Manufacturing Process Engineer I

Abbott; United States; On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health insurance

Retirement plan

Tuition reimbursement

Education benefits

Job summary

Abbott in Scarborough, ME, invites applications for a Manufacturing Process Engineer I to manage manufacturing equipment and cost-saving initiatives, improve efficiency, and support new product design. The role focuses on process improvement, equipment validation, and adherence to quality systems.

The position requires a BS in Engineering, familiarity with cGMP and ISO 13485, and experience in mechanical/biomedical engineering.

Qualifications

• Bachelor's degree in Engineering or equivalent combination of education and experience.
• Familiarity with cGMP and ISO 13485 regulations and practices.
• Exposure to mechanical, biomedical, industrial or chemical engineering.
• Knowledge of engineering principles, methodologies and industry standards.

Responsibilities

• Carries out duties in compliance with established business policies and procedures.
• Assists in designing or developing new manufacturing processes and equipment and assists in process verification and validation.
• Conduct tests, collect and format data, and assist in analysis of engineering studies (DOEs).
• Assists in the start-up of new equipment and execution of validation protocols.
• Maintains positive and cooperative communications with all levels of employees, customers, contractors, and vendors.

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:

• Career development with an international company where you can grow the career you dream of.
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with a high employer contribution.
• Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
• A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

The Manufacturing Process Engineer I works out of our Scarborough, ME location in the Infectious Disease , Diagnostics Division. We're empowering smarter medical and economic decision-making to help transform the way people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott's diagnostics instruments, providing lab results for millions of people.

The Manufacturing Process Engineer I will be responsible for all Manufacturing Equipment and equipment quality/cost savings initiatives, improving efficiency through material and process improvement, reducing material processing costs, and participating in new product design.

What You'll Work On

• Carries out duties in compliance with established business policies and procedures.
• Demonstrates commitment to the development, implementation and effectiveness of applicable Quality Processes as per ISO, FDA, and other regulatory agencies.
• Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices.
• Responsibility to understand and maintain awareness of the quality consequences which may occur from the improper performance of their specific job.
• Support department by performing related tasks as requested.
• Assists in designing or developing new manufacturing processes and equipment and assists in process verification and validation.
• Conduct tests, collect and format data, and assist in analysis of engineering studies (DOEs).
• Assists in the start-up of new equipment and execution of validation protocols.
• Participates in technical design reviews for process equipment and product design and requirements documents.
• Responsible for utilizing and maintaining the effectiveness of the quality system, including supporting Quality Incidents and CAPA investigations and actions.
• Analyzes raw material specifications to ensure appropriate features and limits are in place to support company manufacturing process.
• Evaluates company initiated raw material changes and coordinates appropriate testing and validation as required.
• Suggests and supports new methods or materials for continual improvement and optimization in the quality or efficiency of a product or process.
• Creates and revises manufacturing documents, specifications, standard operating procedures (SOPs), safety instructions, validation protocols, risk assessments, and other technical documents to ensure compliant, efficient, and safe processes.
• Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
• Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

Required Qualifications

• Bachelor's degree (BS) in Engineering or equivalent combination of education and experience.
• Familiarity with cGMP and ISO 13485 regulations and practices.
• Exposure to mechanical, biomedical, industrial or chemical engineering.
• Knowledge of engineering principles, methodologies and industry standards.

PREFERRED QUALIFICATIONS:

• Prior experience working in a company operating under ISO, FDA, or similar quality systems or regulations.
• Exposure to cGMP and ISO 13485 regulations and practices.
• Experience in Microsoft Suites software. (Excel, PowerPoint, Power BI, etc.).
• Exposure to statistical analysis software. (Minitab or JMP preferred).

COMPETENCIES:

General Competencies:

• Multitasking: Demonstrates the ability to handle multiple tasks or responsibilities simultaneously