Manufacturing Engineer

Manufacturing Engineer at Codon Partners Manufacturing Engineer at Codon Partners in Lahaska, Pennsylvania Posted in 2 days ago.

Type:

full-time

Job Description:

Manufacturing Engineer (Contract)

Location:

Doylestown, PA (Onsite)

Duration:

3-6

Month Contract Schedule:

40 Hours per Week Position Overview 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. Responsibilities 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. Participate in investigations, corrective actions, and continuous improvement activities as assigned. Support validation and qualification documentation efforts. Track action items and provide administrative support for engineering projects. Perform other manufacturing engineering support activities as needed. Qualifications Required 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. Strong organizational skills and attention to detail. Ability to manage multiple priorities and work independently. Preferred 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. Key Attributes Detail-oriented and highly organized. Strong written communication skills. Comfortable handling documentation-heavy assignments. Collaborative team player who can work effectively with manufacturing, quality, and engineering personnel. Eager to learn and develop within a manufacturing engineering environment.