Staff Quality Engineer, ECMP Workstream Leader

Changing lives. Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care. The Staff Quality Engineer, ECMP Work stream Leader is a key role within the Enterprise Compliance Master Plan (ECMP), having the responsibility of leading Change Control Work stream, which includes lifecycle management for product changes, and document controls for design and process documentation of the Quality Management System (QMS). This role will be responsible for leading a team of individuals and partnering with global quality leaders to develop processes that result in attaining the company's improvement objectives and growth strategies across more than 15 design, manufacturing, and distribution facilities and a diverse portfolio of leading medical devices. This role is crucial for ensuring the development, manufacture, and distribution of medical devices in compliance with corporate policies, U.S. Food and Drug Administration regulations, ISO 13485, the Canadian Medical Device Regulations (CMDR), the EU Medical Device Regulation, Japanese Pharmaceutical Affairs Law, and other applicable regulatory agencies.

RESPONSIBILITIES

Drive standardization & deploy world-class solutions to drive improved quality and compliance. Recognized as a leading expert and internal thought leader in the designated QMS area with high-level knowledge and broad, comprehensive knowledge of other QMS disciplines. Leads major improvements to existing processes and develops or champions new systems, concepts, and procedures to solve unique and complex problems that have a broad impact on the business. Evaluate new regulations, guidelines and industry standards and their impact on

ECMP QMS

Workstream processes; plan and effectively implement plans across the business to maintain compliance. Establish a global community of practice for the designated QMS area or collaborate with responsible people to enhance the existing community of practice, including governance and oversight, to ensure compliance and consistency in relevant sub-processes applicable to the designated QMS area. Collaborate with process owners and stakeholders in corporate, divisions and sites to ensure the program is compliant, executable, and meets user needs. Ensure compliance of all process and digital improvements with all appropriate regulations and standards, including

FDA, ISO 13485, CMDR, EU

MDR and PMD Act. Interact and coordinate activities with other departments, external vendors, and customers. Influences and collaborates across stakeholder groups in the areas of process / system improvements, identify and implement opportunities. - Drive quality culture improvements and foster collaboration to ensure functional teams work harmoniously and secure synergy and strengths across the global teams. Provides strategic direction and communication of the

ECMP QMS

work stream goals, directives, and policies to employees, creating a clear vision and positive, team-oriented environment resulting in the achievement of the company's goals and increased profitability. Demonstrates technical leadership as an inter-departmental resource coaching and teaching other Integra Leaders across all functions and geographies. Perform other related duties as expected.

QUALIFICATIONS

Bachelor's Degree in Engineering, or Sciences or relevant Technical Field required. Master's degree preferred. Minimum 10 years of experience in quality, manufacturing, or engineering, or equivalent education and years of experience Strong experience leading deployment of enterprise quality management solutions Experience in FDA controlled environment. Strong collaboration and facilitation skills and experience working in a matrix environment. Ability to interface with technical and non-technical personnel. Knowledge of

FDA QMSR, ISO, MDSAP, EU MDR, PMD

Act and other applicable standards and regulations. This position could require up to 50% travel.

PHYSICAL REQUIREMENTS

The physical requirements listed in this section include, but are not limited, to the motor/physical abilities and skills require of position in order to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position.

ADVERSE WORKING CONDITIONS

There are no adverse working conditions associated with this position.

Salary Pay Range:

$109,250.00 - $149,500.00 USD Salary Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training. In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. Additional Description for

Pay Transparency:

Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)). Subject to the terms of their respective policies and date of hire, Employees are eligible for the following https://jobs.integralife.com/total-rewards/ 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'd like more information on your rights under the law, please see the following notices: EEO Is the Law | EOE including Disability/Protected Veterans 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. If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com. Unsolicited Agency Submission Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate's name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails. Integra - Employer Branding from Integra LifeSciences on Vimeo Changing Lives. Building Careers. Integra LifeSciences, a world leader in medical technology, is dedicated to limiting uncertainty for surgeons, so they can concentrate on providing the best patient care. Integra offers innovative solutions in neurosurgery, reconstructive and general surgery, and regenerative wound care. Founded in 1989 Integra is headquartered in Princeton, New Jersey and has more than 4,000 employees worldwide. Integra's common stock is listed on The NASDAQ Stock Market under the symbol "IART."