Engineer II Process – Controls

Abbott; Liberty Township (OH); On-site; USD 61,000 - 123,000; Full time

Job summary

Abbott, a global healthcare leader, is seeking a qualified engineer for manufacturing design and process development in the United States. The role involves creating design specifications, evaluating manufacturability, and ensuring compliance with regulatory standards including FDA requirements.

Responsibilities include establishing manufacturing processes, analyzing design alternatives, and maintaining knowledge of new manufacturing technologies.

Qualifications

• Bachelor's degree in engineering or a technical field.
• Minimum 2 years of experience.
• 2–4 years of manufacturing experience; experience designing and testing medical devices; experience developing manufacturing processes and designing for manufacturability.

Responsibilities

• Establishes processes based on product specifications.
• Evaluates process and design alternatives based on design for manufacturability.
• Understands principles of Cost of Goods Sold (COGS).
• Manages program compliance with Quality Control requirements (Design Control, Process validation).
• Maintains knowledge of new developments in manufacturing and design technologies.
• Understand work environment issues (OSHA).
• Supports company initiatives in QMS, EMS, and other regulatory requirements.
• Complies with FDA regulations and other regulatory requirements; maintains communication with all levels of employees, customers, contractors and vendors.

Skills

Design analysis

Manufacturing processes

Quality systems

Regulatory compliance

Cross-functional collaboration

Education

Bachelor's degree in Engineering or Technical Field

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 115,000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:

MAIN PURPOSE OF ROLE

• Performs analyses to develop design specifications and performance requirements. Provides technical information concerning manufacturing or processing techniques, materials, properties and process (advantages/limitations) engineering planning. Selects techniques to solve problems and make sound design recommendations.

MAIN RESPONSIBILITIES

Establishes processes based on product specifications.

Evaluates process and design alternatives based on “design for manufacturability” principles.

Understands principles of “Cost of Goods Sold”.

Manages program compliance with “Quality Control” requirements (i.e. Design Control, Process validation etc.).

Maintains knowledge of new developments in manufacturing and design technologies.

Understand work environment issues (i.e. OSHA regulations, etc.).

Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.

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.

QUALIFICATIONS

Education

• BachelorsDegree (±16 years)

-Engineering or Technical Field

Experience/Background

• Minimum 2 years

-2–4 years manufacturing experience. Experience designing and testing medical devices required. Experience developing manufacturing processes and technologies and designing for manufacturability required.

-Experience working in a broader enterprise/cross-division business unit model preferred. Ability to work in a highly matrixed and geographically diverse business environment. Ability to work within a team and as an individual contributor in a fast-paced, changing environment. Ability to leverage and/or engage others to accomplish projects. Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization. Multitasks, prioritizes and meets deadlines in timely manner. Strong organizational and follow-up skills, as well as attention to detail.

-Ability to travel, including internationally.

The base pay for this position is

$61,300.00 – $122,700.00

In specific locations, the pay range may vary from the range posted.

LOCATION:

United States > Liberty : 253 Financial Blvd.

WORK SHIFT:

Standard

TRAVEL:

No

MEDICAL SURVEILLANCE:

No

SIGNIFICANT WORK ACTIVITIES:

Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day)

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf

EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

Abbott is a global healthcare leader enhancing lives through innovative diagnostics, medical devices, nutrition, and branded generic medicines across more than 160 countries.