Manufacturing Process Engineer II at Abbott

Westfield, Indiana, United States

Apply Now

Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Healthcare, Medical DevicesIndustries

Requirements

Develops processes based on product specifications and in consideration to process and test method capabilities
Evaluates process and design alternatives based on Design for Manufacturability (DFM) principles
Uses problem solving and statistical tools and make sound design recommendations
Manages program compliance with Quality requirements (i.e. Design Control, Process validation etc.)
Can identify work environment issues (i.e. OSHA regulations, etc.)
Supports all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements
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
Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures

Responsibilities

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
Conducts tests, collects and formats data, and assists in analysis of engineering studies (DOEs)
Assists in 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
Works to reduce costs in all areas of manufacturing by analyzing current equipment for process suitability and provides detailed plans for improvement
Creates and revises manufacturing documents, specifications, standard operating procedures (SOPs), safety instructions, validation protocols, risk assessments, and procedures and other technical documents to insure compliant, efficient, and safe processes
Conducts preventative maintenance audits and compliance with SOPs, ISO, FDA and cGMP requirements
Researches engineering solutions to a diverse set of challenges in production and development

Skills

Process Development

Manufacturing Equipment

Process Improvement

Cost Reduction

Material Processing

Equipment Optimization

New Product Design

Product Specifications

Abbott

Healthcare solutions in diagnostics and devices

About Abbott

Abbott Laboratories focuses on improving health through various medical technologies and health solutions. The company operates in areas such as cardiovascular health, diabetes management, diagnostic testing, nutrition, and neuromodulation for chronic pain and movement disorders. Abbott's products include advanced medical devices and diagnostic tests that help healthcare professionals and patients manage health conditions effectively. For example, their cardiovascular technologies assist in heart health management, while diabetes care products enable accurate glucose monitoring without painful fingersticks. Unlike many competitors, Abbott emphasizes accessibility and affordability in its offerings, aiming to make life-changing technologies available to a broader audience. The company's goal is to positively impact global health and well-being, supported by a commitment to sustainability and a 2030 Sustainability Plan.

Lake Bluff, IllinoisHeadquarters

1888Year Founded

IPOCompany Stage

HealthcareIndustries

10,001+Employees