Quality Engineer - Puerto Rico

As a ProMed employee, you will contribute to the manufacture of products that have a significant impact on people’s lives. Through honesty, integrity, and collaboration, we strive to be the very best as we hire the very best.

ProMed was founded in 1989 addressing an industry need for cleanroom manufacturing of silicone components, specifically those having a medical application. We treat every component and finished device as though it will be used by a beloved family member or friend. We are dedicated to our customers and to our employees while helping to improve the health and well-being of people around the world.

Working as one to help many.

QUALITY ENGINEER

The Quality Engineer serves as the lead quality representative of assigned product lines for new product development, day-to-day manufacturing support, non-conformance, and acts as the independent review function. The Quality Engineer supports additional processes such as Supplier Quality, Internal Audit, Corrective and Preventive Action Procedure for Good Manufacturing Practice (CAPA), etc., in order to effect operational efficiency and economy, the Quality Engineer ensures continuous production of parts consistent with established standards, and to meet the customer’s desired results. The Quality Engineer ensures ProMed’s brand, philosophy, systems, policies, and procedures are properly implemented and observed.

ESSENTIAL DUTIES & RESPONSIBILITIES

Position duties and responsibilities include, but are not limited to the following:

• Develops and/or revises standard operations and working practices;
  • Develops and conducts training sessions related to revised practices; and
  • Reviews documentation and records to ensure compliance;
• Be the voice of quality for daily manufacturing in assigned departments by partnering with Operations and Engineering and providing guidance on issues in line with external standards, internal standards, and best practices;
• Develops and maintains strong relationships with production leads and production personnel;
• Leads engineering investigations when production issues arise;
• Facilitates development and implementation of production processes and controls (i.e. qualification, process capability, sampling plans, validation, etc.);
• Analyzes statistical data and product specifications to evaluate current standards and achieve targeted quality and repeatability;
• Assists with investigation of product non-conformance/complaints, root cause analysis, monitoring/trending of process and product, escalation of identified issues, and implements corrective action as it pertains to customer complaints and internal non-conformance;
• Plans, drafts, and routes change requests as necessary;
• Identifies and/or resolves dimensional characterization methodology and inspection criteria;
• Evaluates and recommends process improvements;
• Qualifies/validates processes and/or equipment to meet customer and ProMed’s objectives;
• Identifies customer needs and new manufacturing capabilities to enable future growth;
• Creates and reviews Process Failure Mode and Effects Analysis (pFMEA)s for new projects and existing production lines;
  • Identifies actions to reduce or eliminate the chance of failure occurrence;
  • Identifies process variables that, if controlled, can reduce the occurrence or improve the detection of failure conditions;
• Executes data analysis and generates reports for new product development team and production projects;
• Reviews prints and provides recommendations based on Design for Manufacturing principles;
• Manages the execution and reports generation for Gage R&Rs (gage repeatability and reproducibility);
• Manages and executes component qualification, validation and equipment qualification;
• Supports new product development, as needed;
• Meets expectations of regular, reliable attendance;
• Other Duties As Needed:Any other duties and tasks as deemed necessary and appropriate.

Required:

• Engineering degree with medical device-related background and a minimum of 3-4 years’ experience in the field;
• Experience in the Medical/Cleanroom industry;
• Knowledge of medical device regulation (21 CFR 820), QMS Standard ISO 13485, risk management (ISO 14971);
• Proficiency in statistical, quality and continuous improvement methods and tools;
• Knowledge of Coordinate Measuring Machine (CMM) dimensional measuring equipment, pin gages, and calipers, as well as other equipment as required;
• Knowledge of Statistical Process Control (SPC), Minitab, SQC pack, design of Methodology and blueprint reading;
• Must have Intermediate knowledge of Microsoft Office products to include, Word, Excel, PowerPoint, Outlook, and Project;
• Commitment to continuous improvement company-wide;
• Excellent communication and interpersonal skills both written and verbal; professional, courteous and friendly personality; clearly conveys ideas and information and receives information effectively;
• Excellent organizational, problem-solving and time-sensitive skills;
• Ability to create positive working relationships with a diverse group of people including gender, ethnicity, age, and cultural and skill level differences;
• Ability to work independently with minimal supervision;
• Ability to establish priorities and meet deadlines.

Preferred:

• Professional certification (i.e. ASQ, Six Sigma, etc.) preferred.

ProMed does not discriminate in employment opportunities or practices on the basis of race, color, creed, religion, national origin, ancestry, age, sex, marital status, order of protection, disability, military status, sexual orientation, gender identity, pregnancy, public assistance, family status, unfavorable discharge from military service, genetic information or other segmenting factor protected by law, or local human rights commission activity.