Senior Manufacturing Quality Engineer

Cherry Hill, NJ - USA

Monthly Salary: $ 79000 - 127650

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at

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:

At Abiomed part of Johnson & Johnson we are currently seeking a highly skilled and motivated individual to join our team as a Sr. Manufacturing Quality Engineer to support our capital products line (Automated Impella Controller). In this role you will have the unique opportunity to contribute to manufacturing 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.

This position will be located in Danvers MA.

Responsibilities and Duties:

Provide quality engineering support in the development and manufacturing of new and existing capital products
Ensure compliance of manufacturing processes and areas to all applicable quality system regulations
Lead Quality reporting such as key performance metrics goals and objectives for capital products
Lead and support activities related to the Material Review Board for capital products
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 for capital products
Update and maintain risks management files including PFMEA
Monitor and analyze production information to support risk management and provide direction for corrective and preventive actions (CAPA) and/or process improvement activities for capital products
Validate manufacturing processes including activities associated with equipment installation qualification (IQ) operational qualification (OQ) performance qualification (PQ) Test method validations (TMV) for capital products
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 for capital products

Qualifications:

Education:

A minimum of Bachelors or equivalent University degree is required with a focus in engineering or a related field preferred.

Experience in medical device industry working under FDA regulations (21 CFR part 820) ISO 13485 and EU MDR.
Experience with formal problem-solving methodologies and deductive skills.
Good understanding of FDA QSRs ISO13485 ISO14971.
6 years of experience in QA/QE in the medical device field.
Experienced in qualification of production equipment and validation of production processes.
Experience with handling non-conforming material and assemblies including root cause investigations
Highly preferred:
- Experience with manufacturing capital equipment that is software enabled. Equivalent experience in the manufacturing of similar products will also be considered.
- ASQ CQE certification is a plus
- Degree in Software or Electrical engineering is a plus
- ISO 13485 Internal audit (or lead Auditor) certificate is a plus.
- Experience working with electrical medical devices
- Understanding and experience with IEC 62304 software life cycle

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation external applicants please contact us via . internal employees contact AskGS to be directed to your accommodation resource.

Required Skills:

Preferred Skills:

The anticipated base pay range for this position is :

$79000.00 - $127650.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans employees are eligible to participate in the Companys 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: - Experience:

Senior IC