Manufacturing Engineer II - eTeam Inc.
Mansfield, MA 02048
About the Job
Job Title: Manufacturing Engineer II
Location: Mansfield, MA 02048
Duration: 06 Months
Pay Range: $40.00 to $55.19
Responsibilities:
Understand and be knowledgeable of Equipment and Process Operations completed in the facility. This includes, site SOPs, Equipment documentation, capacity, setup, operation, disassembly, maintenance, cleaning, troubleshooting, monitoring, and programming of manufacturing equipment and facility.
Perform testing and troubleshooting on equipment to determine functionality level and capacity.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Create, update, and maintain equipment service work instructions.
Organize and write validation protocols associated with the manufacturing process.
Lead and support troubleshooting activities to minimize process downtime or re-occurrence.
Identify key process indicators and collect data to drive manufacturing and yield improvements.
Generation and execution of validation plans, validation protocols (IQ/OQ/PQ), and completion reports, with a major focus on sterilization and microbiology of medical devices.
Provide statistical analysis of the date to support the reports.
Generation and implementation of change controls and engineering notices (ECO).
Develop statistically based sampling plans for in-process and final testing and inspections, and validations. Troubleshooting equipment/processes that do not perform as intended during validation runs.
Recommend process/quality improvements as part of validation runs.
Evaluate, investigate, and document non-conformances incidents and/or protocol deviations.
Complete assigned Non-Conformance and CAPA investigations and prepare investigation reports. Develops and maintains an effective cross-functional working relationship with plant and corporate Manufacturing, Engineering, Regulatory, and Quality Assurance personnel.
Work on project teams with other internal departments, external vendors, and customers as required. Assure that existing processes and assigned activities fully comply with regulatory and/or international agencies, such as FDA, ISO, OSHA, EPA, among others.
Participate in the compilation and review of technical documentation for both domestic and international regulatory submissions.
Participate in external audits such as: FDA, Notified Body (BSI), and Corporate, among others.
Performs other related duties as necessary.
Qualifications:
BS in Engineering, preferably Mechanical, Industrial, Electrical, Chemical, or Biomedical (Professional Engineer License.) or science-related field.
Minimum of 4-6 years of experience in the medical device and/or pharmaceutical manufacturing environment.
Lean/Six Sigma . or Black Belt Certification is a plus.
Experience in validations such as manufacturing equipment, manufacturing processes, stability or aging, is required.
Knowledge of FDA, OSHA, EPA, and GMP's and ISO requirements.
Knowledge in Organizational Excellence and Lean/Six Sigma.
Strong Project Management skills.
Ability to lead teams through complex projects and provide departmental technical leadership.
Must have excellent communication skills and a strong track record of working cross-functionally.
Must have demonstrated ability to think strategically. Able to develop technical documentation such as: Change Controls, Validation Plans, Validation Protocols, Technical/investigation reports, SOP, and others. Teamwork-oriented and self-starter.
Location: Mansfield, MA 02048
Duration: 06 Months
Pay Range: $40.00 to $55.19
Responsibilities:
Understand and be knowledgeable of Equipment and Process Operations completed in the facility. This includes, site SOPs, Equipment documentation, capacity, setup, operation, disassembly, maintenance, cleaning, troubleshooting, monitoring, and programming of manufacturing equipment and facility.
Perform testing and troubleshooting on equipment to determine functionality level and capacity.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Create, update, and maintain equipment service work instructions.
Organize and write validation protocols associated with the manufacturing process.
Lead and support troubleshooting activities to minimize process downtime or re-occurrence.
Identify key process indicators and collect data to drive manufacturing and yield improvements.
Generation and execution of validation plans, validation protocols (IQ/OQ/PQ), and completion reports, with a major focus on sterilization and microbiology of medical devices.
Provide statistical analysis of the date to support the reports.
Generation and implementation of change controls and engineering notices (ECO).
Develop statistically based sampling plans for in-process and final testing and inspections, and validations. Troubleshooting equipment/processes that do not perform as intended during validation runs.
Recommend process/quality improvements as part of validation runs.
Evaluate, investigate, and document non-conformances incidents and/or protocol deviations.
Complete assigned Non-Conformance and CAPA investigations and prepare investigation reports. Develops and maintains an effective cross-functional working relationship with plant and corporate Manufacturing, Engineering, Regulatory, and Quality Assurance personnel.
Work on project teams with other internal departments, external vendors, and customers as required. Assure that existing processes and assigned activities fully comply with regulatory and/or international agencies, such as FDA, ISO, OSHA, EPA, among others.
Participate in the compilation and review of technical documentation for both domestic and international regulatory submissions.
Participate in external audits such as: FDA, Notified Body (BSI), and Corporate, among others.
Performs other related duties as necessary.
Qualifications:
BS in Engineering, preferably Mechanical, Industrial, Electrical, Chemical, or Biomedical (Professional Engineer License.) or science-related field.
Minimum of 4-6 years of experience in the medical device and/or pharmaceutical manufacturing environment.
Lean/Six Sigma . or Black Belt Certification is a plus.
Experience in validations such as manufacturing equipment, manufacturing processes, stability or aging, is required.
Knowledge of FDA, OSHA, EPA, and GMP's and ISO requirements.
Knowledge in Organizational Excellence and Lean/Six Sigma.
Strong Project Management skills.
Ability to lead teams through complex projects and provide departmental technical leadership.
Must have excellent communication skills and a strong track record of working cross-functionally.
Must have demonstrated ability to think strategically. Able to develop technical documentation such as: Change Controls, Validation Plans, Validation Protocols, Technical/investigation reports, SOP, and others. Teamwork-oriented and self-starter.
Source : eTeam Inc.