EMPLOYMENT If you are looking for a position and would like to place a short ad (approx. 250 characters), please contact:

Eleanor Chilson 954-661-5197

This service is free to members of ASQ Section 1510.   Any South Florida area business with an opening for a quality related position may also place an announcement.  This is not limited to space (subject to availability) and you do not have to be a member. Ads for individuals seeking positions are free to ASQ Section 1510 / 1515 members and subject to space availability.  Ads for open positions in a quality related field are free and not limited to ASQ members. To place an ad, contact Eleanor Chilson.




Position: Quality Supervisor search, Mgr path, Innovative, $100k- $110k, Charlotte, NC     Posted 3/19/2019


I am seeking recommendations for a Quality Engineer ready to step into a leadership role.

Why this is a great opportunity:
- Large company with significant career options including international
- Recognized for product innovation
- Stable, excellent brand name, market leader
- Path to Quality Manager, prior supervision experience not required

What a candidate should bring:
- Knowledge of ISO-9001. 2015 highly preferred. Experience with additional QMS’ a plus
- Mechanical, electronic, or electro-mechanical product environment experience a plus
- SPC, 8D, CAR, NCR, FMEA - body of knowledge typical for a manufacturing Quality Engineer
- Some Lean tools would be good: 5S, Kaizen, etc
- BS


David W. Cole

FPC Vinings
4480 South Cobb Drive
Ste H #349
Smyrna, GA 30080
404-502-6784 <<<< current searches

David Cole
President at FPC Vinings, 404-502-6784 / - Operations Professional, Engineer, #1 Recruiter


Position: Senior Quality Engineer (Pompano Beach,FL)       Posted 11/15/2018

Company: Ortho Clinical Diagnostics

Ortho Clinical Diagnostics (Ortho) is a global leader of in vitro diagnostics.  Ortho serves two primary industries in the medical field: clinical laboratories, by producing platforms and assays that test for a variety of diseases, conditions, and substances; and immunohematology, by providing the means to ensure blood transfusion recipients receive appropriate and compatible blood.  

We are seeking a Senior Quality Engineer in Pompano Beach, FL: to provide manufacturing and software quality engineering expertise of product manufacture, raw material quality, validation, product related projects and investigations in a biological product manufacturing facility.  This position is also responsible for approval and review of manufacturing non-conformances while keeping into perspective the safety and efficacy of the products and business impact.  

The ideal candidate will have a Bachelor’s degree with a minimum of 7 years of experience at a regulated medical or manufacturing facility, or equivalent combination of education and experience. Background/experience with application of software quality engineering principles in biological product manufacturing is highly desirable.  A background in validation, statistical process controls, regulatory compliance, and knowledge of current and applicable GMP regulations and ISO standards is required. For full details, please visit our career site at


Position: Process Improvement Lead I         POSTED 9/6/2018

Location: Weston, Florida, US, 33331

Company: Teva Pharmaceutical Industries Ltd.

Company Info

Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.  Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation.  This is how we improve health and enable people to live better, healthier lives.  Join us on our journey of growth!

Job Description

Summary: Under limited supervision, responsible for establishing, leading and executing assigned continuous process improvement initiatives, acting as a liaison between operational and technical teams to identify, analyze and translate business needs into high quality process improvement solutions. Assists with establishing business cases and ROIs, consulting with the business in order to propose recommendations for senior management approval.

Essential Job Function: 

  • Participates on cross-functional teams tasked with solving business issues which require operational and/or technical solution providing subject matter insight with regards to operational process, policies/regulatory changes, and/or system functionality.
  • Analyzes, documents and maps operational processes through workflows. Capture pertinent process step details so that opportunities for process improvements, benchmarks, key performance indicators, current metrics, and target objectives can be defined.
  • Utilizes Six Sigma / DMAIC and related techniques to define improvement opportunities where deemed appropriate.
  • Contributes in strategic meetings to review, evaluate, and/or propose new business opportunities through the implementation/enhancement of operational and/or technical solutions, which are intended to improve customer relationships and operating efficiencies while reducing costs.
  • Creates and drives improvement plans to completion.
  • Develops, maintains, and provides process expertise in order to deliver knowledge transfer to cross-functional operational and technical areas for skill development.
  • Carries out responsibilities according to the organization’s policies and procedures, best practices, as well as in accordance with state, federal, and local laws, including applicable safety rules and regulations.
  • Performs other duties as assigned by Management.


Minimum Qualifications: Bachelor’s degree in Industrial Engineering or related field from an accredited college or university, and two (2) to five (5) years in Continuous Process Improvement and Data Analysis experience.

Physical Requirements and Working Conditions: Incumbents in this class are subject to extended periods of sitting, standing and walking, vision to monitor, moderate noise levels. Work is performed in an office environment.

Required Knowledge and Skills:

  • Process reengineering lifecycle methodologies and documentation.
  • Six sigma/DMAIC and/or continuous process improvement methodologies.
  • Project Management skills highly desired.
  • English usage, spelling, grammar and punctuation.

Skill in:

  • Evaluating and analyzing business needs to research problems’ root cause and to identify improvement opportunities based on data driven analysis.
  • Developing and executing process improvement plans.
  • Being able to influence without authority; interfacing professionally and effectively with all levels of personnel.
  • Establishing and maintaining cooperative working relationships with cross-functional teams.
  • Communicating clearly and concisely, both orally and in writing.
  • Complies with company policies, practices and procedures, including safety rules and regulation. Ability to work independently.
  • Handling multiple duties and assignments.


Project Management

Sub Function

CI / Black Belt / Six Sigma Process

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