Manufacturing engineering - systems

Manufacturing Engineer (Contract)
Duration: 3-6 Month Contract
Our client, a growing medical device manufacturer, is seeking a Manufacturing Engineer for a 3-6 month onsite contract assignment in Doylestown, PA. This role will support manufacturing and engineering operations through documentation updates, process improvements, engineering change activities, and day-to-day administrative support of manufacturing engineering projects.
This opportunity is ideal for an early-career Manufacturing Engineer who has gained hands-on experience in a regulated manufacturing environment and is looking to further develop their engineering and quality systems knowledge.

Create, revise, and maintain manufacturing documentation, including work instructions, procedures, manufacturing travelers, and forms.
Support Engineering Change Orders (ECOs) and document control activities.
Assist with updating Device History Records (DHRs), Device Master Records (DMRs), and related manufacturing documentation.
Collaborate with manufacturing, quality, and engineering teams to ensure documentation accuracy and compliance.
Support process improvement initiatives by gathering data, documenting current-state processes, and assisting with implementation activities.
Maintain engineering records and organize project documentation.
Assist with equipment, tooling, and manufacturing process documentation.
Track action items and provide administrative support for engineering projects.
Perform other manufacturing engineering support activities as needed.

Bachelor's degree in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, Biomedical Engineering, or a related technical discipline.

• 1-5 years of manufacturing engineering experience.
• Strong technical writing and documentation skills.
• Experience working in a manufacturing environment.
• Proficiency with Microsoft Office applications, particularly Excel and Word.
• Experience in medical device, pharmaceutical, biotech, or other regulated manufacturing industries.

Familiarity with GMP, FDA, ISO 13485, or quality management systems.
Exposure to document control systems and engineering change processes.
Experience supporting validation, quality, or process improvement projects.
Knowledge of Lean Manufacturing or continuous improvement methodologies.
Collaborative team player who can work effectively with manufacturing, quality, and engineering personnel.
Eager to learn and develop within a manufacturing engineering environment.