Johnson & Johnson

Manufacturing Quality Engineer I

Johnson & Johnson$65K — $104K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering or a related technical field
  • 0-2 years of relevant experience
  • Experience in Manufacturing/Operations
  • In-depth knowledge of product/process Risk Management (FDA and ISO standards)
  • Proven track record of risk mitigation implementation

Responsibilities

  • Provide quality engineering support for medical device development and manufacturing
  • Ensure compliance with quality system regulations in manufacturing processes
  • Lead quality reporting, including key performance metrics and objectives
  • Conduct activities related to the Material Review Board
  • Investigate non-conformances and implement corrective actions
  • Monitor production data to guide risk management and process improvement
  • Validate manufacturing processes and support equipment qualifications

Benefits

  • 401(k) and pension plan participation
  • 120 hours of vacation per year
  • 40-56 hours of sick time annually, depending on location
  • 13 days of holiday pay, including floating holidays
  • Up to 40 hours of Work, Personal, and Family Time per year
  • 480 hours of parental leave within one year of childbirth/adoption
  • Caregiver and bereavement leave policies
  • 32 hours of Volunteer Leave per year
Full Job Description

Job Function:

Supply Chain Engineering

Job Sub Function:

Quality Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Danvers, Massachusetts, United States of America

Job Description:

Job Description

At Abiomed, part of Johnson & Johnson, we are currently seeking a highly skilled and motivated individual to join our team as an Manufacturing Quality Engineer I, to be located in Danvers, MA.

An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.

In this role, you will have the unique opportunity to contribute to the manufacturing of life-saving medical devices. As part of our "Patients First!" culture, you will play a crucial role in ensuring the highest quality standards are met to save lives and recover hearts.


Responsibilities and Duties:
  • Provide quality engineering support in the development and manufacturing of new and existing medical devices.

  • Ensure compliance of manufacturing processes and areas to all applicable quality system regulations.

  • Lead Quality reporting such as, key performance metrics, goals, and objectives.

  • Lead and support activities related to the Material Review Board.

  • Lead non-conformance investigations, including cause analysis, documenting findings, and approving material dispositions. Promptly address any quality concerns through corrections, corrective/preventative actions, and Escalations.

  • Monitor and analyze production information to support risk management and provide direction for corrective and preventive actions (CAPA) and/or process improvement activities.

  • Validate manufacturing processes, including activities associated with equipment installation qualification (IQ), operational qualification (OQ), performance qualification (PQ), Test method validations (TMV).

  • Collaborate with manufacturing engineering to ensure the implementation of necessary process controls and validations, while adhering to established guidelines (GMP).

  • Support process optimization using design of experiments (DOE) and retrospective data analysis to understand and minimize sources of process variation affecting products. Identify key process input variables and key process output variables.

  • Support Quality Management System (process development, creating and editing new and existing SOPs). Support internal and external auditing requirements in manufacturing.


Qualifications:

Education:

  • A minimum of a Bachelor's degree, preferably in an Engineering field or related technical field  

Experience and Skills:

Required:

  • This position will require 0-2 years of relevant experience

  • Experience working in Manufacturing/Operations

  • In-depth knowledge of product/process Risk Management (FDA and ISO standards)

  • Experience with a proven track record of implementing appropriate risk mitigation

  • Good technical understanding of manufacturing equipment and processes

Preferred:

  • Experience working in both an FDA and European regulatory environment   

  • The ability to perform "hands on" troubleshooting and problem solving is preferred while quick thinking and sound judgment is highly desired  

  • A thorough understanding of GMP/ISO regulations and validation regulations

  • Demonstrated project management and project leadership abilities

Required Skills:

 

Preferred Skills:

Customer Centricity, Data Savvy, Document Management, Execution Focus, Good Automated Manufacturing Practice (GAMP), Issue Escalation, Lean Supply Chain Management, Process Control, Process Improvements, Quality Control Testing, Quality Services, Quality Standards, Quality Systems Documentation, Science, Technology, Engineering, and Math (STEM) Application, Supervision, Supply Planning, Technologically Savvy

 

 

The anticipated base pay range for this position is :

$65,000.00 - $104,650.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).

Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:

Vacation –120 hours per calendar year

Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year

Holiday pay, including Floating Holidays –13 days per calendar year

Work, Personal and Family Time - up to 40 hours per calendar year

Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child

Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year

Caregiver Leave – 80 hours in a 52-week rolling period10 days

Volunteer Leave – 32 hours per calendar year

Military Spouse Time-Off – 80 hours per calendar year

For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

Johnson & Johnson Careers

Joining Johnson & Johnson provides an unparalleled opportunity to be a part of a global team of professionals dedicated to blending care, science, and innovation to profoundly change the trajectory of health for humanity.

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At Johnson & Johnson, you will engage in work that matters. Join our community of professionals in health care to drive significant and impactful changes across the globe. Our team at Johnson & Johnson leads with science and heart in sectors from pharmaceuticals to medical devices and consumer health products.

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Leverage Johnson & Johnson’s culture of innovation to transform health care and improve the lives of people around the world. Our collaborative environment encourages leadership and growth, allowing you to pioneer new strategies for health care solutions with a diverse team of experts.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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