Engineering Project Manager

INTEGRA LIFESCIENCES CORP; Cincinnati (OH); On-site; USD 62,000 - 85,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401(k) savings plan

Disability coverage

Job summary

Integra LifeSciences Corp seeks an Engineering Project Manager to provide technical leadership for site facilities, utilities, equipment, and capital projects across manufacturing, laboratory, and non‑manufacturing spaces.

The role leads multidisciplinary project definition through hand‑off, including validation/commissioning, to optimize asset lifecycle management and sustainability while maintaining compliance with FDA, GMP, ISO 9001/13485, EU MDR, CMDR, and other regulatory standards.

Qualifications

• Bachelor’s degree in Engineering or a related field with 5+ years leading projects.
• Strong organizational and communication skills.
• Experience in a regulated manufacturing environment.

Responsibilities

• Lead site engineering projects across manufacturing and labs.
• Supervise engineers and technicians; manage scheduling and training.
• Support ECOs, CAPAs, FMEA, IQ/OQ/PQ validations.
• Ensure regulatory compliance and safety.

Skills

Project leadership

Engineering degree

Communication skills

Regulated manufacturing experience

Education

Bachelor’s degree in Engineering

Master’s degree in Engineering

Tools

Microsoft Office

Data analysis tools

Job description

Overview

The Engineering Project Manager is responsible for the technical and leadership of Integra’s site facilities, utilities, equipment, and capital projects across manufacturing, laboratory, and non‑manufacturing spaces. They lead multidisciplinary project definition through hand‑off, including validation/commissioning, to optimize asset lifecycle management and sustainability while maintaining compliance with corporate policies and regulatory standards (FDA, GMP, ISO 9001/13485, EU MDR, CMDR, etc.).

Key Responsibilities

• Promote a strong culture of safety by actively supporting environmental, health, and safety (EHS) programs.
• Ensure team compliance with safety procedures, PPE usage, permits, housekeeping, and hazard awareness.
• Participate in accident, near‑miss, and incident investigations and support corrective actions.
• Manage and execute site engineering projects, including product and process transfers, equipment qualifications, process validations, efficiency improvements, and resolution of quality and supply issues.
• Supervise and support a team of engineers and technicians, including scheduling, training, daily operations coordination across shifts, and addressing operational challenges.
• Contribute to performance management, employee development, and reporting of team results.
• Support development and execution of engineering deliverables such as process requirements, specifications, drawings, engineering change orders (ECOs), CAPAs, and risk assessments (e.g., FMEA), as well as validation activities (IQ, OQ, PQ, PV, TMV, etc.).
• Ensure project activities align with regulatory and quality requirements to maintain the safety, effectiveness, and reliability of medical devices with a focus on patient safety.
• Track and execute projects against defined timelines, budgets, and performance targets, supporting productivity and capital plan objectives for manufacturing and process equipment.
• Collaborate with cross‑functional teams and external contractors to implement projects, select equipment, and support facility or process improvements.
• Monitor contractor progress against schedules, deliverables, and change controls; assist in documentation and handover activities, including as‑built drawings and project records.
• Perform other related duties as assigned.

Skills & Competencies

• Bachelor’s degree in Engineering or a technical field with 5+ years of experience, including some leadership of projects or direct reports; or Master’s degree with 3+ years of relevant experience.
• Strong organizational and communication skills (written and verbal).
• Working knowledge of financial considerations related to projects, including budgets and cost impact of improvements.
• Proficiency in Microsoft Office and familiarity with data analysis or statistical tools.
• Experience in a regulated manufacturing environment (medical device or pharmaceutical preferred).
• Basic knowledge of health, safety, and environmental regulations.
• Self‑motivated team player with the ability to work effectively both independently and collaboratively across functions.

Salary

Salary: $62,000.00 – $85,000.00 USD. Salary ranges are determined by role, level, and location and may be supplemented by bonus, commission, equity, or other variable compensation.

Benefits

Employees and/or eligible dependents are eligible to participate in the following company‑sponsored benefit programs, subject to the terms of their respective plans: medical, dental, vision, life insurance, short‑ and long‑term disability, business accident insurance, group legal insurance, and a savings plan (401(k)).

EEO & ADA Statement

Integra LifeSciences is an equal opportunity employer and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status. This site is governed solely by applicable U.S. laws and governmental regulations.

If you have a disability and need an accommodation for the application process, please email us at [e-mail]. Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA.