
  • Knowledge of lean manufacturing tools.
  • Knowledge in applying process related to employee relations (disciplinary actions, layoffs, disciplinary investigations, performance improvements plans, performance evaluations)
  • Knowledge in quality systems related to CAPAs (corrective and preventive action) and NCRs (non-conformance report).

Skills Required

  • Bachelor's degree in Industrial Engineering, Business Administration, or a related field
  • More than 5 years of personnel supervision experience with responsibility for employee relations
  • Deep technical knowledge and experience in the assigned work area
  • Substantial experience in manufacturing, quality, or product development engineering
  • Experience with manufacturing processes, the medical device industry, or related industries
  • Intermediate English proficiency
  • Availability to work in La Lima, Cartago
  • Availability to work Shift A or Shift B
  • Expertise in Microsoft Office Suite and working knowledge of an ERP system
  • Excellent communication, interpersonal, collaboration, and conflict-mediation skills
  • Knowledge of project management
  • Knowledge of lean manufacturing tools
  • Knowledge of employee-relations processes, including disciplinary actions, layoffs, investigations, performance improvement plans, and evaluations
  • Knowledge of quality systems involving CAPAs and NCRs

Edwards Lifesciences Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Edwards Lifesciences and has not been reviewed or approved by Edwards Lifesciences.

  • Healthcare Strength — Health coverage is considered strong, with multiple plan choices, HSA options, and fertility support, and the company highlights holistic well‑being programs.
  • Retirement Support — A company 401(k) match and well‑regarded retirement offerings add clear long‑term value to total compensation.
  • Equity Value & Accessibility — An Employee Stock Purchase Plan with a discount and look‑back feature makes equity ownership accessible and enhances the total rewards package.

Edwards Lifesciences Insights

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The Company
HQ: Irvine, CA
13,687 Employees
Year Founded: 1958

What We Do

Edwards Lifesciences (NYSE: EW), is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. We thrive on discovery and expanding the boundaries of medical technology, serving patients in 100+ countries, with the help of our employees in areas including Clinical Affairs, Quality Engineering, Research & Development, Regulatory Affairs, Sales & Marketing, corporate functions and more. Our roots date back to 1958 when Miles Lowell Edwards, a retired engineer with a background in hydraulics and fuel pump operations, set out to build the first artificial heart. Edwards believed the heart could be mechanized and was encouraged by Dr. Albert Starr to focus on developing an artificial heart valve. After just two years, the first Starr-Edwards mitral valve was developed and successfully placed in a patient. This innovation spawned Edwards Laboratories. Miles’ fascination with healing the heart and helping patients with heart disease stemmed from his own experience with rheumatic fever as a teenager and continues to fuel our patient-first culture today. Today, we are as passionate about providing innovative solutions for people fighting cardiovascular disease as we have ever been. It's our Credo. It takes integrity, collaboration, innovation, and focus. We are leaders in the design and manufacture of tissue replacement heart valves and repair products as well as advanced hemodynamic monitoring. We partner with physicians to innovate products designed to help patients live longer, healthier, and more productive lives. Our work is both rewarding and a privilege. The importance of what we do defines our approach. We work together to create an environment where ideas can flourish and we provide our people with the resources, expertise and support to bring those ideas to life. For our legal terms and trademarks, please visit: https://www.edwards.com/legal/legal-terms

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