Senior Quality Engineer II - Integra LifeSciences
Boston, MA
About the Job
Changing lives. Building Careers.
Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
The Senior Quality Engineer II is responsible for providing quality and engineering support to the Operations and Quality departments. Designs equipment and floor layouts. Responsible for equipment and process improvement projects, supporting introduction of new processes or equipment into the facility. Leading investigational activities around non-conformances and CAPA's. Works collaboratively with Manufacturing, Engineering, Quality Assurance, and other functional experts to support all daily operational activities. Consults with management to resolve quality, production, and efficiency problems. Functions in conjunction with manager and functional experts on special department projects. Works with internal departments to ensure implementation, maintenance, and improvement of the quality management system.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Primary responsibilities are to:
+ Seasoned professional with complete and in-depth conceptual and practical knowledge in providing quality and engineering support decisions.
+ A Self-Starter that requires minimum supervision in the execution of primary responsibilities.
+ Utilizes complete and in-depth conceptual and practical knowledge in own job discipline and basic knowledge of related job disciplines.
+ Applies knowledge of job discipline's best practices to internal processes
+ Positions at this level are individual contributors that are also capable of leading cross functional Teams.
+ Writing & coordinating efforts for the development and implementation of new and updated Quality System procedures for ISO/QSR, such as validation protocols, manufacturing procedures, product & material specifications, design & development documentation, SOPs, development, and task force projects.
+ Leads multi disciplined Team in the development and execution of Process FMEA and other applicable risk analysis as deemed appropriate.
+ Oversees and participates in risk management processes, including the identification, evaluation, and mitigation of potential risks associated with product quality, safety, and regulatory compliance.
+ Develop, Collect, Analyze, and report Quality Metrics
+ Develop statistically based sampling plans for in-process and final testing and inspections, and validations.
+ Work with project teams to develop DOEs and statistically sound tests for appropriate support of results.
+ Develop, review and approve validations and completion reports for new and existing products, processes and equipment. Provide statistical analysis of the data to support the reports.
+ Ensure that all projects are compliant with GLP, QSR (including Design Controls), ISO or other applicable requirements.
+ Formulate detailed product quality plans based on results of risk analysis,
+ Support as required the Quality Management Review Process
+ Participate in FDA inspections, ISO Certification and surveillance audits and customer audits.
+ Support corporate Regulatory Affairs by providing information for submissions and Annual Reports.
+ Identify and implement opportunities for continuous improvement.
+ Audit internal groups or programs and external vendors for compliance with corporate and international regulatory guidelines.
+ Interact and coordinate activities with other departments, external vendors and customers.
+ Work with Product Development team in order to ensure all aspects of Design Transfer activities are being met
+ As required, assist or lead in the prompt implementation of Non-Conformance resolution.
+ Identifying and investigating quality issues, conducting root cause analysis, and implementing corrective and preventive actions (CAPAs) to address non-conformities and improve product quality.
+ Aid in the implementation SPC (Statistical Process Control) control systems with Manufacturing and Quality Control as applicable,
+ Provide Training assistance, including providing training in quality system activities/requirements, and mentoring/coaching of Junior Peers.
+ Perform other Quality Systems related duties as required.
+ Perform other duties as required.
+ On site position.
QUALIFICATIONS
+ Must have Bachelor's degree in Engineering, or Biological Sciences discipline with a minimum of 8+ years of directly related experience, advanced degree preferred
+ Minimum 3+ years experience in Quality Engineering in a regulated med device, life sciences or pharma industry.
+ Minimum 3+ years experience in dFMEA and pFMEA.
+ Minimum 3+ years experience with ISO 13485, ISO 14971, FDA QSR
+ Preferred 1 - 3 years' experience w/ SPC (Statistical Process Control)
+ Preferred 1 - 3 years' experience w/ MSA (Measurement Systems Analysis)
+ Versed in Design Controls
+ Probability & Statistics Working usage and knowledge of Probability & Statistics
+ Preferred professional certifications - CQE, CQA, CRE
+ Highly proficient in computer competence, including experience with database and Microsoft Office software to create reports, spreadsheets, analyze data and prepare presentations.
+ Able to support manufacturing by analyzing process data and recommending changes to improve quality.
+ Ability to query databases and generate reports.
+ Ability to follow instructions precisely, recognize deviations, and recommend corrective action.
+ Detail-oriented.
Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.
This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:
EEO Is the Law (https://www.eeoc.gov/laws/index.cfm) | EOE including Disability/Protected Veterans (https://www.eeoc.gov/eeoc/publications/ada_veterans_employers.cfm)
Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA (https://www.eeoc.gov/eeoc/publications/fs-ada.cfm) . If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com or call us at 855-936-2666.
Integra - Employer Branding from Integra LifeSciences on Vimeo (https://player.vimeo.com/video/265760526)
Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
The Senior Quality Engineer II is responsible for providing quality and engineering support to the Operations and Quality departments. Designs equipment and floor layouts. Responsible for equipment and process improvement projects, supporting introduction of new processes or equipment into the facility. Leading investigational activities around non-conformances and CAPA's. Works collaboratively with Manufacturing, Engineering, Quality Assurance, and other functional experts to support all daily operational activities. Consults with management to resolve quality, production, and efficiency problems. Functions in conjunction with manager and functional experts on special department projects. Works with internal departments to ensure implementation, maintenance, and improvement of the quality management system.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Primary responsibilities are to:
+ Seasoned professional with complete and in-depth conceptual and practical knowledge in providing quality and engineering support decisions.
+ A Self-Starter that requires minimum supervision in the execution of primary responsibilities.
+ Utilizes complete and in-depth conceptual and practical knowledge in own job discipline and basic knowledge of related job disciplines.
+ Applies knowledge of job discipline's best practices to internal processes
+ Positions at this level are individual contributors that are also capable of leading cross functional Teams.
+ Writing & coordinating efforts for the development and implementation of new and updated Quality System procedures for ISO/QSR, such as validation protocols, manufacturing procedures, product & material specifications, design & development documentation, SOPs, development, and task force projects.
+ Leads multi disciplined Team in the development and execution of Process FMEA and other applicable risk analysis as deemed appropriate.
+ Oversees and participates in risk management processes, including the identification, evaluation, and mitigation of potential risks associated with product quality, safety, and regulatory compliance.
+ Develop, Collect, Analyze, and report Quality Metrics
+ Develop statistically based sampling plans for in-process and final testing and inspections, and validations.
+ Work with project teams to develop DOEs and statistically sound tests for appropriate support of results.
+ Develop, review and approve validations and completion reports for new and existing products, processes and equipment. Provide statistical analysis of the data to support the reports.
+ Ensure that all projects are compliant with GLP, QSR (including Design Controls), ISO or other applicable requirements.
+ Formulate detailed product quality plans based on results of risk analysis,
+ Support as required the Quality Management Review Process
+ Participate in FDA inspections, ISO Certification and surveillance audits and customer audits.
+ Support corporate Regulatory Affairs by providing information for submissions and Annual Reports.
+ Identify and implement opportunities for continuous improvement.
+ Audit internal groups or programs and external vendors for compliance with corporate and international regulatory guidelines.
+ Interact and coordinate activities with other departments, external vendors and customers.
+ Work with Product Development team in order to ensure all aspects of Design Transfer activities are being met
+ As required, assist or lead in the prompt implementation of Non-Conformance resolution.
+ Identifying and investigating quality issues, conducting root cause analysis, and implementing corrective and preventive actions (CAPAs) to address non-conformities and improve product quality.
+ Aid in the implementation SPC (Statistical Process Control) control systems with Manufacturing and Quality Control as applicable,
+ Provide Training assistance, including providing training in quality system activities/requirements, and mentoring/coaching of Junior Peers.
+ Perform other Quality Systems related duties as required.
+ Perform other duties as required.
+ On site position.
QUALIFICATIONS
+ Must have Bachelor's degree in Engineering, or Biological Sciences discipline with a minimum of 8+ years of directly related experience, advanced degree preferred
+ Minimum 3+ years experience in Quality Engineering in a regulated med device, life sciences or pharma industry.
+ Minimum 3+ years experience in dFMEA and pFMEA.
+ Minimum 3+ years experience with ISO 13485, ISO 14971, FDA QSR
+ Preferred 1 - 3 years' experience w/ SPC (Statistical Process Control)
+ Preferred 1 - 3 years' experience w/ MSA (Measurement Systems Analysis)
+ Versed in Design Controls
+ Probability & Statistics Working usage and knowledge of Probability & Statistics
+ Preferred professional certifications - CQE, CQA, CRE
+ Highly proficient in computer competence, including experience with database and Microsoft Office software to create reports, spreadsheets, analyze data and prepare presentations.
+ Able to support manufacturing by analyzing process data and recommending changes to improve quality.
+ Ability to query databases and generate reports.
+ Ability to follow instructions precisely, recognize deviations, and recommend corrective action.
+ Detail-oriented.
Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.
This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:
EEO Is the Law (https://www.eeoc.gov/laws/index.cfm) | EOE including Disability/Protected Veterans (https://www.eeoc.gov/eeoc/publications/ada_veterans_employers.cfm)
Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA (https://www.eeoc.gov/eeoc/publications/fs-ada.cfm) . If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com or call us at 855-936-2666.
Integra - Employer Branding from Integra LifeSciences on Vimeo (https://player.vimeo.com/video/265760526)
Source : Integra LifeSciences
