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Sr Staff Engr, Product Development

In Massachusetts / United States

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Sr Staff Engr, Product Development   

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JOB TITLE:
Sr Staff Engr, Product Development
JOB TYPE:

JOB SKILLS:
JOB LOCATION:
Woburn Massachusetts / United States

JOB DESCRIPTION :
Sr. Quality Engineer, Sr. MFG
Pay Rate $109.45

On-site position - candidates submitted need to be within commuting distance to the site.

Must Have's:
Experience @ MFG Facility
Worked with MFG Operations (Operations Interface)
Experience with Class 3 Devices

Summary/Purpose of Position

Seeking a Sr Quality Engineer or Sr Mfg Engineer with Medical Device experience (Class III preferred), strong compliance background, that has worked at a manufacturing site and is familiar with Quality and Operations remediation. Depth of experience with CAPAs, root cause analysis, problem solving, development of permanent/systemic solutions, and implementation execution are all critical for this role.

Essential Duties and Position Responsibilities

-Core Responsibilities will be focused on small to medium sized QMS and Operational SOP remediation projects, including various subsystems of the Quality Management System and Production/Environment/Facility control mechanisms.

-Will be responsible to solve problems and implement solutions in the active quality/production environment – this includes troubleshooting with affected cross functional teams, execution through the change control process (MasterControl), and implementation of the updated documentation in the quality/production environment where there is Work in Process (WIP). Development of solutions and execution of the proposed changes are both critical elements of this position.

-Execution of CAPA investigations and implementation of CAPA action plans, along with tracking and completing verifications of CAPA effectiveness will be required as well.

-A self-starter, active, and hands-on person is needed for this role that will need to complete tasks and deliverables with minimal oversight. Strong engineering background is required, along with depth of experience with Medical Device manufacturing and compliance to regulatory standards (Class III Medical Device experience preferred).

Qualifications, Knowledge, and Skills Required:

-Engineering BS Degree with minimum of 5 years relevant working experience in Medical Device Industry.

-Extensive knowledge of engineering and scientific principles, concepts, and application.

-Demonstrated strong initiative and follow through in executing responsibilities, overcoming

obstacles and balancing multiple priorities effectively through strong technical and/or

leadership experience.

-Demonstrated and continuous track record of contributing to technical assignments with command and leadership, specifically for quality and manufacturing issue resolution and remediation.

-Strong background and extensive experience with completing content/documentation and implementing changes for CAPAs

-Experience with chemical/analytical testing and manufacturing/controlled environment monitoring testing

-Excellent organizational skills

-Excellent verbal and written communication skills.

-Experience with MasterControl (EDMS) and JDE (ERP) preferred

Examples of Areas/Processes requiring remediation activity:

Nonconforming material – Scrap process and interface with ERP system (JDE), Out of Specification process (Chemistry and Microbiology testing), Controlled Environment specifications and documentation/approvals for excursions, Equipment cleaning, Equipment repairs (unscheduled), Line clearance, Controlled temperature storage, GDP, Production Controls, Laboratory Controls, Shipping and Receiving, Warehouse and FG storage, Environmental Monitoring, Purified Water System, Lot Release, Approved Supplier List, Manufacturing Environment Cleaning

Position Details

Jun 16, 2021
S16204860793254452
Massachusetts / United States
Woburn
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Sr Staff Engr, Product Development    Apply

Click on the below icons to share this job to Linkedin, Twitter!

Sr. Quality Engineer, Sr. MFG
Pay Rate $109.45

On-site position - candidates submitted need to be within commuting distance to the site.

Must Have's:
Experience @ MFG Facility
Worked with MFG Operations (Operations Interface)
Experience with Class 3 Devices

Summary/Purpose of Position

Seeking a Sr Quality Engineer or Sr Mfg Engineer with Medical Device experience (Class III preferred), strong compliance background, that has worked at a manufacturing site and is familiar with Quality and Operations remediation. Depth of experience with CAPAs, root cause analysis, problem solving, development of permanent/systemic solutions, and implementation execution are all critical for this role.

Essential Duties and Position Responsibilities

-Core Responsibilities will be focused on small to medium sized QMS and Operational SOP remediation projects, including various subsystems of the Quality Management System and Production/Environment/Facility control mechanisms.

-Will be responsible to solve problems and implement solutions in the active quality/production environment – this includes troubleshooting with affected cross functional teams, execution through the change control process (MasterControl), and implementation of the updated documentation in the quality/production environment where there is Work in Process (WIP). Development of solutions and execution of the proposed changes are both critical elements of this position.

-Execution of CAPA investigations and implementation of CAPA action plans, along with tracking and completing verifications of CAPA effectiveness will be required as well.

-A self-starter, active, and hands-on person is needed for this role that will need to complete tasks and deliverables with minimal oversight. Strong engineering background is required, along with depth of experience with Medical Device manufacturing and compliance to regulatory standards (Class III Medical Device experience preferred).

Qualifications, Knowledge, and Skills Required:

-Engineering BS Degree with minimum of 5 years relevant working experience in Medical Device Industry.

-Extensive knowledge of engineering and scientific principles, concepts, and application.

-Demonstrated strong initiative and follow through in executing responsibilities, overcoming

obstacles and balancing multiple priorities effectively through strong technical and/or

leadership experience.

-Demonstrated and continuous track record of contributing to technical assignments with command and leadership, specifically for quality and manufacturing issue resolution and remediation.

-Strong background and extensive experience with completing content/documentation and implementing changes for CAPAs

-Experience with chemical/analytical testing and manufacturing/controlled environment monitoring testing

-Excellent organizational skills

-Excellent verbal and written communication skills.

-Experience with MasterControl (EDMS) and JDE (ERP) preferred

Examples of Areas/Processes requiring remediation activity:

Nonconforming material – Scrap process and interface with ERP system (JDE), Out of Specification process (Chemistry and Microbiology testing), Controlled Environment specifications and documentation/approvals for excursions, Equipment cleaning, Equipment repairs (unscheduled), Line clearance, Controlled temperature storage, GDP, Production Controls, Laboratory Controls, Shipping and Receiving, Warehouse and FG storage, Environmental Monitoring, Purified Water System, Lot Release, Approved Supplier List, Manufacturing Environment Cleaning