Supplier Quality Engineer III Job
Company Name:
Depuy Products Inc. (6030)
Raynham, MA, US
Supplier Quality Engineer III
Description
DePuy Synthes Companies is a member of Johnson & Johnson's Family of Companies, and is recruiting for a Supplier Quality Engineer III located in West Chester, PA or Raynham, MA.
DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological business in the world. DePuy Synthes Companies offer an unparalleled breadth and depth of products, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, craniomaxillofacial, power tools and biomaterials. Building on the legacy and strengths of two great companies, more agile and better equipped to meet the needs of today's evolving health care environment. With a focus on activating insights to develop innovative, comprehensive solutions, we are inspired to advance patient care in greater ways than either company could accomplish on its own.
The Supplier Quality Engineer III provides overall quality assurance leadership in the management of select contract manufacturing sites and raw material suppliers engaged in the production of Johnson and Johnson products. Responsibilities are defined below.
The Supplier Quality Engineer III will conduct audits to good manufacturing practices, international organization for standardization and any other applicable standards. He/she will provide complex product team support for quality system design and audit, compliance assessment, and for support of steady state manufacturing processes. This individual will utilize multifaceted industry and process excellence standards on an expert level in daily quality operations, including good manufacturing practices (GMP), equipment engineering system (EES), and international organization for standardization (ISO). The Supplier Quality Engineer III will address and correct product and process complaints. He/she will report on contract manufacturer performance metrics and management reviews. This individual will oversee audits of all quality system categories to assess compliance to process excellence standards. The Supplier Quality Engineer III will ensure comprehensive measurement systems to monitor effectiveness of quality and reliability systems to identify, bracket, correct and prevent defects, presenting reports to management. He/she will handle complex technical issues for manufacturing processes that are to be transferred to satellite facilities. This individual will provide Quality Engineering support to suppliers including audits/assessments, inspection technique support, verification/validation activities, CAPA and change management. FDA CFR Part 820 and ISO 13485 regulations/standards will be the focus.
Qualifications
A minimum of a Bachelor's Degree is required. A Degree in Engineering, Life Science, or related discipline is preferred. A minimum of 5 years of experience in a GMP and/or ISO regulated industry is required. Experience in the medical device and/or pharmaceutical industry is preferred. Operations supplier quality experience is preferred. Both, FDA and ISO regulations knowledge is required. FDA CFR Part 820 and/or ISO 13485 knowledge is preferred. Auditing background is preferred. Strong communication, teamwork, and problem solving skills are required. Strong root cause analysis skills are required. Experience or knowledge with machining manufacturing processes and injection molding is preferred. Six Sigma, Lean, or ASQ Certification and trainings are preferred.
This position will be based in West Chester, PA or Raynham, MA and require up to 25% travel, including possible international travel.
BE VITAL in your career, Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.
J2W: LI NA
J2W:BIO
J2W:NSJ
J2W:MZ
J2W:DICE
Primary Location:
North America-United States-Massachusetts-Raynham
Other Locations:
North America-United States-Pennsylvania-West Chester
Organization:
Depuy Products Inc. (6030)
Travel:
Yes, 25 % of the Time
Job Function:
Quality (Eng)
Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.
EEO is the Law
EEO is the Law GINA SupplementEstimated Salary: $20 to $28 per hour based on qualifications.
Depuy Products Inc. (6030)
Raynham, MA, US
Supplier Quality Engineer III
Description
DePuy Synthes Companies is a member of Johnson & Johnson's Family of Companies, and is recruiting for a Supplier Quality Engineer III located in West Chester, PA or Raynham, MA.
DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological business in the world. DePuy Synthes Companies offer an unparalleled breadth and depth of products, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, craniomaxillofacial, power tools and biomaterials. Building on the legacy and strengths of two great companies, more agile and better equipped to meet the needs of today's evolving health care environment. With a focus on activating insights to develop innovative, comprehensive solutions, we are inspired to advance patient care in greater ways than either company could accomplish on its own.
The Supplier Quality Engineer III provides overall quality assurance leadership in the management of select contract manufacturing sites and raw material suppliers engaged in the production of Johnson and Johnson products. Responsibilities are defined below.
The Supplier Quality Engineer III will conduct audits to good manufacturing practices, international organization for standardization and any other applicable standards. He/she will provide complex product team support for quality system design and audit, compliance assessment, and for support of steady state manufacturing processes. This individual will utilize multifaceted industry and process excellence standards on an expert level in daily quality operations, including good manufacturing practices (GMP), equipment engineering system (EES), and international organization for standardization (ISO). The Supplier Quality Engineer III will address and correct product and process complaints. He/she will report on contract manufacturer performance metrics and management reviews. This individual will oversee audits of all quality system categories to assess compliance to process excellence standards. The Supplier Quality Engineer III will ensure comprehensive measurement systems to monitor effectiveness of quality and reliability systems to identify, bracket, correct and prevent defects, presenting reports to management. He/she will handle complex technical issues for manufacturing processes that are to be transferred to satellite facilities. This individual will provide Quality Engineering support to suppliers including audits/assessments, inspection technique support, verification/validation activities, CAPA and change management. FDA CFR Part 820 and ISO 13485 regulations/standards will be the focus.
Qualifications
A minimum of a Bachelor's Degree is required. A Degree in Engineering, Life Science, or related discipline is preferred. A minimum of 5 years of experience in a GMP and/or ISO regulated industry is required. Experience in the medical device and/or pharmaceutical industry is preferred. Operations supplier quality experience is preferred. Both, FDA and ISO regulations knowledge is required. FDA CFR Part 820 and/or ISO 13485 knowledge is preferred. Auditing background is preferred. Strong communication, teamwork, and problem solving skills are required. Strong root cause analysis skills are required. Experience or knowledge with machining manufacturing processes and injection molding is preferred. Six Sigma, Lean, or ASQ Certification and trainings are preferred.
This position will be based in West Chester, PA or Raynham, MA and require up to 25% travel, including possible international travel.
BE VITAL in your career, Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.
J2W: LI NA
J2W:BIO
J2W:NSJ
J2W:MZ
J2W:DICE
Primary Location:
North America-United States-Massachusetts-Raynham
Other Locations:
North America-United States-Pennsylvania-West Chester
Organization:
Depuy Products Inc. (6030)
Travel:
Yes, 25 % of the Time
Job Function:
Quality (Eng)
Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status, or any other characteristic protected by law.
EEO is the Law
EEO is the Law GINA SupplementEstimated Salary: $20 to $28 per hour based on qualifications.
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